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162307-09-7

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162307-09-7 Usage

General Description

2-Acetyl-2-azabicyclo[2.2.1]hept-5-en-3-one is a chemical compound that is also known as tropanone. It is a bicyclic organic compound that contains a five-membered ring and a seven-membered ring. Tropanone is commonly used as an intermediate in the synthesis of various pharmaceutical compounds, including atropine and other tropane alkaloids. It is also used as a building block in the production of complex organic molecules. Tropanone has a variety of chemical and biological properties, and its structural features make it a useful starting material for the preparation of a wide range of different chemical compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 162307-09-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,3,0 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 162307-09:
(8*1)+(7*6)+(6*2)+(5*3)+(4*0)+(3*7)+(2*0)+(1*9)=107
107 % 10 = 7
So 162307-09-7 is a valid CAS Registry Number.

162307-09-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ACETYL-2-AZABICYCLO[2.2.1]HEPT-5-EN-3-ONE

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:162307-09-7 SDS

162307-09-7Relevant articles and documents

A practical enzymatic procedure for the resolution of N-substituted 2- azabicyclo[2.2.1]hept-5-en-3-one

Mahmoudian, Mahmoud,Lowdon, Andrew,Jones, Martin,Dawson, Michael,Wallis, Christopher

, p. 1201 - 1206 (1999)

A simple and efficient process for the enantioselective resolution of N- substituted 2-azabicyclo[2.2.1]hept-5-en-3-one has been developed using commercially available hydrolytic enzymes. This offers a practical approach for the preparation of enantiomerically pure N-substituted γ-lactams.

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