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3-Pyridinecarbonitrile, 4-(4-chlorophenyl)-1,6-dihydro-6-oxo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

825638-08-2

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825638-08-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 825638-08-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,5,6,3 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 825638-08:
(8*8)+(7*2)+(6*5)+(5*6)+(4*3)+(3*8)+(2*0)+(1*8)=182
182 % 10 = 2
So 825638-08-2 is a valid CAS Registry Number.

825638-08-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-chlorophenyl)-6-oxo-1H-pyridine-3-carbonitrile

1.2 Other means of identification

Product number -
Other names 3-Pyridinecarbonitrile,4-(4-chlorophenyl)-1,6-dihydro-6-oxo

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:825638-08-2 SDS

825638-08-2Downstream Products

825638-08-2Relevant academic research and scientific papers

Process for preparation of pyridine derivatives

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Page/Page column 8, (2010/02/10)

The present invention relates to a process for the manufacture of compounds of formula wherein the substituents are as described herein which comprises the steps of a) reacting a compound of formula with a compound of formula to form a compound of formula b) converting the OH/═O function of compounds of formula XIV/XIVa into a leaving group P with a reagent containing a leaving group, selected from POCl3, PBr3, MeI and (F3CSO2)2O to form a compound of formula wherein P is halogen or trifluoromethanesulfonate; c) substituting R2 for the leaving group P by reacting compound XV with HR2 to form a compound of formula and d) hydrolyzing the nitrile function in an acidic medium selected from H2SO4, HCl and acetic acid, to form a compound of formula I The compounds of formula I are valuable intermediates for the manufacture of therapeutically active compounds which have NK-1 antagonist activity.

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