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2-methoxyimino-3-phenylpropionic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

35031-41-5

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35031-41-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35031-41-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,0,3 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 35031-41:
(7*3)+(6*5)+(5*0)+(4*3)+(3*1)+(2*4)+(1*1)=75
75 % 10 = 5
So 35031-41-5 is a valid CAS Registry Number.

35031-41-5Relevant academic research and scientific papers

Assembly of indoline-2-carboxylate-embodied dipeptides via Pd-catalyzed C(sp2)-H bond direct functionalization

He, Yu-Peng,Zhang, Chao,Fan, Mengyang,Wu, Zhijie,Ma, Dawei

, p. 496 - 499 (2015)

Intramolecular dehydrogenative cyclization of 2-methoxyiminoacyl-protected phenylalanine derivatives proceeded at 110 ?°C under catalysis of Pd(OAc)2 in the presence of 1-fluoro-2,4,6-trimethylpyridinium tetrafluoroborate to afford substituted

Synthesis and activity evaluation of the cyclic dipeptides arylidene N-alkoxydiketopiperazines

Tian, Xia,Feng, Juan,Fan, Shi-ming,zhen, Xiao-li,Han, Jian-rong,Liu, Shou-xin

, p. 5197 - 5205 (2016/10/24)

A series of arylidene N-alkoxydiketopiperazines was designed and stereoselectively synthesized via oxime-ether formation and intramolecular acylation. Possible cyclization and acid-catalyzed rearrangement-fragmentation mechanisms were discussed. The crystal structure of the novel diketopiperazine further confirmed the rearrangement mechanism. Most compounds exhibited antitumor activity. Several compounds were more potent against caspase-3. Specifically, compounds 6e, 6g, and 6f inhibited caspase-3 at IC50values lying within the low micromolar range and demonstrated good selectivity. The binding modes of alkoxydiketopiperazines in the active center of caspase-3 were also discussed based on the molecular docking results.

Design, synthesis, and antitumor activity of novel acylate of 6-OH at 1- O-acetylbritannilactone

Liu, Shouxin,Feng, Jun,Liu, He,Li, Junzhang,Tian, Xia

, p. 200 - 205 (2015/04/14)

N-(α-Alkyloxime-3-phenylpropionyl) proline was designed and synthesized as an acylating agent to modify the 6-OH of 1-O-acetylbritannilactone. Eight intermediates and eight target compounds were obtained. The structures of sixteen novel compounds were characterized by 1HNMR, IR and HRMS. The activities against HL-60 and Bel-7402 cell lines were tested, the IC50 values of compound IVg were 2.7 μM and 4.3 μM, respectively.

Stereoselective synthesis and rearrangement-fragmentation of arylidene N-alkoxydiketopiperazines

Liu, Shouxin,Mu, Yun,Han, Jianrong,Zhen, Xiaoli,Yang, Yihua,Tian, Xia,Whiting, Andrew

experimental part, p. 7476 - 7481 (2011/12/03)

A stereoselective synthesis of arylidene N-alkoxydiketopiperazines via oxime-ether formation and intramolecular acylation is described, followed by an acid-catalysed rearrangement-fragmentation to give novel diketopiperazine hemiaminal derivatives with us

Design, synthesis, and anti-tumor activity of (2-O-alkyloxime-3-phenyl)- propionyl-1-O-acetylbritannilactone esters

Liu, Shouxin,Liu, He,Yan, Weiying,Zhang, Li,Bai, Naisheng,Ho, Chi-Tang

, p. 2783 - 2789 (2007/10/03)

The extracts of Inula britannica have anti-inflammatory, anti-bacterial, anti-hepatitic, and anti-tumor activities. Various sesquiterpene lactones with cytotoxic properties including 1-O-acetylbritannilactone (1) have been isolated from this Chinese medic

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