67083-70-9 Usage
General Description
[(2,3-dimethylphenyl)amino]acetonitrile is a chemical compound with the molecular formula C10H12N2. It is a colorless to light yellow liquid with a faint odor, and it is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. The compound is a member of the class of nitriles and contains an acetonitrile group, as well as a 2,3-dimethylphenylamino group. It is often utilized in the production of dyes, pigments, and other organic compounds. The chemical's properties and potential applications make it a valuable building block in various industrial processes. However, it is important to handle and store this compound safely, as it can be harmful if ingested, inhaled, or comes into contact with the skin or eyes.
Check Digit Verification of cas no
The CAS Registry Mumber 67083-70-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,0,8 and 3 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 67083-70:
(7*6)+(6*7)+(5*0)+(4*8)+(3*3)+(2*7)+(1*0)=139
139 % 10 = 9
So 67083-70-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H12N2/c1-8-4-3-5-10(9(8)2)12-7-6-11/h3-5,12H,7H2,1-2H3
67083-70-9Relevant articles and documents
Iron-catalyzed reductive strecker reaction
Yan, Fachao,Huang, Zijun,Du, Chen-Xia,Bai, Jian-Fei,Li, Yuehui
, p. 188 - 194 (2021/02/03)
Strecker reaction is widely applied for the synthesis of amino acids from aldehydes, amines and cyanides. Herein, we report the FeI2-catalyzed reductive Strecker type reaction of formamides instead of aldehydes to produce amino acetonitriles. The challenging capture of carbinolamine intermediates by CN? was achieved via Fe catalysis. This approach afforded better yields than the use of Ir- or Rh-catalysts. The application ability of this methodology is demonstrated by 1) one-pot construction of (13C labeled) complex molecules from CO2 via amino acetonitrile intermediates and 2) convenient production of homologated carboxylic acids from aldehydes.
