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936553-15-0

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936553-15-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 936553-15-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,6,5,5 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 936553-15:
(8*9)+(7*3)+(6*6)+(5*5)+(4*5)+(3*3)+(2*1)+(1*5)=190
190 % 10 = 0
So 936553-15-0 is a valid CAS Registry Number.

936553-15-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Piperazinecarboxylic acid, 2-(hydroxymethyl)-4-(phenylmethyl)-, 1,1-dimethylethyl ester

1.2 Other means of identification

Product number -
Other names TERT-BUTYL 4-BENZYL-2-(HYDROXYMETHYL)PIPERAZINE-1-CARBOXYLATE

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:936553-15-0 SDS

936553-15-0Relevant articles and documents

General Procedures for the Lithiation/Trapping of N-Boc Piperazines

Firth, James D.,O'Brien, Peter,Ferris, Leigh

, p. 7023 - 7031 (2017/07/17)

To provide α-substituted piperazines for early stage medicinal chemistry studies, a simple, general synthetic approach is required. Here, we report the development of two general and simple procedures for the racemic lithiation/trapping of N-Boc piperazin

Discovery of novel leukotriene A4 hydrolase inhibitors based on piperidine and piperazine scaffolds

Sandanayaka, Vincent,Mamat, Bjorn,Bhagat, Nikhil,Bedell, Louis,Halldorsdottir, Gudrun,Sigthorsdottir, Heida,Andrésson, Thorkell,Kiselyov, Alex,Gurney, Mark,Singh, Jasbir

scheme or table, p. 2851 - 2854 (2010/08/06)

Novel piperidine and piperazine derivatives have been designed and tested as inhibitors of LTA4 hydrolase (LTA4H). Most potent compounds showed good potency in both enzymatic and functional human whole blood assay. Crystallography studies further confirmed observed structure-activity relationship and LTA4H binding mode for analogs from the piperidine series.

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