99902-70-2 Usage
General Description
6-(4-Chlorophenoxy)nicotinonitrile is a chemical compound with the molecular formula C12H7ClNO. It is primarily used as a building block in the synthesis of various pharmaceuticals and agrochemicals. The compound is a nitrile derivative of 4-chlorophenol and nicotinic acid, and its structure contains both a nitrile and a chlorophenyl functional group. Due to its significance as an intermediate in the production of various chemicals, it is essential for use in the pharmaceutical and agrochemical industries. Additionally, it is used in research and development as a starting material for the synthesis of new potential drug candidates.
Check Digit Verification of cas no
The CAS Registry Mumber 99902-70-2 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 0 respectively.
Calculate Digit Verification of CAS Registry Number 99902-70:
(7*9)+(6*9)+(5*9)+(4*0)+(3*2)+(2*7)+(1*0)=182
182 % 10 = 2
So 99902-70-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H7ClN2O/c13-10-2-4-11(5-3-10)16-12-6-1-9(7-14)8-15-12/h1-6,8H
99902-70-2Relevant articles and documents
Thieme Chemistry Journals Awardees - Where Are They Now? Rhodium-Catalyzed Synthesis of Unsymmetric Di(heteroaryl) Ethers Using Heteroaryl Exchange Reaction
Tanii, Saori,Arisawa, Mieko,Tougo, Takaya,Horiuchi, Kiyofumi,Yamaguchi, Masahiko
supporting information, p. 1601 - 1607 (2017/08/11)
Unsymmetric di(heteroaryl) ethers were synthesized by the rhodium-catalyzed heteroaryl exchange reaction of heteroaryl aryl ethers and heteroaryl esters at equilibrium. Diverse unsymmetric di(heteroaryl) ethers containing five- and six-membered heteroaren
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
