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936103

Sigma-Aldrich

tBuXPhos Pd G6 Br

greener alternative

Synonym(s):

tBuXphos OAC precatalyst Br

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About This Item

Empirical Formula (Hill Notation):
C42H55BrNO2PPd
Molecular Weight:
823.19
UNSPSC Code:
12161600
NACRES:
NA.21
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form

powder

Quality Level

greener alternative product characteristics

Catalysis
Learn more about the Principles of Green Chemistry.

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Greener Alternative Product

greener alternative category

SMILES string

Br[Pd-](C1=CC=C(NC(OC2=CC=CC=C2)=O)C=C1)[P+](C(C=CC=C3)=C3C(C(C(C)C)=CC(C(C)C)=C4)=C4C(C)C)(C(C)(C)C)C(C)(C)C

General description

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Green Chemistry. This product has been enhanced for catalytic efficiency. Click here for more information.

Application

tBuXPhos Pd G6 Br is an oxadative addition complex (OAC) of tBuXPhos for use in bioconjugation. The OAC can be used to arylate cysteine followed by subsequent protein-peptide cross-linking.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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An efficient, one-pot, synthesis of dithiocarbamates from the corresponding alcohols using Mitsunobu's reagent.
Chaturvedi D and Ray S.
Tetrahedron Letters, 47(8), 1307-1309 (2006)
Copolymerization of ethylene sulfide and carbon disulfide.
Soga K, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 14(3), 677-684 (1976)
Nanosized titania and zirconia as catalysts for hydrolysis of carbon disulfide.
Yue Y, et al.
Applied Catalysis. B, Environmental, 46(3), 561-572 (2003)
1, 3-Dithiolium carbenes from acetylenes and carbon disulfide.
Hartzler HD.
Journal of the American Chemical Society, 95(13), 4379-4387 (1973)
Xanthogenation of lignocarbohydrates by carbon disulfide.
Efanov MV and Pershina LA.
Chemistry of Natural Compounds, 38(1), 90-94 (2002)

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