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145618-11-7

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145618-11-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 145618-11-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,6,1 and 8 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 145618-11:
(8*1)+(7*4)+(6*5)+(5*6)+(4*1)+(3*8)+(2*1)+(1*1)=127
127 % 10 = 7
So 145618-11-7 is a valid CAS Registry Number.

145618-11-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl (2S)-2-amino-2-cyclohexylacetate

1.2 Other means of identification

Product number -
Other names CYC123

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:145618-11-7 SDS

145618-11-7Relevant articles and documents

Optimization of dipeptidic inhibitors of cathepsin L for improved Toxoplasma gondii selectivity and CNS permeability

Zwicker, Jeffery D.,Diaz, Nicolas A.,Guerra, Alfredo J.,Kirchhoff, Paul D.,Wen, Bo,Sun, Duxin,Carruthers, Vern B.,Larsen, Scott D.

supporting information, p. 1972 - 1980 (2018/04/14)

The neurotropic protozoan Toxoplasma gondii is the second leading cause of death due to foodborne illness in the US, and has been designated as one of five neglected parasitic infections by the Center for Disease Control and Prevention. Currently, no trea

Organocatalytic synthesis of optically active β-branched α-amino esters via asymmetric biomimetic transamination

Su, Cunxiang,Xie, Ying,Pan, Hongjie,Liu, Mao,Tian, Hua,Shi, Yian

, p. 5856 - 5860 (2014/08/05)

This paper describes an efficient asymmetric biomimetic transamination of α-keto esters with a quinine-derived chiral base as the catalyst, giving a variety of β-branched α-amino esters in 50-96% yield and 87-95% ee. This journal is the Partner Organisations 2014.

Rhodium/graphite-catalyzed hydrogenation of carbocyclic and heterocyclic aromatic compounds

Falini, Giuseppe,Gualandi, Andrea,Savoia, Diego

experimental part, p. 2440 - 2446 (2010/02/27)

Rhodium on graphite (Rh/Gr, C24Rh) was prepared by reaction of anhydrous rhodium trichloride with potassium graphite (C8K, 3 equivalents) and used as a heterogeneous catalyst for the hydrogenation of carbocyclic and heterocyclic aromatic compounds at room temperature and 1 atm of hydrogen pressure. The effect of substitution on the benzene ring was examined in a variety of derivatives, including those with alkyl, hydroxy, alkoxy, aryloxy, carboxy, amino, nitro, acyl, chloro, or functionalized alkyl groups. Reduction of carbonyl functions of aromatic aldehydes and ketones occurred with complete or partial cleavage of the benzylic C-O bond; this cleavage also occurred in the hydrogenation of benzylic alcohols and esters. Georg Thieme Verlag Stuttgart.

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