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126484-94-4

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126484-94-4 Usage

General Description

2-Azabicyclo[3.1.0]hexane-1-carboxylicacid,3-oxo-,methylester(9CI) is a chemical compound with the molecular formula C8H11NO3. It is a derivative of the bicyclic compound azabicyclohexane and is commonly used in the pharmaceutical industry as a building block for the synthesis of various drugs. This chemical compound is known for its potential use as an intermediate in organic synthesis and medicinal chemistry. Additionally, it is also utilized in research for its ability to interact with biological systems and potentially impact drug discovery and development. Overall, 2-Azabicyclo[3.1.0]hexane-1-carboxylicacid,3-oxo-,methylester(9CI) is a versatile compound with various potential applications in the field of pharmaceuticals and biological research.

Check Digit Verification of cas no

The CAS Registry Mumber 126484-94-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,4,8 and 4 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 126484-94:
(8*1)+(7*2)+(6*6)+(5*4)+(4*8)+(3*4)+(2*9)+(1*4)=144
144 % 10 = 4
So 126484-94-4 is a valid CAS Registry Number.

126484-94-4SDS

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 3-Oxo-2-aza-bicyclo[3.1.0]hexane-1-carboxylic acid methyl ester

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

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More Details:126484-94-4 SDS

126484-94-4Relevant articles and documents

THE SYNTHESIS AND CHARACTERIZATION OF 2,3-METHANOPYROGLUTAMIC ACID

Mapelli, Claudio,Elrod, Luther F.,Holt, Elizabeth M.,Stammer, Charles H.

, p. 4377 - 4382 (2007/10/02)

Details of the synthesis of 2,3-methanopyroglutamic acid (1), its N-methylamide (7) and N-β-naphthylamide (6) are reported.An NMR study of the conformation of 7 is discussed and the stability of the amide 6 to pyroglutamylaminopeptidase is detailed.The crystal structure of an alkene (4) formed during the pyrolysis of an intermediate pyrazoline (2) indicates that the (Z)-configuration is conserved during nitrogen extrusion.

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