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163959-79-3

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163959-79-3 Usage

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Efficient ruthenium catalyst for asymmetric hydrogenation of aryl ketones.

Check Digit Verification of cas no

The CAS Registry Mumber 163959-79-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,3,9,5 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 163959-79:
(8*1)+(7*6)+(6*3)+(5*9)+(4*5)+(3*9)+(2*7)+(1*9)=183
183 % 10 = 3
So 163959-79-3 is a valid CAS Registry Number.

163959-79-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-Benzimidazole-2-methanamine,α-methyl-,(R)-(9CI)

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:163959-79-3 SDS

163959-79-3Relevant articles and documents

PF74 and its novel derivatives stabilize hexameric lattice of HIV-1 mature-like particles

?kach, Kry?tof,Dostálková, Al?běta,Flegel, Martin,Hadravová, Romana,Hrabal, Richard,K?í?ová, Ivana,Kaufman, Filip,Ruml, Tomá?,Rumlová, Michaela

, (2020/04/27)

A major structural retroviral protein, capsid protein (CA), is able to oligomerize into two different hexameric lattices, which makes this protein a key component for both the early and late stages of HIV-1 replication. During the late stage, the CA prote

Asymmetric Hydrogenation of 3,5-Bistrifluoromethyl Acetophenone in Pilot Scale with Industrially Viable Ru/Diphosphine-Benzimidazole Complexes

Xu, Liang,Huang, Zhi-Hong,Sandoval, Christian A.,Gu, Lian-Quan,Huang, Zhi-Shu

, p. 1137 - 1141 (2015/04/22)

A novel efficient asymmetric hydrogenation (AH) process was developed for the preparation of (R)-1-(3,5-bis(trifluoromethyl)phenyl)ethanol (3), using a catalyst Ru/(4R,5R)-(+)-4,5-bis(diphenylphosphinomethyl)-2,2-dimethyl-1,3-dioxoane-(R,R-Diop)-2R-(α-met

Hybrid NH2-benzimidazole ligands for efficient Ru-catalyzed asymmetric hydrogenation of aryl ketones

Li, Yuehui,Ding, Kuiling,Sandoval, Christian A.

supporting information; experimental part, p. 907 - 910 (2009/07/25)

Readily available hybrid NH2/benzimidazole ligands (R-bimaH, 1) dramatically influence the outcome of established Ru-based catalysts during asymmetric hydrogenation of aryl ketones. The benzimidazole functionality results in reversal of the typically observed chiral induction and allows for hydrogenation to be uncharacteristically conducted in nonprotic solvents. The developed systems efficiently catalyzed the AH of a number of ketones in up to 99% ee.

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