764183

APhos Pd G3

97%

Manufacturer: Sigma Aldrich

CAS Number: 1820817-64-8

Synonym(S): APhos-Pd-G3, Palladium G3-(4-(N,N-Dimethylamino)phenyl)di-tert-butylphosphine, [4-(Di-tert-butylphosphino)-N,N-dimethylaniline-2-(2′-aminobiphenyl)]palladium(II) methanesulfonate

Select a Size

Pack Size SKU Availability Price
5 G 764183-5-G In Stock ₹ 751.47
250 MG 764183-250-MG In Stock ₹ 7,958.70
IND870-1G 764183-IND870-1G In Stock ₹ 12,330.00
1 G 764183-1-G In Stock ₹ 24,686.40
IND870-5G 764183-IND870-5G In Stock ₹ 46,510.00

764183 - 5 G

₹ 751.47

In Stock

Quantity

1

Base Price: ₹ 751.47

GST (18%): ₹ 135.265

Total Price: ₹ 886.735

Quality Level

100

Assay

97%

form

solid

feature

generation 3

reaction suitability

core: palladiumreaction type: Buchwald-Hartwig Cross Coupling Reactionreaction type: Heck Reactionreaction type: Hiyama Couplingreaction type: Negishi Couplingreaction type: Sonogashira Couplingreaction type: Stille Couplingreaction type: Suzuki-Miyaura Couplingreagent type: catalystreaction type: Cross Couplings

mp

192-201 °C (decomposition)

functional group

phosphine

SMILES string

NC1=C(C=CC=C1)C2=C([Pd]OS(C)(=O)=O)C=CC=C2.CN(C)C3=CC=C(C=C3)P(C(C)(C)C)C(C)(C)C

InChI

1S/C16H28NP.C12H10N.CH4O3S.Pd/c1-15(2,3)18(16(4,5)6)14-11-9-13(10-12-14)17(7)8;13-12-9-5-4-8-11(12)10-6-2-1-3-7-10;1-5(2,3)4;/h9-12H,1-8H3;1-6,8-9H,13H2;1H3,(H,2,3,4);/q;;;+1/p-1

InChI key

SNUBBUQVCDWEAV-UHFFFAOYSA-M

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Description

  • Application: APhos Pd G3 is a Buchwald precatalyst that can be used in cross-coupling reactions.[1][2]

SAFETY INFORMATION

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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764183

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Quality Level:
100

Assay:
97%

form:
solid

feature:
generation 3

reaction suitability:
core: palladiumreaction type: Buchwald-Hartwig Cross Coupling Reactionreaction type: Heck Reactionreaction type: Hiyama Couplingreaction type: Negishi Couplingreaction type: Sonogashira Couplingreaction type: Stille Couplingreaction type: Suzuki-Miyaura Couplingreagent type: catalystreaction type: Cross Couplings

mp:
192-201 °C (decomposition)

functional group:
phosphine

SMILES string:
NC1=C(C=CC=C1)C2=C([Pd]OS(C)(=O)=O)C=CC=C2.CN(C)C3=CC=C(C=C3)P(C(C)(C)C)C(C)(C)C

InChI:
1S/C16H28NP.C12H10N.CH4O3S.Pd/c1-15(2,3)18(16(4,5)6)14-11-9-13(10-12-14)17(7)8;13-12-9-5-4-8-11(12)10-6-2-1-3-7-10;1-5(2,3)4;/h9-12H,1-8H3;1-6,8-9H,13H2;1H3,(H,2,3,4);/q;;;+1/p-1

InChI key:
SNUBBUQVCDWEAV-UHFFFAOYSA-M

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mp:
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functional group:
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SMILES string:
C#CCOCCOCCOCCOCCOCCC(ON1C(CCC1=O)=O)=O

InChI:
1S/C18H27NO9/c1-2-6-23-8-10-25-12-14-27-15-13-26-11-9-24-7-5-18(22)28-19-16(20)3-4-17(19)21/h1H,3-15H2

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ACZDUKRWTPZVRP-UHFFFAOYSA-N

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mp:
62-67 °C

functional group:
alkynemaleimide

SMILES string:
O=C(N1CCC(NCCOCCOCCOCCOCC#C)=O)C=CC1=O

InChI:
1S/C18H26N2O7/c1-2-8-24-10-12-26-14-15-27-13-11-25-9-6-19-16(21)5-7-20-17(22)3-4-18(20)23/h1,3-4H,5-15H2,(H,19,21)

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GHEBECZRHJXPTL-UHFFFAOYSA-N

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mp:
55-64 °C

functional group:
__

SMILES string:
O=C(NCCOCCOCCOCCOCC#C)CCCC[C@@H](SC1)[C@@]2([H])[C@]1([H])NC(N2)=O

InChI:
1S/C21H35N3O6S/c1-2-8-27-10-12-29-14-15-30-13-11-28-9-7-22-19(25)6-4-3-5-18-20-17(16-31-18)23-21(26)24-20/h1,17-18,20H,3-16H2,(H,22,25)(H2,23,24,26)/t17-,18-,20-/m1/s1

InChI key:
SKMJWNZZFUDLKQ-QWFCFKBJSA-N