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936782

Sigma-Aldrich

P(o-tol)3 Pd G2 ChemBeads

同義詞:

Chloro[tri(o-tolyl)phosphine][2-(2′-amino-1,1′-biphenyl)]palladium(II), P(o tol) Pd G2

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About This Item

經驗公式(希爾表示法):
C33H31ClNPPd
CAS號碼:
分子量::
614.45
MDL號碼:
分類程式碼代碼:
31191513
NACRES:
NA.22

形狀

solid

品質等級

成份

, ~5 wt. % (loading of catalyst)

反應適用性

reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Cross Couplings
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
reagent type: catalyst

SMILES 字串

CC1=CC=CC=C1P(C2=CC=CC=C2C)C3=CC=CC=C3C.NC4=C(C5=C([Pd]Cl)C=CC=C5)C=CC=C4

InChI

InChI:1S/C21H21P.C12H10N.ClH.Pd/c1-16-10-4-7-13-19(16)22(20-14-8-5-11-17(20)2)21-15-9-6-12-18(21)3;13-12-9-5-4-8-11(12)10-6-2-1-3-7-10;;/h4-15H,1-3H3;1-6,8-9H,13H2;1H;/q;;;+1/p-1

InChI 密鑰

MNKLPYUHUVVRNW-UHFFFAOYSA-M

相關類別

一般說明

P(o-Tol)3 Pd G2 is an air stable, bulky electron-rich dialkylbiaryl phospine-based catalyst used in Pd-catalyzed cross - coupling reactions.

應用

ChemBeads are chemical coated glass beads. ChemBeads offer improved flowability and chemical uniformity perfect for automated solid dispensing and high-throughput experimentation. The method of creating ChemBeads uses no other chemicals or surfactants allowing the user to accurately dispense sub-milligram amounts of chemical.

For larger scale uses, product also available in powdered form (759163)

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3


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Noah P Tu et al.
Angewandte Chemie (International ed. in English), 58(24), 7987-7991 (2019-03-21)
Technologies that enable rapid screening of diverse reaction conditions are of critical importance to methodology development and reaction optimization, especially when molecules of high complexity and scarcity are involved. The lack of a general solid dispensing method for chemical reagents
Ana L Aguirre et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 27(51), 12981-12986 (2021-07-08)
High-throughput experimentation (HTE) methods are central to modern medicinal chemistry. While many HTE approaches to C-N and Csp2 -Csp2 bonds are available, options for Csp2 -Csp3 bonds are limited. We report here how the adaptation of nickel-catalyzed cross-electrophile coupling of

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