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89042-13-7

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89042-13-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89042-13-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,0,4 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 89042-13:
(7*8)+(6*9)+(5*0)+(4*4)+(3*2)+(2*1)+(1*3)=137
137 % 10 = 7
So 89042-13-7 is a valid CAS Registry Number.

89042-13-7Relevant academic research and scientific papers

Catalytic Staudinger Reduction at Room Temperature

Lenstra, Danny C.,Wolf, Joris J.,Mecinovi?, Jasmin

, p. 6536 - 6545 (2019)

We report an efficient catalytic Staudinger reduction at room temperature that enables the preparation of a structurally diverse set of amines from azides in excellent yields. The reaction is based on the use of catalytic amounts of triphenylphosphine as a phosphine source and diphenyldisiloxane as a reducing agent. Our catalytic Staudinger reduction exhibits a high chemoselectivity, as exemplified by reduction of azides over other common functionalities, including nitriles, alkenes, alkynes, esters, and ketones.

Sustainable organophosphorus-catalysed Staudinger reduction

Lenstra, Danny C.,Lenting, Peter E.,Mecinovi?, Jasmin

, p. 4418 - 4422 (2018/10/17)

A highly efficient and sustainable catalytic Staudinger reduction for the conversion of organic azides to amines in excellent yields has been developed. The reaction displays excellent functional group tolerance to functionalities that are otherwise prone to reduction, such as sulfones, esters, amides, ketones, nitriles, alkenes, and benzyl ethers. The green nature of the reaction is exemplified by the use of PMHS, CPME, and a lack of column chromatography.

METHODS AND COMPOSITIONS FOR SELECTIVE AND TARGETED CANCER THERAPY

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Page/Page column 228, (2015/03/28)

Provided herein are methods and compositions for selective and targeted cancer therapy, in particular certain benzothiophenes, benzothiazoles, oxalamides, N-acyl ureas and chromones, and their use in selectively treating certain adenocarcinomas. In some embodiments, the selective toxicity of the compounds may be mediated through SCD1 and/or CYP450 such as CYP4F11.

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