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1-Propanone, 1-(4-chlorophenyl)-3-(phenylamino)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

19832-75-8

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19832-75-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19832-75-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,8,3 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 19832-75:
(7*1)+(6*9)+(5*8)+(4*3)+(3*2)+(2*7)+(1*5)=138
138 % 10 = 8
So 19832-75-8 is a valid CAS Registry Number.

19832-75-8Relevant academic research and scientific papers

I2-Promoted Intramolecular Oxidative Cyclization of Butenyl Anilines: A Facile Route to Benzo[b]azepines

An, Zhenyu,Ren, Yi,Liu, Yafeng,Yan, Rulong

, p. 2614 - 2617 (2021/08/06)

A metal-free approach for the synthesis of seven-membered N-heterocycles has been developed by the I2-promoted intramolecular cross-coupling/annulation of butenyl anilines. This cyclization reaction involves C?H activation and C?C bond formation and exhibits good functional group tolerance. A series of benzo[b]azepine derivatives are obtained in moderate to good yields.

Construction of N-Alkyl- and N-Arylaziridines from Unprotected Amines via C-H Oxidative Amination Strategy

Yu, Yang,Li, Meijuan,Zhang, Yong,Liu, Yonghai,Shi, Lei,Wang, Wei,Li, Hao

supporting information, p. 904 - 907 (2019/05/16)

A copper-promoted intramolecular C-H oxidative amination reaction between secondary amine (N-H) and C(sp3)-H at the benzylic position of azaarenes or α-position of ketones for the synthesis of aziridine derivatives has been developed. Moreover,

Synthesis of Heterocyclic Compounds: Part XXVIII - Potential Antileukemic Agents from 3,4-Dihydro-1,3,2-oxazaphosphorin-2-oxides

Sahasrabudhe, S. D.,Tilak, B. D.

, p. 914 - 917 (2007/10/02)

Some 3,6-diaryl-2-chloro-3,4-dihydro-1,3,2-oxazaphosphorin-2-oxides (4a-q, 6a-e and 7a, b) have been synthesised and tested for their anti-leukemic activity.

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