76574-43-1 Usage
General Description
2-(2,3-Dimethylphenyl)acetonitrile, also known as 2-(2,3-Xylidino)acetonitrile, is a chemical compound with the molecular formula C11H11N. It is a colorless to yellowish liquid that is used in various organic synthesis reactions and pharmaceutical applications. 2-(2,3-Dimethylphenyl)acetonitrile is derived from acetonitrile and 2,3-dimethylphenyl, and it can be used as an intermediate in the production of pharmaceuticals, agrochemicals, and other organic compounds. It is also used as a building block in the synthesis of various pharmacological agents and other organic molecules. 2-(2,3-Dimethylphenyl)acetonitrile has potential applications in the field of medicinal chemistry and drug discovery due to its structural versatility and synthetic utility.
Check Digit Verification of cas no
The CAS Registry Mumber 76574-43-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,5,7 and 4 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 76574-43:
(7*7)+(6*6)+(5*5)+(4*7)+(3*4)+(2*4)+(1*3)=161
161 % 10 = 1
So 76574-43-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H11N/c1-8-4-3-5-10(6-7-11)9(8)2/h3-5H,6H2,1-2H3
76574-43-1Relevant articles and documents
Process for the alkylation of alkyl-or benzylcyanogen derivatives in the presence of trialkylamines or trialkylphosphines
-
, (2008/06/13)
A process for the alkylation of compounds of the formula II where the reaction with the alkylating agent is carried out in the presence of a base and a trialkylamine and/or trialkylphosphine.
Reaction of 4-Bromo-1,2-dimethylbenzene with Various Nucleophiles via Aryne Reaction
Biehl, Edward R.,Razzuk, Aziz,Jovanovic, Misa V.,Khanapure, Subhash P.
, p. 5157 - 5160 (2007/10/02)
4-Bromo-1,2-dimethylbenzene (4a) reacts with a variety of amines, mercaptans, and nitriles under aryne-forming conditions to yield predominantly 4-substituted 1,2-dimethylbenzenes and minor quantities of 3-substituted 1,2-dimethylbenzenes.The product distributions from these reactions are heavily in favor of the 4-substituted isomer since it is formed exclusively from the symmetric 4,5-dimethylbenzyne intermediate (6) and partly from the unsymmetric 3,4-dimethylbenzyne intermediate (5).
