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152438-62-5

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152438-62-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 152438-62-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,4,3 and 8 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 152438-62:
(8*1)+(7*5)+(6*2)+(5*4)+(4*3)+(3*8)+(2*6)+(1*2)=125
125 % 10 = 5
So 152438-62-5 is a valid CAS Registry Number.

152438-62-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methyl-2-propanyl {(2S)-1-[4-(benzyloxy)phenyl]-4-chloro-3-oxo- 2-butanyl}carbamate

1.2 Other means of identification

Product number -
Other names Boc-L-a-phenylglycine

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:152438-62-5 SDS

152438-62-5Relevant articles and documents

Synthesis and pharmacokinetic profile of highly deuterated brecanavir analogs

Velthuisen, Emile J.,Baughman, Todd M.,Johns, Brian A.,Temelkoff, David P.,Weatherhead, Jason G.

, p. 202 - 212 (2013/07/27)

Several highly deuterated analogs of the HIV-1 protease inhibitor brecanavir have been prepared to study the effect of deuterium upon metabolic stability. The sites for deuterium incorporation were initially chosen to maximize the potential for a kinetic isotope effect; locations where C-H bond breaking is the rate limiting step. The analogs have been profiled in both in vitro and in vivo pharmacokinetic studies and the result will be described herein.

PROCESS FOR PRODUCING AMINOEPOXIDE

-

Page 9, (2010/02/10)

The present invention relates to a method of producing N-carbamate protected-3-amino-1,2-epoxy-4-(hydroxy substituted phenyl)butane at a high optical purity in a high yield, by hydrogenating N-carbamate protected-3-amino-1-chloro-2-hydroxy-4-(benzyloxy su

A practical method for the preparation of α'-chloroketones of N-carbanaate protected-α-aminoacids

Chen, Ping,Cheng, Peter T. W.,Spergel, Steven H.,Zahler, Robert,Wang, Xuebao,Thottathil, John,Barrish, Joel C.,Polniaszek, Richard P.

, p. 3175 - 3178 (2007/10/03)

A practical method for the preparation of α-N-BOC-epoxides from protected amino acid esters based on the Kowalski homologation reaction is described. This procedure can be readily performed on a large scale without the use of hazardous reagents and has allowed preparation of epoxides 3 in multi-kilogram quantities.

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