13165-67-8 Usage
Description
Aniline, p-nitro-N-sulfinylis an organic compound that serves as a crucial intermediate in the synthesis of pharmaceuticals, agrochemicals, and dyes. The presence of the p-nitro-N-sulfinylgroup endows it with unique reactivity, making it a valuable building block for introducing nitro functionality in organic synthesis. Its applications are diverse, but it must be handled with care due to its potential toxicity and harmful effects on human health.
Uses
Used in Pharmaceutical Industry:
Aniline, p-nitro-N-sulfinylis used as a key intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
Aniline, p-nitro-N-sulfinylis utilized as an intermediate in the production of agrochemicals, playing a role in the creation of pesticides and other agricultural products to protect crops and enhance yields.
Used in Dye Industry:
Aniline, p-nitro-N-sulfinylis employed as a building block in the synthesis of dyes, contributing to the coloration and enhancement of various materials in the textile and other industries.
Used in Organic Synthesis:
Due to its unique reactivity, Aniline, p-nitro-N-sulfinylis used as a reagent in organic synthesis, facilitating the introduction of nitro functionality in the production of a wide range of chemical compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 13165-67-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,6 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13165-67:
(7*1)+(6*3)+(5*1)+(4*6)+(3*5)+(2*6)+(1*7)=88
88 % 10 = 8
So 13165-67-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H4N2O3S/c9-8(10)6-3-1-5(2-4-6)7-12-11/h1-4H
13165-67-8Relevant articles and documents
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Kobayashi,Honda
, p. 1778,1781 (1966)
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Reaction of electron-deficient N-sulfinylanilines with chiral α-hydroxy acids: A new process for the synthesis of enantiomerically pure α-hydroxy amides
Chidambaram,Zhu,Penmetsa,Kronenthal,Kant
, p. 6017 - 6020 (2007/10/03)
A practical procedure to prepare enantiomerically pure α-hydroxy amides from chiral α-hydroxy acids and electron-deficient anilines via N-sulfinylaniline derivatives has been developed. (C) 2000 Elsevier Science Ltd.
NEW FACILE SYNTHESIS OF N-SULFINYLAMINE DERIVATIVES USING N,N'-SULFINYLBISIMIDAZOLE AND N-(CHLOROSULFINYL)IMIDAZOLE
Kim, Yong Hae,Shin, Jai Moo
, p. 3821 - 3824 (2007/10/02)
Treatment of amine derivatives such as amines, sulfonamides, and amides with N,N'-sulfinylbisimidazole (1) and N-(chlorosulfinyl)imidazole (2) in situ respectively gives the corresponding N-sulfinylamine derivatives (3): the latter reaction using N-(chlor
