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1-(2-chloro-pyridin-3-yl)-3-phenyl-urea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61964-07-6

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61964-07-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61964-07-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,9,6 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 61964-07:
(7*6)+(6*1)+(5*9)+(4*6)+(3*4)+(2*0)+(1*7)=136
136 % 10 = 6
So 61964-07-6 is a valid CAS Registry Number.

61964-07-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-chloropyridin-3-yl)-3-phenylurea

1.2 Other means of identification

Product number -
Other names 2-chloro-3-(3-phenylureido)pyridine

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:61964-07-6 SDS

61964-07-6Relevant academic research and scientific papers

Two-step synthesis of 3-aryl-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-ones

Scott, Jeremy P.

, p. 2083 - 2086 (2008/02/05)

One-pot tandem palladium-catalysed amination and intramolecular amidation of tert-butyl (2-chloropyridin-3-yl)carbamate with substituted primary anilines allows for the preparation of 3-arylated 1,3-dihydro-2H-imidazo[4,5-b]pyridin-2- ones (49-90% yield)

Imidazo pyridine-2-ones and pharmaceutical compositions and methods of treatment utilizing same

-

, (2008/06/13)

1,3-Dihydroimidazo[4,5-b]pyridin-2-ones and corresponding thiones have utility as analgesic, antipyretic and antiinflammatory agents. They are generally prepared by treatment of a 2,3-diaminopyridine with phosgene or thiosphosgene followed by further substitution if desired.

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