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Merck
CN

481084

rac-BINAP

greener alternative

97%

别名:

(±)-2,2′-双(二苯基膦)-1,1′-联萘, 2,2′-双(二苯基膦)-1,1′-联萘, (±)-BINAP, [1,1′-联萘]-2,2′-双二苯膦

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关于此项目

线性分子式:
[(C6H5)2PC10H6-]2
化学文摘社编号:
分子量:
622.67
UNSPSC Code:
12352005
PubChem Substance ID:
NACRES:
NA.22
Beilstein/REAXYS Number:
5321443
MDL number:
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Quality Level

product line

Buchwald Ligand

assay

97%

reaction suitability

reaction type: Cross Couplings, reagent type: ligand
reaction type: Acylations, reagent type: ligand
reaction type: Arylations, reagent type: ligand
reaction type: Buchwald-Hartwig Cross Coupling Reaction, reagent type: ligand
reaction type: C-C Bond Formation, reagent type: ligand
reaction type: Decarboxylations, reagent type: ligand
reaction type: Stille Coupling

greener alternative product characteristics

Catalysis
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

mp

283-286 °C (lit.)

functional group

phosphine

greener alternative category

SMILES string

P(c8ccccc8)(c7ccccc7)c1c(c6c(cc1)cccc6)c2c3c(ccc2P(c5ccccc5)c4ccccc4)cccc3

InChI

1S/C44H32P2/c1-5-19-35(20-6-1)45(36-21-7-2-8-22-36)41-31-29-33-17-13-15-27-39(33)43(41)44-40-28-16-14-18-34(40)30-32-42(44)46(37-23-9-3-10-24-37)38-25-11-4-12-26-38/h1-32H

InChI key

MUALRAIOVNYAIW-UHFFFAOYSA-N

General description

外消旋型 BINAP。
We are committed to bringing you Greener Alternative Products, which adhere to one of the four categories of Greener Alternatives. This product falls under category 12 PAP and aligns with the Green Chemistry Principle of Catalysis. It is an outstanding chiral ligand for asymmetric hydrogenation catalysis, providing extremely high enantioselective recognition. Click here for more information.

Application

钯催化芳基胺偶联反应的配体,用于制备去甲基硫代秋水仙碱。可与 Cu(II) 联合使用催化芳基磺酰胺加成反应生成苯乙烯和烯烃。亦可用于钯催化的三联吡啶胺化反应。


存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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商品

Discover AdQPhos and its Pd pre-catalysts for selective α-arylation of diverse nucleophiles under mild aqueous conditions without hazardous solvents.

相关内容

Phosphine Ligand Application Guide


Advanced Synthesis & Catalysis, 345, 15-32 (2003)
Tetrahedron Letters, 47, 5079-5079 (2006)
Jason G Taylor et al.
Organic letters, 8(16), 3561-3564 (2006-07-28)
[reaction: see text] Regioselective additions of arylsulfonamides to vinylarenes, norbornene, and cyclohexadiene were achieved using a copper-diphosphine catayst under mild reaction conditions. These processes appear to be ligand-accelerated.



全球贸易项目编号

货号GTIN
481084-25G04061832388519
481084-100G04061833553305
481084-500G04061833502709
481084-5G04061832388526