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N-(2-nitrophenyl)-5H-dibenzo[d,f][1,3]diazepine-6-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1242020-48-9

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1242020-48-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1242020-48-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,2,0,2 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1242020-48:
(9*1)+(8*2)+(7*4)+(6*2)+(5*0)+(4*2)+(3*0)+(2*4)+(1*8)=89
89 % 10 = 9
So 1242020-48-9 is a valid CAS Registry Number.

1242020-48-9Downstream Products

1242020-48-9Relevant academic research and scientific papers

Synthesis of Dibenzo[ d, f][1,3]Diazepines via Elemental Sulfur-Mediated Cyclocondensation of 2,2′-Biphenyldiamines with 2-Chloroacetic Acid Derivatives

Tikhonova, Tatyana A.,Lyssenko, Konstantin A.,Zavarzin, Igor V.,Volkova, Yulia A.

, p. 15817 - 15826 (2019)

The three-component reaction of 2,2′-biphenyldiamines with 2-chloroacetic acid derivatives and elemental sulfur was developed for the practical synthesis of unknown 2-carboxamide-substituted dibenzo[d,f][1,3]diazepines. This protocol is distinguished by efficiency in water and good tolerance to functional groups and can be adapted to a large-scale synthesis. The chemoselective preparation of a variety of 2-S,N,O-substituted dibenzo[d,f][1,3]diazepines was accomplished using the developed method.

Sulfur-mediated synthesis of unsymmetrically substituted: N -aryl oxalamides by the cascade thioamidation/cyclocondensation and hydrolysis reaction

Ilment, Nikita V.,Lyssenko, Konstantin A.,Tikhonova, Tatyana A.,Volkova, Yulia A.,Zavarzin, Igor V.

, p. 5050 - 5060 (2020/07/30)

A facile and straightforward synthesis of unsymmetrically substituted N-aryl oxalamides from 2,2′-biphenyldiamines, 2-chloroacetic acid derivatives, elemental sulfur, and water has been developed. This protocol is distinguished by efficiency in water under metal-free conditions for N-aryl oxalamides bearing a side-chain NH2-group; it can be adapted for scale-up synthesis. The scope and limitations of this transformation have been investigated.

Synthesis and reactivity of monothiooxamides of the aminonitroarene series

Yarovenko,Polushina,Levchenko,Zavarzin,Krayushkin,Kotovskaya,Charushin

, p. 1276 - 1280 (2010/10/04)

Monothiooxamides containing aminonitrobenzene and aminonitropyridine fragments have been synthesized. A possibility to synthesize thioesters and fused imidazole and diazepine derivatives on their basis has been demonstrated. ; 2009 Springer Science+Busine

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