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1-(4-chlorobenzyl)-1-phenylhydrazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

100712-22-9

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100712-22-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100712-22-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,7,1 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 100712-22:
(8*1)+(7*0)+(6*0)+(5*7)+(4*1)+(3*2)+(2*2)+(1*2)=59
59 % 10 = 9
So 100712-22-9 is a valid CAS Registry Number.

100712-22-9Relevant academic research and scientific papers

Reductive Hydrazination with Trichlorosilane: A Method for the Preparation of 1,1-Disubstituted Hydrazines

Wang, Tao,Di, Xiao,Wang, Chao,Zhou, Li,Sun, Jian

supporting information, p. 1900 - 1903 (2016/05/19)

A straightforward and facile method has been developed to prepare 1,1-disubstituted hydrazines via Lewis base promoted direct reductive hydrazination. Under the catalysis of hexamethylphosphoramide (HMPA) and N,N-dimethylacetamide (DMAc), respectively, various ketones and aldehydes could react with phenylhdrazines to prepare 1,1-disubstituted hydrazines with good to high yields.

2,3′-Bis(1′H-indole) heterocycles: New p53/MDM2/MDMX antagonists

Neochoritis, Constantinos G.,Wang, Kan,Estrada-Ortiz, Natalia,Herdtweck, Eberhardt,Kubica, Katarzyna,Twarda, Aleksandra,Zak, Krzysztof M.,Holak, Tad A.,D?mling, Alexander

supporting information, p. 5661 - 5666 (2015/11/24)

The protein-protein interaction of p53 and MDM2/X is a promising non genotoxic anticancer target. A rapid and efficient methodology was developed to synthesize the 2,3′-bis(1′H-indole) heterocyclic scaffold 2 as ester, acid and amide derivatives. Their binding affinity with MDM2 was evaluated using both fluorescence polarization (FP) assay and HSQC experiments, indicating good inhibition and a perfect starting point for further optimizations.

A convenient synthesis of 1-alkyl-1-phenylhydrazines from N-aminophthalimide

Nara, Shigeru,Sakamoto, Takeshi,Miyazawa, Etsuko,Kikugawa, Yasuo

, p. 87 - 98 (2007/10/03)

N-Alkylaminophthalimides were synthesized by condensation of N-aminophthalimide with aldehydes, and subsequent reduction of the intermediate with pyridine-borane in acetic acid. N-Phenylation and removal of the phthalimide group gave 1-alkyl-1-phenylhydrazines in high yield.

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