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113729-10-5

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113729-10-5 Usage

General Description

1-Azabicyclo[3.1.0]hexane-5-carboxylicacid, methylester (9CI) is a chemical compound with a molecular formula C8H13NO2. It belongs to the azabicyclo compounds and is commonly used in pharmacological research. 1-Azabicyclo[3.1.0]hexane-5-carboxylicacid,methylester(9CI) has a bicyclic structure with a nitrogen atom in the ring, giving it unique chemical and biological properties. It is known for its potential activity as a neurotransmitter receptor modulator and has been studied for its potential therapeutic effects in various neurological and psychiatric disorders. Additionally, it has been investigated for its potential antiparasitic and antiviral properties. The methylester form of this compound is commonly used in the synthesis of other pharmaceutical compounds, making it an important intermediate in the production of various drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 113729-10-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,7,2 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 113729-10:
(8*1)+(7*1)+(6*3)+(5*7)+(4*2)+(3*9)+(2*1)+(1*0)=105
105 % 10 = 5
So 113729-10-5 is a valid CAS Registry Number.

113729-10-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 5-azabicyclo[3.1.0]hexane-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1-azabicyclo<3.1.0>hexane-3-carboxylate de methyle

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:113729-10-5 SDS

113729-10-5Downstream Products

113729-10-5Relevant articles and documents

Formation of azomethine ylids by thermolysis of oxazolidines. Study of the reaction in solution and in the gaseous phase

Bureau, R.,Mortier, J.,Joucla, M.

, p. 584 - 596 (2007/10/02)

Thermolysis of oxazolidines leads to azomethine ylids via cycloreversion.In the liquid phase, these intermediates then give 1-3 dipolar cycloaddition; in the gaseous phase, they lead to aziridines.With an alkyl group in position 2, we observed also the formation of enamines.The effect of substituents on both the cycloreversion reaction and the evolution of azomethine ylids was studied.The mechanism of the process tautomerism aziridine -> azomethine ylid -> enamine is discussed.Keywords - azomethine ylids / oxazolidines / cycloreversion / aziridines / enamines / tautomerism

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