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(4-nitro-thiobenzoylsulfanyl)-acetic acid is a complex organic chemical compound with the molecular formula C9H7NO5S3. It is characterized by the presence of a 4-nitro-thiobenzoylsulfanyl group attached to an acetic acid moiety. (4-nitro-thiobenzoylsulfanyl)-acetic acid features a nitro group (-NO2) at the para position of the benzene ring, a sulfonyl group (-SO2-), and a thiobenzoyl group (-C6H4-CO-S-). The acetic acid part of the molecule contributes a carboxyl group (-COOH). (4-nitro-thiobenzoylsulfanyl)-acetic acid is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique chemical structure and reactivity. It is important to note that handling and disposal of such chemicals should be done with care, adhering to safety protocols, due to their potential reactivity and toxicity.

1929-01-7

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1929-01-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1929-01-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,2 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1929-01:
(6*1)+(5*9)+(4*2)+(3*9)+(2*0)+(1*1)=87
87 % 10 = 7
So 1929-01-7 is a valid CAS Registry Number.

1929-01-7Relevant 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.

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