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141395-84-8

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141395-84-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141395-84-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,3,9 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 141395-84:
(8*1)+(7*4)+(6*1)+(5*3)+(4*9)+(3*5)+(2*8)+(1*4)=128
128 % 10 = 8
So 141395-84-8 is a valid CAS Registry Number.

141395-84-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-(+)-N-(2,3-epoxypropyl)morpholine

1.2 Other means of identification

Product number -
Other names (S)-1,2-epoxy-3-morpholinopropane

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:141395-84-8 SDS

141395-84-8Relevant articles and documents

PYRROLO-NITROGENOUS HETEROCYCLIC DERIVATIVES, THE PREPARATION AND THE PHARMACEUTICAL USE THEREOF

-

Page/Page column 102-103, (2010/04/23)

The invention provides new pyrrolo-nitrogenous heterocyclic derivatives represented by formula (I) or their salts, the preparation thereof, pharmaceutical compositions containing such derivatives and the use of such derivatives as therapeutic agents, espe

Synthesis of the hypotensive agent 8-amino-7-[2-hydroxy-3-morpholinopropyl] theophylline (P23) and analogs

Cegla, Marek T.,Potaczek, Joanna,Zylewski, Marek,Strekowski, Lucjan

experimental part, p. 191 - 194 (2009/07/19)

Synthesis of a number of 7, 8-disubstituted theophyllines including enantiomers of the hypotensive agent P23 is described.

The synthesis of potent marcocyclic renin inhibitors

Dhanoa, Daljit S.,Parsons, William H.,Greenlee, William J.,Patchett, Arthur A.

, p. 1725 - 1728 (2007/10/02)

An efficient synthesis of a novel class of potent macrocylic renin inhibitors exemplified by compounds 1 and 2, which involves the marcocyclization of 8 and 9 as the key step, is described. The macrocyclic design of renin inhibitors 1 and 2 disclosed here

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