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139962-80-4

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139962-80-4 Usage

Type of compound

Heterocyclic compound

Core structure

Pyrrolopyrimidine

Substituent

Phenyl group

Attachment position

6th position

Pharmacological properties

Potential pharmacological properties

Use

Building block in the synthesis of various pharmaceuticals and biologically active molecules

Unique features

Unique structure and reactivity

Applications in medicinal chemistry

Development of novel drugs and therapeutic agents

Potential activities

Antitumor and antiviral activities

Interest for further study

Drug discovery and development.

Check Digit Verification of cas no

The CAS Registry Mumber 139962-80-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,9,6 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 139962-80:
(8*1)+(7*3)+(6*9)+(5*9)+(4*6)+(3*2)+(2*8)+(1*0)=174
174 % 10 = 4
So 139962-80-4 is a valid CAS Registry Number.

139962-80-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Phenyl<1H>pyrrolo<2,3-d>pyrimidine

1.2 Other means of identification

Product number -
Other names 6-phenyl-7H-pyrrolo[2,3-d]pyrimidine

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:139962-80-4 SDS

139962-80-4Downstream Products

139962-80-4Relevant articles and documents

One-pot synthesis of azaindoles via palladium-catalyzed α-heteroarylation of ketone enolates

Spergel, Steven H.,Okoro, Danielle R.,Pitts, William

supporting information; experimental part, p. 5316 - 5319 (2010/10/19)

(Figure presented) A convenient, one-pot method for the construction of a variety of azaindoles using simple ketones and haloaminopyridines is described.

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