Welcome to LookChem.com Sign In|Join Free

CAS

  • or

887602-89-3

Post Buying Request

887602-89-3 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

887602-89-3 Usage

General Description

Methyl indolizine-7-carboxylate is a chemical compound that is a derivative of indolizine, a bicyclic aromatic compound. It is a methyl ester of indolizine-7-carboxylic acid, which is commonly used as a precursor in the synthesis of various indolizine-based compounds. methyl indolizine-7-carboxylate has potential applications in the pharmaceutical industry, particularly in the development of new drug molecules. It is also used in the field of organic chemistry as a building block for the synthesis of heterocyclic compounds. Its unique structure and reactivity make it a valuable tool for researchers and chemists working in the development of new chemical entities and materials.

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 -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:887602-89-3 SDS

887602-89-3Downstream Products

887602-89-3Relevant articles and documents

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.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 887602-89-3