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1'-benzylspiro[chromene-2,4'-piperidin]-4(3H)-one oxime is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

693789-31-0

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693789-31-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 693789-31-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,3,7,8 and 9 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 693789-31:
(8*6)+(7*9)+(6*3)+(5*7)+(4*8)+(3*9)+(2*3)+(1*1)=230
230 % 10 = 0
So 693789-31-0 is a valid CAS Registry Number.

693789-31-0Relevant academic research and scientific papers

Synthesis and structural studies of a novel scaffold for drug discovery: A 4,5-dihydro-3H-spiro[1,5-benzoxazepine-2,4′-piperidine]

Willand, Nicolas,Beghyn, Terence,Nowogrocki, Guy,Gesquiere, Jean-Claude,Deprez, Benoit

, p. 1051 - 1054 (2004)

We describe the three-step synthesis of a novel 4,5-dihydro-3H-spiro[1,5- benzoxazepine-2,4′-piperidine] scaffold from ortho-hydroxyacetophenone and N-benzylpiperidone. The structure of one disubstituted derivative, studied by NOESY NMR in an aqueous medi

Discovery of novel SCD1 inhibitors: 5-Alkyl-4,5-dihydro-3H-spiro[1,5- benzoxazepine-2,4′-piperidine] analogs

Uto, Yoshikazu,Ueno, Yuko,Kiyotsuka, Yohei,Miyazawa, Yuriko,Kurata, Hitoshi,Ogata, Tsuneaki,Takagi, Toshiyuki,Wakimoto, Satoko,Ohsumi, Jun

, p. 1892 - 1896 (2011/04/27)

Expansion of the 6-membered ring and subsequent fine-tuning of the newly obtained 7-membered spiropiperidine structure resulted in the discovery of a series of novel and potent SCD1 inhibitors. Preliminary SAR was explored by modifying an alkyl chain on t

BENZO-FUSED OXAZEPINE COMPOUNDS AS STEAROYL-COENZYME A DELTA-9 DESATURASE INHIBITORS

-

Page/Page column 46, (2011/02/24)

The present invention relates to certain 4,5-dihydro-3H-spiro[benzo[b]-[1,4]oxazepine compounds of the Formula (I) or a pharmaceutically acceptable salt thereof, wherein R1, R2, R3, R4, R5, m, n, o, a

A library of novel hydroxamic acids targeting the metallo-protease family: Design, parallel synthesis and screening

Flipo, Marion,Beghyn, Terence,Charton, Julie,Leroux, Virginie A.,Deprez, Benoit P.,Deprez-Poulain, Rebecca F.

, p. 63 - 76 (2007/10/03)

We report here the design and parallel synthesis of 217 compounds based on a malonic-hydroxamic acid template. These compounds are obtained via a two-step solution-phase procedure. The set of diverse building-blocks used makes this strategy suitable for t

Synthesis of new substituted 4,5-dihydro-3H-spiro[1,5]-benzoxazepine-2, 4′-piperidine and biological properties

Laras, Younes,Pietrancosta, Nicolas,Moret, Vincent,Marc, Sylvain,Garino, Cedrik,Rolland, Amandine,Monnier, Valerie,Kraus, Jean-Louis

, p. 812 - 818 (2007/10/03)

The reduction of substituted spiro-piperidinyl chromanone oximes with DIBAH reagents has been known to afford the corresponding substituted 4,5-dihydro-3H-spiro[1,5]-benzoxazepine-2,4?-piperidine. The position and electronic effects of the substituents on

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