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6-(4-fluorophenoxy)pyridine-3-carbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

99902-74-6

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99902-74-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99902-74-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,9,0 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 99902-74:
(7*9)+(6*9)+(5*9)+(4*0)+(3*2)+(2*7)+(1*4)=186
186 % 10 = 6
So 99902-74-6 is a valid CAS Registry Number.

99902-74-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(4-fluorophenoxy)pyridine-3-carbonitrile

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:99902-74-6 SDS

99902-74-6Downstream Products

99902-74-6Relevant academic research and scientific papers

NOVEL THIOL DERIVATIVE, PROCESS FOR PRODUCING THE SAME AND USE THEREOF

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Page 38-39, (2010/02/10)

The present invention provides a novel thiol derivative [I] which has an excellent matrix metalloprotease inhibiting activity and is useful as a pharmaceutical composition, particularly a therapeutic agent or prophylactic agent for osteoarthritis and rheu

Antipicornavirus activity of substituted phenoxybenzenes and phenoxypyridines

Markley,Tong,Dulworth,Steward,Goralski,Johnston,Wood,Vinogradoff,Bargar

, p. 427 - 433 (2007/10/02)

Phenoxybenzenes and phenoxypyridines were prepared and tested for the effect of substituents on antipicornavirus activity. The most active compound, 2-(3,4-dichlorophenoxy)-5-nitrobenzonitrile (8), demonstrated broad-spectrum antipicornavirus activity. Co

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