107840-43-7 Usage
Description
(E)-3-AMINO-3-(4-CHLOROPHENYL)-2-PROPENENITRILE, with the molecular formula C9H8ClN3, is a nitrile derivative characterized by a substituted vinyl group and an amino functional group. This chemical compound is structurally similar to existing pharmaceuticals, which makes it a promising candidate for further development and research.
Uses
Used in Pharmaceutical Synthesis:
(E)-3-AMINO-3-(4-CHLOROPHENYL)-2-PROPENENITRILE is used as an intermediate in the synthesis of pharmaceuticals, leveraging its unique chemical structure to contribute to the development of new drugs.
Used in Agrochemical Synthesis:
(E)-3-AMINO-3-(4-CHLOROPHENYL)-2-PROPENENITRILE is also utilized as a building block in the creation of agrochemicals, potentially enhancing the effectiveness of pesticides or other agricultural products.
Used in Organic Chemistry:
(E)-3-AMINO-3-(4-CHLOROPHENYL)-2-PROPENENITRILE serves as a valuable component in organic chemistry, acting as a precursor for the preparation of various chemical compounds due to its reactive functional groups.
Used in Research and Development:
Its potential applications extend to research and development, where it can be employed to study and understand various chemical reactions, contributing to the advancement of chemical knowledge and innovation.
Used in Drug Development:
Owing to its structural similarity with known pharmaceuticals, (E)-3-AMINO-3-(4-CHLOROPHENYL)-2-PROPENENITRILE may be used as a potential drug candidate, particularly in the development of new therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 107840-43-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,8,4 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 107840-43:
(8*1)+(7*0)+(6*7)+(5*8)+(4*4)+(3*0)+(2*4)+(1*3)=117
117 % 10 = 7
So 107840-43-7 is a valid CAS Registry Number.
107840-43-7Relevant articles and documents
Ultrasound-assisted synthesis of β-enaminonitriles in the presence of base
Jagtap, Sachin R.,Bhanushali, Mayur J.,Nandurkar, Nitin S.,Bhanage, Bhalchandra M.
, p. 2253 - 2258 (2007)
Application of ultrasound shows significant rate enhancement for the synthesis of β-enaminonitriles in the presence of base. The role of various homogeneous and heterogeneous bases/solvents was also studied for the reaction, and potassium t-butoxide/t-but
Enantioselective biocatalytic hydrolysis of β-aminonitriles to β-amino-amides using Rhodococcus rhodochrous ATCC BAA-870
Chhiba, Varsha,Bode, Moira L.,Mathiba, Kgama,Kwezi, Wendy,Brady, Dean
experimental part, p. 68 - 74 (2012/04/10)
A range of β-aminonitriles (3-amino-3-phenylpropanenitrile and derivatives) were synthesised by reaction of various benzonitriles with acetonitrile and subsequent reduction of the resulting acrylonitrile products. These compounds were hydrolysed to the co
Rhodium-catalyzed asymmetric hydrogenation of β-acetylamino acrylonitriles
Ma, Miaofeng,Hou, Guohua,Wang, Junru,Zhang, Xumu
experimental part, p. 506 - 511 (2011/06/17)
The rhodium-catalyzed asymmetric hydrogenation of β-acetylamino acrylonitriles was investigated by using monophosphine and bisphosphine ligands. It was found that an Rh-QuinoxP complex exhibited high enantioselectivities for β-aryl substituted β-acetylamino acrylonitriles and the Rh-JosiPhos CyPF-t-Bu complex was proven to be effective for the hydrogenation of tetrasubstituted olefins from cyclic β-acetylamino acrylonitriles.
