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767-61-3

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767-61-3 Usage

Heterocyclic compound

A compound containing a ring structure with both carbon and non-carbon atoms 1-Methylindolizine has a five-membered ring fused to a six-membered ring, with the non-carbon atom being nitrogen.

Indolizine derivative

A compound derived from the base structure of indolizine 1-Methylindolizine is classified as an indolizine derivative due to its similar structure and properties.

Biological activities

Exhibits various effects on biological systems 1-Methylindolizine has been found to have anti-inflammatory and antitumor properties.

Pharmaceutical applications

Potential use in the development of drugs 1-Methylindolizine has been studied for its potential pharmaceutical applications, mainly due to its biological activities.

Building block in organic synthesis

A starting compound used in the synthesis of more complex molecules 1-Methylindolizine has been investigated for its potential as a building block in organic synthesis, particularly in the development of new drugs and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 767-61-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,6 and 7 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 767-61:
(5*7)+(4*6)+(3*7)+(2*6)+(1*1)=93
93 % 10 = 3
So 767-61-3 is a valid CAS Registry Number.

767-61-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methylindolizine

1.2 Other means of identification

Product number -
Other names 1-Methylindolizin

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:767-61-3 SDS

767-61-3Relevant articles and documents

Organocopper-mediated two-component SN2’-substitution cascade towards N-fused heterocycles

Chernyak,Gevorgyan

, p. 1516 - 1526 (2018/01/26)

Organocuprates efficiently undergo reaction with heterocyclic propargyl mesylates at low temperature to produce N-fused heterocycles. The copper reagent plays a “double duty” in this cascade transformation, which proceeds through an SN2’-substitution followed by a consequent cycloisomerization step.

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