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α-<2-Nitro-5-(methylthio)phenyl>acetonitrile is a chemical compound with the molecular formula C9H8N2O2S. It is an aromatic nitrile derivative, characterized by the presence of a nitro group (-NO2) at the 2nd position and a methylthio group (-SCH3) at the 5th position on the phenyl ring. The molecule also contains an acetonitrile group (-CH2CN) attached to the alpha carbon of the phenyl ring. α-<2-Nitro-5-(methylthio)phenyl>acetonitrile is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as an intermediate in the production of dyes and pigments. Due to its reactivity and functional groups, it is essential to handle α-<2-Nitro-5-(methylthio)phenyl>acetonitrile with care, following proper safety protocols.

72301-70-3

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72301-70-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72301-70-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,3,0 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 72301-70:
(7*7)+(6*2)+(5*3)+(4*0)+(3*1)+(2*7)+(1*0)=93
93 % 10 = 3
So 72301-70-3 is a valid CAS Registry Number.

72301-70-3Downstream Products

72301-70-3Relevant academic research and scientific papers

NOVEL HETEROCYCLIC COMPOUNDS AND USE THEREOF IN MEDICINE AND IN COSMETICS

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Paragraph 1158, (2018/03/25)

The invention relates to novel heterocyclic compounds of general formula (I), as well as their pharmaceutically acceptable salts, and their enantiomers. The invention also relates to the use thereof as a medicinal product, preferably in the prevention and/or treatment of inflammatory diseases with a neurogenic component or use thereof as a cosmetic. The compounds of the present invention act as antagonists of the CGRP-R receptor.

Vicarious Nucleophilic Substitution of Hydrogen in Nitroarenes with α-Substituted Nitriles and Esters. Direct α-Cyanoalkylation and α-Carbalkoxyalkylation of Nitroarenes

Makosza, Mieczyslaw,Winiarski, Jerzy

, p. 1494 - 1499 (2007/10/02)

Carbanions generated from alkanenitriles bearing α-chloro, α-OR, or α-SR groups and from aliphatic esters bearing α-SR groups react with mononitroarenes to replace hydrogen atoms of the nitroaromatic ring ortho or para to the nitro group with α-cyanoalkyl or α-carbalkoxyalkyl substituents.The nucleophilic replacement of hydrogen with such carbanions proceeds faster than substitution of halogen ortho or para to the nitro group.

Vicarious Substitution of Hydrogen in Aromatic Nitro Compounds with Acetonitrile Derivatives

Makosza, Mieczyslaw,Winiarski, Jerzy

, p. 1534 - 1535 (2007/10/02)

Carbanions of α-phenoxy and thioalkoxy nitriles substitute hydrogen in the para or ortho position of aromatic nitro compounds, giving nitroarylacetonitriles in a process in which phenolate or thiolate anions are vicarious leaving groups.

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