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.
767-61-3Relevant academic research and scientific papers
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.
Low temperature organocopper-mediated two-component cross coupling/cycloisomerization approach toward N-fused heterocycles
Chernyak, Dmitri,Gadamsetty, Surendra Babu,Gevorgyan, Vladimir
supporting information; experimental part, p. 2307 - 2310 (2009/05/11)
(Chemical Equation Presented) Organocopper reagents smoothly react with heterocyclic propargyl mesylates at low temperature to produce N-fused heterocycles. The copper reagent plays a "double duty" in this novel cascade transformation, which proceeds via an SN2′ substitution followed by a subsequent cycloisomerization step.
