131019-17-5 Usage
Nitrile derivative
2-(4'-methoxycarbonylphenyl)propanenitrile is a derivative of nitriles, which are compounds containing the cyano group (C≡N).
Phenyl group with a methoxy carbonyl substituent
The compound contains a phenyl group (a six-carbon ring with delocalized electrons) that has a methoxy group (-OCH3) attached to it, which influences its chemical properties.
Propanenitrile moiety
The compound also contains a propanenitrile group (a three-carbon chain with a cyano group at one end and a double bond between the first and second carbons).
Versatile reactivity
2-(4'-methoxycarbonylphenyl)propanenitrile can undergo a variety of chemical reactions, making it useful in organic synthesis.
Potential pharmaceutical applications
The compound has potential as a building block for the development of new pharmaceuticals due to its structural features and reactivity.
Valuable building block
The compound's structural features make it suitable for various transformations and functionalizations, making it a valuable building block for the synthesis of novel compounds.
Potentially useful for the development of bioactive molecules
The presence of the nitrile group makes 2-(4'-methoxycarbonylphenyl)propanenitrile potentially useful for the development of bioactive molecules targeting specific biological pathways.
Check Digit Verification of cas no
The CAS Registry Mumber 131019-17-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,0,1 and 9 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 131019-17:
(8*1)+(7*3)+(6*1)+(5*0)+(4*1)+(3*9)+(2*1)+(1*7)=75
75 % 10 = 5
So 131019-17-5 is a valid CAS Registry Number.
131019-17-5Relevant articles and documents
Rapid and Simple Access to α-(Hetero)arylacetonitriles from Gem-Difluoroalkenes
Hu, Dandan,Liu, Jiayue,Ren, Hongjun,Song, Jinyu,Zhang, Jun-Qi,Zhu, Guorong
supporting information, p. 786 - 790 (2022/01/28)
A scalable cyanation of gem-difluoroalkenes to (hetero)arylacetonitrile derivatives was developed. This strategy features mild reaction conditions, excellent yields, wide substrate scope, and broad functional group tolerance. Significantly, in this reacti
Efficient nickel-catalyzed hydrocyanation of alkenes using acetone cyanohydrin as a safer cyano source
Nemoto, Koji,Nagafuchi, Tsuyoshi,Tominaga, Ken-ichi,Sato, Kazuhiko
, p. 3199 - 3203 (2016/07/06)
An active nickel catalyst prepared in situ from a Ni(II) compound, phosphine ligand, and zinc powder was found to be an efficient catalyst system for the hydrocyanation of various alkenes using acetone cyanohydrin as a safer cyano source. The combination of NiCl2·6H2O and 1,3-bis(diphenylphosphino)propane was the most efficient catalyst precursor in DMF. Under the optimized conditions, various styrenes, heterocyclic alkenes, and aliphatic alkenes were converted to their corresponding nitriles in excellent yields.
β-Amination of saturated nitriles through palladium-catalyzed dehydrogenation, 1,4-addition, and re-dehydrogenation
Ueno, Satoshi,Maeda, Ryohei,Yasuoka, Shohei,Kuwano, Ryoichi
supporting information, p. 40 - 42 (2013/02/25)
Amination at the β-position of 2-arylpropionitriles through catalytic dehydrogenation occurred by using [PdCl2(PMe3) 2] catalyst and bromobenzene. This is the first catalytic reaction involving the direct dehydrogenation of saturated nitriles.
