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5012-77-1

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5012-77-1 Usage

Heterocyclic compound

Consists of a seven-membered azepane ring and a methoxy-substituted pyridine ring

Use in organic chemistry and pharmaceutical research

Serves as a building block for the synthesis of various organic compounds and potential drug candidates

Structure and functional groups

Make it suitable for the development of new molecules with potential biological activity and therapeutic applications

Interest to researchers and scientists

Working in drug discovery and medicinal chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 5012-77-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,1 and 2 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5012-77:
(6*5)+(5*0)+(4*1)+(3*2)+(2*7)+(1*7)=61
61 % 10 = 1
So 5012-77-1 is a valid CAS Registry Number.

5012-77-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(6-methoxypyridin-2-yl)azepane

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:5012-77-1 SDS

5012-77-1Downstream Products

5012-77-1Relevant articles and documents

Superbase catalysis of oxazolidin-2-one ring formation from carbon dioxide and prop-2-yn-1-amines under homogeneous or heterogenous conditions

Costa, Mirco,Chiusoli, Gian Paolo,Taffurelli, Davide,Dalmonego, Giulio

, p. 1541 - 1546 (1998)

N-alkyl-substituted prop-2-yn-1-amines and N-tri-, tetra- and penta-alkyl-substituted guanidines or other strong organic bases assemble under the action of carbon dioxide to afford carbamates, from which methyleneoxazolidinones 2 are formed by ring closure. If alkyl or cycloalkyl chains of appropriate length are present in the guanidines the reaction readily occurs under heterogenous conditions without solvent.

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