13165-67-8 Usage
General Description
Aniline, p-nitro-N-sulfinyl- is an organic compound known for its use in the synthesis of various pharmaceuticals and agrochemicals. It is used as an intermediate in the production of dyes, pharmaceuticals, and agrochemicals. The p-nitro-N-sulfinyl- group on the aniline molecule makes it a valuable building block for the introduction of nitro functionality in organic synthesis. This chemical compound possesses unique reactivity due to the presence of the p-nitro-N-sulfinyl- group, making it an important reagent in the production of various chemical compounds. Additionally, it is important to handle aniline, p-nitro-N-sulfinyl- with caution as it can be toxic and harmful to human health if mishandled.
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
