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(Z)-3-cyano-3-phenylacrylic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

756790-25-7

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756790-25-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 756790-25-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,6,7,9 and 0 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 756790-25:
(8*7)+(7*5)+(6*6)+(5*7)+(4*9)+(3*0)+(2*2)+(1*5)=207
207 % 10 = 7
So 756790-25-7 is a valid CAS Registry Number.

756790-25-7Downstream Products

756790-25-7Relevant academic research and scientific papers

Discovery of Novel Celastrol Derivatives as Hsp90-Cdc37 Interaction Disruptors with Antitumor Activity

Li, Na,Xu, Manyi,Wang, Bing,Shi, Zhixian,Zhao, Zihao,Tang, Yunqing,Wang, Xinyue,Sun, Jianbo,Chen, Li

, p. 10798 - 10815 (2019)

To develop novel and efficient heat shock protein 90-cell division cycle 37 (Hsp90-Cdc37) interaction disruptors, several lipophilic fragments were introduced into celastrol (CEL) to synthesize 48 new CEL derivatives. Among all the target compounds, 41 wa

Design, synthesis and SARs of novel telomerase inhibitors based on BIBR1532

Chen, Fei Hu,Liu, Chao,Liu, Xin Hua,Sheng, Xiao Bao,Zhou, Hua

, (2020/07/21)

Telomerase has become one of the new popular targets for the development of anti-tumor drugs. Based on the structural characteristics of the BIBR1532 which has entered the stage of clinical research, six series total of 64 new compounds with diverse struc

Synthesis of coumarins via PIDA/I2-mediated oxidative cyclization of substituted phenylacrylic acids

Li, Jinming,Chen, Huiyu,Zhang-Negrerie, Daisy,Du, Yunfei,Zhao, Kang

, p. 4311 - 4320 (2013/04/24)

A variety of functionalized coumarins were synthesized from substituted phenylacrylic acids via PIDA/I2-mediated and irradiation-promoted oxidative carbon-oxygen bond formation. Our studies show that the oxygen in the pendant carboxylic acid group cyclizes favorably to the aryl ring that is cis to it. The main advantages of this method include good functional group tolerance and the transition-metal-free characteristic. The Royal Society of Chemistry 2013.

A short, chemoenzymatic route to chiral β-aryl-γ-amino acids using reductases from anaerobic bacteria

Fryszkowska, Anna,Fisher, Karl,Gardiner, John M.,Stephens, Gill M.

supporting information; experimental part, p. 533 - 535 (2010/05/11)

A short chemoenzymatic synthesis of β-aryl-γ-aminobutyric acids has been developed, based on a highly enantioselective biocatalytic reduction of β-aryl-β-cyano-α,β-unsaturated carboxylic acids.

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