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Methyl indolizine-7-carboxylate is a chemical compound derived from the bicyclic aromatic indolizine, serving as a methyl ester of indolizine-7-carboxylic acid. It is recognized for its potential as a precursor in the synthesis of various indolizine-based compounds, particularly in the pharmaceutical industry for the development of new drug molecules and in organic chemistry as a building block for heterocyclic compounds. Its unique structure and reactivity are valuable for researchers and chemists in the creation of new chemical entities and materials.

887602-89-3

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887602-89-3 Usage

Uses

Used in Pharmaceutical Industry:
Methyl indolizine-7-carboxylate is used as a precursor in the synthesis of new drug molecules, leveraging its unique structure to contribute to the development of innovative pharmaceutical compounds.
Used in Organic Chemistry:
In the field of organic chemistry, methyl indolizine-7-carboxylate is utilized as a building block for the synthesis of heterocyclic compounds, providing a foundation for the creation of complex organic molecules with diverse applications.

Check Digit Verification of cas no

The CAS Registry Mumber 887602-89-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,7,6,0 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 887602-89:
(8*8)+(7*8)+(6*7)+(5*6)+(4*0)+(3*2)+(2*8)+(1*9)=223
223 % 10 = 3
So 887602-89-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H9NO2/c1-13-10(12)8-4-6-11-5-2-3-9(11)7-8/h2-7H,1H3

887602-89-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl indolizine-7-carboxylate

1.2 Other means of identification

Product number -
Other names methyl indolizine-7-carboxylate

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 -
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More Details:887602-89-3 SDS

887602-89-3Downstream Products

887602-89-3Relevant academic research and scientific papers

Phosphines catalyzed nucleophilic addition of azoles to allenes: Synthesis of allylazoles and indolizines

Virieux, David,Guillouzic, Anne-Fran?oise,Cristau, Henri-Jean

, p. 3710 - 3720 (2006)

Triphenylphosphine was used as nucleophilic catalyst for umpolung addition of azoles to electron-deficient allenes. This strategy offers a simple and efficient method for functional allylation of azoles under neutral conditions and affords heterocyclic substituted Michael olefins. Furthermore, this catalytic methodology has been extended to addition-cyclization reactions between electron-deficient allenes or alkynes and pyrrole-2-carboxaldehyde in the presence of catalytic amount of tributylphosphine. In such conditions, substituted indolizine-7-carboxylates are easily obtained.

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