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76800-88-9

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76800-88-9 Usage

General Description

1-(3,4-dimethoxyphenyl)-5-methoxy-2-methylcyclohepta[c]pyrrol-6(2H)-one is a chemical compound with a complex molecular structure. It contains a seven-membered cycloheptane ring fused to a pyrrole ring, with a methoxy group and a dimethoxyphenyl group attached to the cycloheptane ring. Additionally, there is a methoxy and a methyl group attached to the pyrrole ring. 1-(3,4-dimethoxyphenyl)-5-methoxy-2-methylcyclohepta[c]pyrrol-6(2H)-one has potential biological activity and may be used in pharmaceutical research and drug development due to its structural features. Its specific functional properties and potential applications would need to be further studied and determined.

Check Digit Verification of cas no

The CAS Registry Mumber 76800-88-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,8,0 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 76800-88:
(7*7)+(6*6)+(5*8)+(4*0)+(3*0)+(2*8)+(1*8)=149
149 % 10 = 9
So 76800-88-9 is a valid CAS Registry Number.

76800-88-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3,4-dimethoxyphenyl)-5-methoxy-2-methylcyclohepta[c]pyrrol-6-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:76800-88-9 SDS

76800-88-9Downstream Products

76800-88-9Relevant articles and documents

Rearrangement of Benzylaminonitriles to give Cycloheptapyrrol-6(2H)-ones

Waigh, Roger D.

, p. 1164 - 1165 (1980)

N-4-Methoxybenzyl- and N-3,4-dimethoxybenzyl-aminoacetonitriles with both 2-aryl and N-alkyl substituents undergo O-demethylation and rearrangement with elimination of ammonia in concentrated sulphuric acid to give 1-aryl-N-alkylcycloheptapyrrol-6(2H)-ones.

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