63086-19-1 Usage
Appearance
White to off-white solid The compound is a solid with a white to off-white color.
Usage
Intermediate in pharmaceutical and agrochemical synthesis It is commonly used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals.
Classification
Acetonitrile derivative The compound is classified as an acetonitrile derivative, which means it is derived from acetonitrile.
Chemical structure
Benzene ring with chlorine and amino group The compound contains a benzene ring with a chlorine atom attached to one of the carbon atoms and an amino group attached to the benzene ring.
Organic synthesis
Mild and versatile reactions 2-[(4-chlorophenyl)methyl]aminoacetonitrile is known for its mild and versatile reactions in organic synthesis.
Potential applications
Medicinal chemistry and drug development The compound may have potential applications in the field of medicinal chemistry and drug development.
Check Digit Verification of cas no
The CAS Registry Mumber 63086-19-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,0,8 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 63086-19:
(7*6)+(6*3)+(5*0)+(4*8)+(3*6)+(2*1)+(1*9)=121
121 % 10 = 1
So 63086-19-1 is a valid CAS Registry Number.
63086-19-1Relevant articles and documents
Cs2CO3-Promoted Direct N-Alkylation: Highly Chemoselective Synthesis of N-Alkylated Benzylamines and Anilines
Castillo, Juan-Carlos,Orrego-Hernández, Jessica,Portilla, Jaime
, p. 3824 - 3835 (2016/08/20)
Herein is described an efficient and chemoselective method for the synthesis of diversely substituted secondary amines in yields up to 98 %. Direct mono-N-alkylation of primary benzylamines and anilines with a wide range of alkyl halides is promoted by a cesium base in the absence of any additive or catalyst. The basicity and solubility of cesium carbonate in anhydrous N,N-dimethylformamide not only enables mono-N-alkylation of primary amines but also suppresses undesired dialkylation of the desired amines.
