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6,8-dimethylcyclopenta[4,5]azepino[2,1,7-cd]pyrrolizine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65738-45-6

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65738-45-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65738-45-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,7,3 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 65738-45:
(7*6)+(6*5)+(5*7)+(4*3)+(3*8)+(2*4)+(1*5)=156
156 % 10 = 6
So 65738-45-6 is a valid CAS Registry Number.

65738-45-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Cyclopent(4,5)azepino(2,1,7-cd)pyrrolizine, 6,8-dimethyl-

1.2 Other means of identification

Product number -
Other names 6,8-dimethylcyclopenta[4,5]azepino(7,1,2-cd)pyrrolizine

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:65738-45-6 SDS

65738-45-6Downstream Products

65738-45-6Relevant academic research and scientific papers

Heterocyclic Compounds with Bridgehead Nitrogen Atoms. Part 8. The Synthesis and Properties of Cyclopentaazepinopyrrolizine (Cyclopentacyclazine)

Jessep, Michael A.,Leaver, Derek

, p. 1324 - 1330 (1980)

The title compound is obtained (i) by the reaction of 5-(NN-dimethylaminomethylene)-1-(NN-dimethyliminiomethyl)cyclopenta-1,3-diene perchlorate with the conjugate base of 3H-pyrrolizine or (ii), in better yield, by the reaction of 3,5-bis-(NN-dimethylaminomethylene)-3H,5H-pyrrolizinium perchlorate with the conjugate base of cyclopentadiene.The compound resembles azulene in its visible and near-u.v. spectrum and in the ease of electrophilic attack in the five-membered carbocyclic ring (position 6 and 8).Products of acylation, nitration, nitrosation, bromination, and NN-dimethylaminomethylation are described.

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