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malonyl dihydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16501-77-2

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16501-77-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16501-77-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,5,0 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 16501-77:
(7*1)+(6*6)+(5*5)+(4*0)+(3*1)+(2*7)+(1*7)=92
92 % 10 = 2
So 16501-77-2 is a valid CAS Registry Number.

16501-77-2Relevant academic research and scientific papers

Syntheses and antitumor activities of N′1, N′3-dialkyl-N′1,N′3-di- (alkylcarbonothioyl) malonohydrazide: The discovery of elesclomol

Chen, Shoujun,Sun, Lijun,Koya, Keizo,Tatsuta, Noriaki,Xia, Zhiqiang,Korbut, Timothy,Du, Zhenjian,Wu, Jim,Liang, Guiqing,Jiang, Jun,Ono, Mitsunori,Zhou, Dan,Sonderfan, Andrew

, p. 5070 - 5076 (2013/09/12)

A series of N′1,N′3-dialkyl- N′1,N′3-di(alkylcarbonothioyl) malonohydrazides have been designed and synthesized as anticancer agents by targeting oxidative stress and Hsp70 induction. Structure-activity relationship (SAR) studies lead to the discovery of STA-4783 (elesclomol), a novel small molecule that has been evaluated in a number of clinical trials as an anticancer agent in combination with Taxol.

A Convenient Synthesis of Alkyl and Aryl Substituted Bis-1,3,4-oxadiazoles

Al-Talib, Mahmoud,Tashtoush, Hasan,Odeh, Nedal

, p. 1811 - 1817 (2007/10/02)

Substituted bis-1,3,4-oxadiazoles 3a-l have been synthesized from the cyclization of N,N'-diaroyl or N,N'-dialkanoyl diacyl hydrazides, in presence of phosphorus oxychloride.All new compounds have been identified by 1H-NMR, 13C-NMR and elemental analysis.

Reference Data - Diacyl Acid Dihydrazides

Al-Talib, Mahmoud,Tashtoush, Hasan,Odeh, Nedal

, p. 1072 - 1075 (2007/10/02)

N,N'-Diacyl acid dihydrazides were prepared by the reaction of acid dihydrazides with two equivalents of acyl chlorides.The structure of these compounds were elucidated by 1H and 13C NMR spectroscopy.

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