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2-Azabicyclo[3.2.0]hepta-2,6-dien-3-amine(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24686-32-6

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24686-32-6 Usage

Structure

Bicyclic amine derivative with a three-carbon bridge and a six-membered ring

Complexity

Possesses a complex and unique molecular structure

Interest

Attracts attention for pharmaceutical and organic chemistry research

Properties

Specific properties are under continuous study and exploration by scientists

Applications

Potential applications in various fields, including pharmaceuticals and organic chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 24686-32-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,6,8 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 24686-32:
(7*2)+(6*4)+(5*6)+(4*8)+(3*6)+(2*3)+(1*2)=126
126 % 10 = 6
So 24686-32-6 is a valid CAS Registry Number.

24686-32-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-azabicyclo[3.2.0]hepta-3,6-dien-3-amine

1.2 Other means of identification

Product number -
Other names 2-aza-bicyclo[3.2.0]hepta-2,6-dien-3-ylamine

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:24686-32-6 SDS

24686-32-6Upstream product

24686-32-6Downstream Products

24686-32-6Relevant academic research and scientific papers

Photoisomerization of 3H-Azepines

Odum, Robert A.,Schmall, Bernard

, p. 1850 - 1869 (2007/10/03)

The photochemistry of 3H-azepines substituted in the 2-position with ethoxy, amino, and diethylamino-groups was investigated.The only major volatile products were the 3-substituted 2-azabicyclohepta-2,6-dienes, in all cases.One possible factor for the selective nature of the ring closure might be the preservation of amidine or imidine ester resonance energy.An unexpected transformation of an amidine to an imidate ester was found.

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