Upload
others
View
9
Download
0
Embed Size (px)
Citation preview
Sulfonyl ChloridesUsed for the introduction of the sulfonyl functional group in the parallel synthesis of sulfonamides, sulfonates, and similar derivatives, these and many other sulfonyl chlorides are regularly manufactured at our laboratories. An extensive range of sulfonyl chlorides is listed along with over 46,000 other products in the complete Alfa Aesar catalog.
Find out more at alfa.com
For Research Use Only. Not for use in diagnostic procedures. © 2019 Thermo Fisher Scientific Inc. All rights reserved. All trademarks are the property of Thermo Fisher Scientific and its subsidiaries unless otherwise specified.
A152633,4-Dimethoxybenzenesulfonyl chloride, 98%
[23095-31-0]
B244164-Iodobenzenesulfonyl chloride, 97%
[98-61-3]
B229873-(Chlorosulfonyl)benzoic acid, 97%
[4025-64-3]
A131403-Fluorobenzenesulfonyl chloride, 98%
[701-27-9]
B216324-Chloro-3-nitrobenzenesulfonyl chloride,
98%[97-08-5]
A143625-Chloro-2-methoxybenzenesulfonyl
chloride, 98% [22952-32-5]
B24250Naphthalene-1-sulfonyl chloride, 98%
[85-46-1]
A15553Thiophene-2-sulfonyl chloride, 97%
[16629-19-9]
A117795-Chloro-4-nitrothiophene-2-sulfonyl
chloride, 98% [58457-24-2]
B204113,5-Dimethylisoxazole-4-sulfonyl chloride,
98%[80466-79-1]
SO2Cl
OCH3
Cl
S SO2Cl
O2N
Cl
ON
CH3ClSO2
CH3
Grignard Reagents in 2-MeTHFThe Alfa Aesar brand offers Grignard reagents in 2-Methyltetrahydrofuran (2-MeTHF), a cost-effective, green alternative to Tetrahydrofuran.
2-MeTHF is derived from renewable resources such as corn cobs and oat hulls, and is capable of producing high concentrations of bromo, benzyl and allyl Grignard reagents. The higher boiling point of 2-MeTHF (80°C) versus THF (66°C) allows for higher reaction temperatures, reducing loss of solvent. 2-MeTHF quickly produces clean water phase splits without forming emulsions. Unlike THF, it is very stable even in highly acidic environments, and it forms an effective azeotrope with water. Given these properties of 2-MeTHF, this range of Grignard reagents will allow easier processing and work up.
Find out more at alfa.com
For Research Use Only. Not for use in diagnostic procedures. © 2019 Thermo Fisher Scientific Inc. All rights reserved. All trademarks are the property of Thermo Fisher Scientific and its subsidiaries unless otherwise specified.
H51154Benzylmagnesium chloride,
1M in 2-MeTHFCAS 6921-34-2
H511613-Chlorophenylmagnesium bromide,
1M in 2-MeTHFCAS 36229-42-2
H511634-Chlorophenylmagnesium bromide,
1M in 2-MeTHF CAS 873-77-8
H51165Cyclohexylmagnesium chloride,
1M in 2-MeTHFCAS 931-51-1
H51166Cyclopentylmagnesium chloride,
1M in 2-MeTHFCAS 32916-51-1
H511683-Fluorophenylmagnesium bromide,
1M in 2-MeTHFCAS 17318-03-5
H511694-Fluorophenylmagnesium bromide,
1M in 2-MeTHF CAS 352-13-6
H511591-Naphthylmagnesium bromide,
0.5M in 2-MeTHF CAS 703-55-9
H511602-Naphthylmagnesium bromide,
0.25M in 2-MeTHF CAS 21473-01-8
MgCl
CH2MgCl Cl MgBr MgBr
Cl
MgClF MgBr
MgBr
F
MgBrMgBr
Click Chemisty ReagentsThe Alfa Aesar brand offers a selection of compounds for use in click chemistry reactions. Click chemistry is a newer approach to synthesis that makes use of simple, rapid and reliable reactions. It has several benefits over other synthesis approaches such as being orthogonal to conventional methods and occurring under relatively mild conditions. These reactions also proceed with high, almost quantitative, yields. These benefits have made click chemistry reactions a popular method of introducing labels and other tags to biomolecules. The most popular click chemistry reaction is the Huisgen 1,3-dipolar cycloaddition of alkynes to azides, which is generally carried out with catalysis by copper (I), or by introduction of an azide to a strain-promoted cyclooctyne. The following is a selection of bifunctional linkers, fluorescent tags and chemical modifications that can be used with the azide-alkyne click chemistry technique.
Find out more at alfa.com
For Research Use Only. Not for use in diagnostic procedures. © 2019 Thermo Fisher Scientific Inc. All rights reserved. All trademarks are the property of Thermo Fisher Scientific and its subsidiaries unless otherwise specified.
N
O
COOH N
O
NH2 N
O
NH
OO
OO
O
H2N
J64308
1-Amino-11-azido-3,6,9-trioxaundecane
J64030
15-Azido-4,7,10,13-tetraoxapentadecanoic
acid
J64834
N-Succinimidyl 15-azido-4,7,10,13-
tetraoxapentadecanoate
J64256
Azadibenzocyclooctyne-S-S-PEG3-
biotin conjugate
J64671
Azadibenzocyclooctyne-sulfobiotin
conjugate
J65570
Azadibenzocyclooctyne-PEG4-
phorphoramidite
J64617
Azadibenzocyclooctyne-PEG4-alcohol
J65377
Azadibenzocyclooctyne-maleimide
J65673
Azadibenzocyclooctyne-maleimide
J64549
Azadibenzocyclooctyne acid
J65637
Azadibenzocyclooctyne-amine
J65301
Azadibenzocyclooctyne-PEG4 amine
N
O
NH
OO
OO
O
HO
N
O
NH
N
O
O
ON
O
NH
OO
O
ONH
O
O
N
O
O
O
N
HN
SS
HN
O
OO
O OHN
OS
HN
NH
O
H
H
N
O
NH
NH
O
S
HN NH
H H
O
SO3
O
(CH3CH2CH2)3N+
N
OHN
OO
O
OO
PO
N[CH(CH3)2]2
NC
N3
OO
OO
O
O N
O
O
COOHO
OO
ON3H2N
OO
ON3
Click Chemisty Reagents
Find out more at alfa.com
For Research Use Only. Not for use in diagnostic procedures. © 2019 Thermo Fisher Scientific Inc. All rights reserved. All trademarks are the property of Thermo Fisher Scientific and its subsidiaries unless otherwise specified.
S
HN
NH
O
H
H
NH
O
OO
O
N3
S
HN
NH
O
H
H
NH
O
O
O
OO
OO
O
OO
OO
N3
OH2N NH2
COO
NH
OO
O
N3
O
J65476
Azido-PEG3-sulforhodamine 101 conjugate
J65668
3-Azido-1-propylamine
J64527
1-Amino-3,6,9,12-tetraoxapentadec-14-yne
J64902
N-Succinimidyl 4,7,10,13,16-
pentaoxanonadec-18-ynoate
J64859
Acetylene-PEG4-maleimide
J65577
Acetylene-PEG4-biotin conjugate
J65529
Azido-PEG3-sulforhodamine B conjugate
J65984
Azido-PEG3-maleimide kit
J64510
Azido-PEG3-carboxytetramethylrhodamine
110 conjugate
J64996
3-Azido-PEG3-biotin conjugate
J65147
Azido-PEG11-biotin conjugate
J65107
Azido-PEG3-carboxyrhodamine 110
conjugate
O(CH3CH2)2N N(CH2CH3)2
SO3
SNH
OO
O
N3
OO
ONH
N
O
O
O
OO
N3 O(CH3)2N N(CH3)2
COO
NH
OO
O
N3
O
ON N
SO3
SNH
OO
O
N3
OO
NH2N3 OO
OO
H2N
OO
O
O N
O
O
O
OO
ONH
N
O
O
O
O
OO
S
HN
NH
O
H
H
NH
O
O
OO
O
Boronic Acids
Find out more at alfa.com
For Research Use Only. Not for use in diagnostic procedures. © 2019 Thermo Fisher Scientific Inc. All rights reserved. All trademarks are the property of Thermo Fisher Scientific and its subsidiaries unless otherwise specified.
H52542
boronic acid, 97%
[833472-82-5]
H52536
[874219-56-4]
L17485
boronic acid, 97%
[166316-48-9]
H31156
2-Cyclohexylethylboronic acid pinacol
ester, 96%
[167692-95-7]
H30441
1-Propylboronic acid pinacol ester, 98%
[67562-19-0]
H26254
[411235-57-9]
H55723
acid, 97%
[28611-39-4]
B22922
acid, 97%
[1582-24-7]
H64100
acid, 97%
[819849-20-2]
H52467
acid, 97%
[91983-14-1]
H55857
acid, 97%
[851135-07-4]
H52965
acid, 98%
[192182-54-0]
Alkylboronic acids and esters
Arylboronic acids
BO
O
CH3
CH3
CH3
CH3
CH3
BO
O
CH3
CH3
CH3
CH3
B(OH) 2
B(OH) 2
(CH3)2N
B(OH) 2
F
F
F
F
F
B(OH) 2
F
O2N
B(OH) 2
CH2Br
B(OH) 2
FHOOC
B(OH) 2CH3O
OCH3
B(OH) 2CH3OCOCH2CH2
B(OH) 2O2N
NHCOOCH2Ph
B(OH) 2
HOOCCH2CH2
Boronic Acids
Find out more at alfa.com
For Research Use Only. Not for use in diagnostic procedures. © 2019 Thermo Fisher Scientific Inc. All rights reserved. All trademarks are the property of Thermo Fisher Scientific and its subsidiaries unless otherwise specified.
L19763
[143314-16-3]
L13538
[105832-38-0]
H55315
[456-27-9]
H59738
2-Fluoro-4-(methoxycarbonylmethyl)-
[1259022-70-2]
H51123
boronic acid
[302348-51-2]
H59126
acid, 96%
[1165936-03-7]
H32674
95%
[910251-11-5]
L17967
97%
[374564-35-9]
H52588
Potassium 4-(methoxycarbonyl)-
[705254-34-8]
H59194
boronic acid pinacol ester, 96%
[1256256-45-7]
H51955
acid bis(pinacol) ester, 95%
[196207-58-6]
H62654
boronic acid pinacol ester, 96%
[939968-08-8]
Aryltri�uoroborate and tetra�uoroborate salts
Arylboronic esters
BO
O
CH3 CH3
CH3
CH3
F(CH3)3COCONH
B
O
OCH3
CH3
CH3CH3CH3(CH2)7 (CH2)7CH3
B
O
OCH3
CH3
CH3CH3
BO
O
CH3 CH3
CH3
CH3
F
H2N
F
BO
O
CH3 CH3
CH3
CH3
FCH3OCOCH2
BO
O
CH3
CH3
CH3
CH3
HOCH2
BO
O
CH3 CH3
CH3
CH3
FCH3
CH3O BF3K
BF3K
Br
BF3K
CH3OCO
N
O
O
O
N(CH3)2
N(CH3)2BF4
+-
CH3O
N2+
BF4N
N
CH2CH3
CH3
BF4
Cyclopropane DerivativesThe following reactive cyclopropanes are a selection of our current listings.
Find out more at alfa.com
For Research Use Only. Not for use in diagnostic procedures. © 2019 Thermo Fisher Scientific Inc. All rights reserved. All trademarks are the property of Thermo Fisher Scientific and its subsidiaries unless otherwise specified.
A13540Cyclopropyl methyl ketone, 99%
[765-43-5]
B25102Cyclopropyltriphenylphosphonium
bromide, 98% [4114-05-7]
H320832,2-Di�uorocyclopropanemethanol, 97%
[509072-57-5]
H26254Cyclopropylboronic acid, tech. 85%
[411235-57-9]
L179571-Tri�uoromethylcyclopropane-1-
carboxylic acid, 97% [277756-46-4]
H510784-Cyclopropyl-4-oxobutyric acid, 95%
[53712-75-7]
H26902(R)-1-Cyclopropylethylamine, ChiPris®,
98%, ee 98+% [6240-96-6]
H275251-Phenylcyclopropanecarboxylic acid, 97%
[6120-95-2]
H26273Cyclopropylmagnesium bromide,
ca 0.5M in THF [23719-80-4]
Organic Intermediates
Find out more at alfa.com
For Research Use Only. Not for use in diagnostic procedures. © 2019 Thermo Fisher Scientific Inc. All rights reserved. All trademarks are the property of Thermo Fisher Scientific and its subsidiaries unless otherwise specified.
F
F
(CH3)3CCH2COCl CH2Br
O O
C C
Cl Cl Ph2BOCH2CH2NH2
O
O
O
CH3
H2N(CH2)3
CH3
Si
CH3
O
CH3
Si
CH3
(CH2)3NH2
(CH3)2CHCH2
H2N
H
CH2OH
F
F
(CH3)3CCH2COCl CH2Br
O O
C C
Cl Cl Ph2BOCH2CH2NH2
O
O
O
CH3
H2N(CH2)3
CH3
Si
CH3
O
CH3
Si
CH3
(CH2)3NH2
(CH3)2CHCH2
H2N
H
CH2OH
F
F
(CH3)3CCH2COCl CH2Br
O O
C C
Cl Cl Ph2BOCH2CH2NH2
O
O
O
CH3
H2N(CH2)3
CH3
Si
CH3
O
CH3
Si
CH3
(CH2)3NH2
(CH3)2CHCH2
H2N
H
CH2OH
$
N CH2Cl
.HCl
NHCOCH3
CH3O
CO2H
CH2=CHCH2 CH
CO2H
Ph3P=CHCHO
N
O2N N CH3
CH2CH2OH
CH3
CH3 NN
COCH2CN
CH3
Br NO2
COCH3
Br
OH
NH2 .HCl
$
N CH2Cl
.HCl
NHCOCH3
CH3O
CO2H
CH2=CHCH2 CH
CO2H
Ph3P=CHCHO
N
O2N N CH3
CH2CH2OH
CH3
CH3 NN
COCH2CN
CH3
Br NO2
COCH3
Br
OH
NH2 .HCl
A10377 1,2-Difluorobenzene, 98+%
CAS: 367-11-3
A18012 Oxalyl chloride, 98%
CAS: 79-37
B20890 2-Methyltetrahydrofuran-3-one, 98+%
CAS: 3188-00-9
A10226 2-(Chloromethyl)pyridine hydrochloride, 98%
CAS: 6959-47-3
A11709 (Formylmethylene)triphenyl phosphorane
CAS: 2136-75-6
F
F
(CH3)3CCH2COCl CH2Br
O O
C C
Cl Cl Ph2BOCH2CH2NH2
O
O
O
CH3
H2N(CH2)3
CH3
Si
CH3
O
CH3
Si
CH3
(CH2)3NH2
(CH3)2CHCH2
H2N
H
CH2OH
F
F
(CH3)3CCH2COCl CH2Br
O O
C C
Cl Cl Ph2BOCH2CH2NH2
O
O
O
CH3
H2N(CH2)3
CH3
Si
CH3
O
CH3
Si
CH3
(CH2)3NH2
(CH3)2CHCH2
H2N
H
CH2OH
F
F
(CH3)3CCH2COCl CH2Br
O O
C C
Cl Cl Ph2BOCH2CH2NH2
O
O
O
CH3
H2N(CH2)3
CH3
Si
CH3
O
CH3
Si
CH3
(CH2)3NH2
(CH3)2CHCH2
H2N
H
CH2OH
$
N CH2Cl
.HCl
NHCOCH3
CH3O
CO2H
CH2=CHCH2 CH
CO2H
Ph3P=CHCHO
N
O2N N CH3
CH2CH2OH
CH3
CH3 NN
COCH2CN
CH3
Br NO2
COCH3
Br
OH
NH2 .HCl
$
N CH2Cl
.HCl
NHCOCH3
CH3O
CO2H
CH2=CHCH2 CH
CO2H
Ph3P=CHCHO
N
O2N N CH3
CH2CH2OH
CH3
CH3 NN
COCH2CN
CH3
Br NO2
COCH3
Br
OH
NH2 .HCl
A10162 tert-Butylacetyl chloride, 98+%
CAS: 7065-46-5
A10162 2-Aminoethyl diphenyl-borinate, 98%
CAS: 524-95-8
L17295 1,3-Bis(aminopropyl)tetra-methyldisiloxane, 97%
CAS: 2469-55-8
A13253 4’-Methoxyacetanilide, 98+%
CAS: 51-66-1
H60258 Metronidazole, 99%
CAS: 443-48-1
F
F
(CH3)3CCH2COCl CH2Br
O O
C C
Cl Cl Ph2BOCH2CH2NH2
O
O
O
CH3
H2N(CH2)3
CH3
Si
CH3
O
CH3
Si
CH3
(CH2)3NH2
(CH3)2CHCH2
H2N
H
CH2OH
F
F
(CH3)3CCH2COCl CH2Br
O O
C C
Cl Cl Ph2BOCH2CH2NH2
O
O
O
CH3
H2N(CH2)3
CH3
Si
CH3
O
CH3
Si
CH3
(CH2)3NH2
(CH3)2CHCH2
H2N
H
CH2OH
F
F
(CH3)3CCH2COCl CH2Br
O O
C C
Cl Cl Ph2BOCH2CH2NH2
O
O
O
CH3
H2N(CH2)3
CH3
Si
CH3
O
CH3
Si
CH3
(CH2)3NH2
(CH3)2CHCH2
H2N
H
CH2OH
$
N CH2Cl
.HCl
NHCOCH3
CH3O
CO2H
CH2=CHCH2 CH
CO2H
Ph3P=CHCHO
N
O2N N CH3
CH2CH2OH
CH3
CH3 NN
COCH2CN
CH3
Br NO2
COCH3
Br
OH
NH2 .HCl
$
N CH2Cl
.HCl
NHCOCH3
CH3O
CO2H
CH2=CHCH2 CH
CO2H
Ph3P=CHCHO
N
O2N N CH3
CH2CH2OH
CH3
CH3 NN
COCH2CN
CH3
Br NO2
COCH3
Br
OH
NH2 .HCl
A13535 Benzyl bromide, 99%
CAS: 100-39-0
B20911 Cyclooctanone, 98%
CAS: 502-49-8
B23745 L-Leucinol, 97%CAS: 7533-40-6
A17443 Allylmalonic acid, 98+%
CAS: 2583-25-7
L08369 1-Cyanoacetyl-3,5-dimthyl-1H- pyrazole, 97%
CAS: 36140-83-7
Organic Intermediates
Find out more at alfa.com
For Research Use Only. Not for use in diagnostic procedures. © 2019 Thermo Fisher Scientific Inc. All rights reserved. All trademarks are the property of Thermo Fisher Scientific and its subsidiaries unless otherwise specified.
$
N CH2Cl
.HCl
NHCOCH3
CH3O
CO2H
CH2=CHCH2 CH
CO2H
Ph3P=CHCHO
N
O2N N CH3
CH2CH2OH
CH3
CH3 NN
COCH2CN
CH3
Br NO2
COCH3
Br
OH
NH2 .HCl
CN CH2=CH(CH2)3Br
HO
O O
CH3
S
CO2H
CCl3
C
NH
OC(CH3)3
H(OCH2CH2)6OH
CH2CH2OH
(CH3)3COOCCH=PPH3
CH3
CH3
CH3
CH3
O
O
B
O
CH3
CN CH2=CH(CH2)3Br
HO
O O
CH3
S
CO2H
CCl3
C
NH
OC(CH3)3
H(OCH2CH2)6OH
CH2CH2OH
(CH3)3COOCCH=PPH3
CH3
CH3
CH3
CH3
O
O
B
O
CH3
CN CH2=CH(CH2)3Br
HO
O O
CH3
S
CO2H
CCl3
C
NH
OC(CH3)3
H(OCH2CH2)6OH
CH2CH2OH
(CH3)3COOCCH=PPH3
CH3
CH3
CH3
CH3
O
O
B
O
CH3
A12951 4-Bromo-2-nitrotoluene, 99%
CAS: 60956-26-5
A10309 Cyclobutanecarbonitrile, 97%
CAS: 4426-11-3
A17737 5-Methylthiophene-2-carboxylic acid, 98+%
CAS: 1918-79-2
L11080 2-Cyclopropylethanol, 96%
CAS: 2566-44-1
$
N CH2Cl
.HCl
NHCOCH3
CH3O
CO2H
CH2=CHCH2 CH
CO2H
Ph3P=CHCHO
N
O2N N CH3
CH2CH2OH
CH3
CH3 NN
COCH2CN
CH3
Br NO2
COCH3
Br
OH
NH2 .HCl
A11982 2’-Bromoacetophenone, 99%
CAS: 2142-69-0
A11219 5-Bromo-1-pentene, 96%
CAS: 1119-51-3
B22039 tert-Butyl 2,2,2-trichloro- acetimidate, 97%
CAS: 98946-18-0
L15144 (tert-Butoxycarbonylmethylene)
triphenylphosphorane, 98% CAS: 35000-38-5
$
N CH2Cl
.HCl
NHCOCH3
CH3O
CO2H
CH2=CHCH2 CH
CO2H
Ph3P=CHCHO
N
O2N N CH3
CH2CH2OH
CH3
CH3 NN
COCH2CN
CH3
Br NO2
COCH3
Br
OH
NH2 .HCl
B22324 trans-2-Aminocyclohexanol hydrochloride, 99%
CAS: 5456-63-3
A14079 Tetronic acid, 96%
CAS: 541-57-1
L02161 Hexaethylene glycol, 96%
CAS: 2615-15-8
H33367 trans-2-Ethoxyethenyl-1-boronic acid pinacol
ester, 98% CAS: 1201905-61-4
CN CH2=CH(CH2)3Br
HO
O O
CH3
S
CO2H
CCl3
C
NH
OC(CH3)3
H(OCH2CH2)6OH
CH2CH2OH
(CH3)3COOCCH=PPH3
CH3
CH3
CH3
CH3
O
O
B
O
CH3
CN CH2=CH(CH2)3Br
HO
O O
CH3
S
CO2H
CCl3
C
NH
OC(CH3)3
H(OCH2CH2)6OH
CH2CH2OH
(CH3)3COOCCH=PPH3
CH3
CH3
CH3
CH3
O
O
B
O
CH3
CN CH2=CH(CH2)3Br
HO
O O
CH3
S
CO2H
CCl3
C
NH
OC(CH3)3
H(OCH2CH2)6OH
CH2CH2OH
(CH3)3COOCCH=PPH3
CH3
CH3
CH3
CH3
O
O
B
O
CH3
CN CH2=CH(CH2)3Br
HO
O O
CH3
S
CO2H
CCl3
C
NH
OC(CH3)3
H(OCH2CH2)6OH
CH2CH2OH
(CH3)3COOCCH=PPH3
CH3
CH3
CH3
CH3
O
O
B
O
CH3
CN CH2=CH(CH2)3Br
HO
O O
CH3
S
CO2H
CCl3
C
NH
OC(CH3)3
H(OCH2CH2)6OH
CH2CH2OH
(CH3)3COOCCH=PPH3
CH3
CH3
CH3
CH3
O
O
B
O
CH3
CN CH2=CH(CH2)3Br
HO
O O
CH3
S
CO2H
CCl3
C
NH
OC(CH3)3
H(OCH2CH2)6OH
CH2CH2OH
(CH3)3COOCCH=PPH3
CH3
CH3
CH3
CH3
O
O
B
O
CH3
High Purity Inorganics and Salts
Find out more at alfa.com
For Research Use Only. Not for use in diagnostic procedures. © 2019 Thermo Fisher Scientific Inc. All rights reserved. All trademarks are the property of Thermo Fisher Scientific and its subsidiaries unless otherwise specified.
CH3
CH3
COO Zn 2+
2
MnSO4.4H2O Fe
Pd(NO3)2.xH2O Ag2CO3 PbI2
CsOH.xH2O ZrCl4 AgBF4
CH3
CH3
COO Zn 2+
2
MnSO4.4H2O Fe
Pd(NO3)2.xH2O Ag2CO3 PbI2
CsOH.xH2O ZrCl4 AgBF4
CH3
CH3
COO Zn 2+
2
MnSO4.4H2O Fe
Pd(NO3)2.xH2O Ag2CO3 PbI2
CsOH.xH2O ZrCl4 AgBF4
039560 Zinc 2-ethylhexanoate
CAS: 136-53-8
011035 Palladium(II) nitrate hydrate, 99.8%
(metals basis), Pd 39% min CAS: 10102-05-3
013233 Cesium hydroxide hydrate, 99.9%
(metals basis) CAS: 12260-45-6
CH3
CH3
COO Zn 2+
2
MnSO4.4H2O Fe
Pd(NO3)2.xH2O Ag2CO3 PbI2
CsOH.xH2O ZrCl4 AgBF4
CH3
CH3
COO Zn 2+
2
MnSO4.4H2O Fe
Pd(NO3)2.xH2O Ag2CO3 PbI2
CsOH.xH2O ZrCl4 AgBF4
CH3
CH3
COO Zn 2+
2
MnSO4.4H2O Fe
Pd(NO3)2.xH2O Ag2CO3 PbI2
CsOH.xH2O ZrCl4 AgBF4
B22081 Manganese(II) sulfate tetra- hydrate,
99% (metals basis) CAS: 10101-68-5
011420 Silver carbonate, 99.5% (metals basis)
CAS: 534-16-7
012104 Zirconium(IV) chloride, Reactor Grade,
99.5+% (metals basis) CAS: 10026-11-6
010621 Iron powder, -22 mesh, Puratronic®,
99.998% (metals basis) CAS: 7439-89-6
044314 Lead(II) iodide, ultra dry, 99.999%
(metals basis) CAS: 10101-63-0
011539 Silver tetrafluoroborate, 99%
CAS: 14104-20-2
CH3
CH3
COO Zn 2+
2
MnSO4.4H2O Fe
Pd(NO3)2.xH2O Ag2CO3 PbI2
CsOH.xH2O ZrCl4 AgBF4
CH3
CH3
COO Zn 2+
2
MnSO4.4H2O Fe
Pd(NO3)2.xH2O Ag2CO3 PbI2
CsOH.xH2O ZrCl4 AgBF4
CH3
CH3
COO Zn 2+
2
MnSO4.4H2O Fe
Pd(NO3)2.xH2O Ag2CO3 PbI2
CsOH.xH2O ZrCl4 AgBF4