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1H-Pyrrolo[2,3-b]pyridine, 3-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

161225-76-9

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161225-76-9 Usage

Type of compound

heterocyclic compound

Structure

pyrrolopyridine ring system with a phenylmethyl substituent at the 3-position

Use in industry

building block for the synthesis of biologically active compounds, potential drug candidates

Therapeutic applications

potential applications in oncology and neurology

Research use

development of new chemical processes and methodologies

Check Digit Verification of cas no

The CAS Registry Mumber 161225-76-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,2,2 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 161225-76:
(8*1)+(7*6)+(6*1)+(5*2)+(4*2)+(3*5)+(2*7)+(1*6)=109
109 % 10 = 9
So 161225-76-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H12N2/c1-2-5-11(6-3-1)9-12-10-16-14-13(12)7-4-8-15-14/h1-8,10H,9H2,(H,15,16)

161225-76-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-Pyrrolo[2,3-b]pyridine, 3-(phenylmethyl)-

1.2 Other means of identification

Product number -
Other names -

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:161225-76-9 SDS

161225-76-9Downstream Products

161225-76-9Relevant academic research and scientific papers

A convenient method for the preparation of 5-, 6- and 7-azaindoles and their derivatives

Hands, David,Bishop, Brian,Cameron, Mark,Edwards, John S.,Cottrell, Ian F.,Wright, Stanley H. B.

, p. 877 - 882 (1996)

The directed ortho lithiation of 2-tert-butoxycarbonylamino-3-methylpyridine (6a) has provided a convenient method for the preparation of 1H-pyrrolo[2,3-b]pyridine (4a, 7-azaindole). This procedure has been used to prepare a range of 3-substituted 2-tert-butoxycarbonylaminopyridines 6, 2- and 3-substituted and 2,3-disubstituted 1H-pyrrolo[2,3-b]pyridines 4 and shown to be of value in the preparation of 1H-pyrrolo[3,2-c]pyridine (15, 5-azaindole) and 1H-pyrrolo[2,3-c]pyridine (18, 6-azaindole) and derivatives.

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