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145934-65-2

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145934-65-2 Usage

Structure

Pyrrolopyridine derivative with a bromine atom at the 5-position and two methyl groups at the 2 and 3 positions

Type

Organic compound

Usage

Building block in the synthesis of pharmaceuticals and agrochemicals

Pharmacological properties

Potential as an antiviral and antifungal agent

Electronic applications

Investigated for use in organic light-emitting diodes (OLEDs) and other electronic applications due to its electron transport properties

Check Digit Verification of cas no

The CAS Registry Mumber 145934-65-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,9,3 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 145934-65:
(8*1)+(7*4)+(6*5)+(5*9)+(4*3)+(3*4)+(2*6)+(1*5)=152
152 % 10 = 2
So 145934-65-2 is a valid CAS Registry Number.

145934-65-2SDS

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 5-Bromo-2,3-dimethyl-1H-pyrrolo[2,3-b]pyridine

1.2 Other means of identification

Product number -
Other names 1H-Pyrrolo[2,3-b]pyridine,5-bromo-2,3-dimethyl

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:145934-65-2 SDS

145934-65-2Relevant articles and documents

Preparation of 2,3-Disubstituted 5-Bromo-1 H -pyrrolo[2,3- b ]pyridine Framework by Fischer Cyclization

Alekseyev, Roman S.,Amirova, Sabina R.,Terenin, Vladimir I.

, p. 3169 - 3178 (2015/10/19)

A simple synthesis of some hard-to-reach heterocycles containing 2,3-disubstituted 5-bromo-1H-pyrrolo[2,3-b]pyridine framework by FisNher indole cyclization in polyphosphoric acid has been developed. A particularly valuable feature of this synthetic route is the possibility to build a 5-bromo-7-azaindole scaffold with alkyl or aryl substituents at positions 2 and 3 from available starting materials.

PYRAZOLE COMPOUNDS

-

Page/Page column 70-71, (2009/03/07)

The present invention is directed to compounds of Formula (I) and to pharmaceutically acceptable salts thereof, their synthesis, and their use as Raf inhibitors.

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