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METHYL 2,3-DIHYDRO-1-INDOLECARBOXYLATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89875-37-6

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89875-37-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89875-37-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,8,7 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 89875-37:
(7*8)+(6*9)+(5*8)+(4*7)+(3*5)+(2*3)+(1*7)=206
206 % 10 = 6
So 89875-37-6 is a valid CAS Registry Number.

89875-37-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2,3-dihydroindole-1-carboxylate

1.2 Other means of identification

Product number -
Other names METHYL 2,3-DIHYDRO-1-INDOLECARBOXYLATE

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:89875-37-6 SDS

89875-37-6Relevant academic research and scientific papers

5-Membered N-heterocyclic compounds by dimethyl carbonate chemistry

Arico, Fabio,Toniolo, Umberto,Tundo, Pietro

experimental part, p. 58 - 61 (2012/03/26)

Aliphatic and aromatic 1,4-bifunctional compounds bearing a primary alcoholic function and an amine can be efficiently cyclised with dimethyl carbonates in the presence of a base to achieve 5-membered N-heterocyclic compounds. This novel synthetic pathway

Palladium-catalyzed sp3 C-H activation of simple alkyl groups: Direct preparation of indoline derivatives from N-alkyl-2-bromoanilines

Watanabe, Toshiaki,Oishi, Shinya,Fujii, Nobutaka,Ohno, Hiroaki

supporting information; experimental part, p. 1759 - 1762 (2009/04/12)

The sp3 C-H activation of a simple alkyl group catalyzed by palladium(O) provides a novel and convenient strategy for the synthesis of various indolines from simple precursors, such as N-alkyl-2-bromoanilines. This study demonstrates that assisting moieties In the substrate such as a pyridine or quaternary carbon are not always necessary for sp3 C-H activation.

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