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1,4-Dioxaspiro[4.5]dec-7-ene-7-carboxylic acid, 8-[[(1S)-1-phenylethyl]amino]-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

158436-80-7

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158436-80-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 158436-80-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,4,3 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 158436-80:
(8*1)+(7*5)+(6*8)+(5*4)+(4*3)+(3*6)+(2*8)+(1*0)=157
157 % 10 = 7
So 158436-80-7 is a valid CAS Registry Number.

158436-80-7Relevant academic research and scientific papers

ENANTIOSELECTIVE SYNTHESIS OF SUBSTITUTED OCTALONES

Sequeira, Lucia C.,Costa, Paulo R. R.,Neves, Alexandre,Esteves, Pierre

, p. 1433 - 1434 (1994)

The octalones (R)-(-)-1a and (S)-(-)-1b were prepared from the Michael adducts 7a and 7b respectively.These intermediates were obtained by the "deracemizing alkylation" of cyclanones 3a and 3b.

Stereoselective Bulk Synthesis of CCR2 Antagonist BMS-741672: Assembly of an All-cis (S,R,R)-1,2,4-Triaminocyclohexane (TACH) Core via Sequential Heterogeneous Asymmetric Hydrogenations

Deerberg, Joerg,Prasad, Siva J.,Sfouggatakis, Chris,Eastgate, Martin D.,Fan, Yu,Chidambaram, Ramakrishnan,Sharma, Praveen,Li, Li,Schild, Richard,Müslehiddino?lu, Jale,Chung, Hyei-Jha,Leung, Simon,Rosso, Victor

, p. 1949 - 1966 (2017/02/10)

A concise bulk synthesis of stereochemically complex CCR2 antagonist BMS-741672 is reported. A distinct structural feature is the chiral all-cis 1,2,4-triaminocyclohexane (TACH) core, which was assembled through consecutive stereocontrolled heterogeneous

γ-Lactams as glycinamide replacements in cyclohexane-based CC chemokine receptor 2 (CCR2) antagonists

Cherney, Robert J.,Mo, Ruowei,Meyer, Dayton T.,Voss, Matthew E.,Yang, Michael G.,Santella III, Joseph B.,Duncia, John V.,Lo, Yvonne C.,Yang, Gengjie,Miller, Persymphonie B.,Scherle, Peggy A.,Zhao, Qihong,Mandlekar, Sandhya,Cvijic, Mary Ellen,Barrish, Joel C.,Decicco, Carl P.,Carter, Percy H.

scheme or table, p. 2425 - 2430 (2010/08/05)

We describe the design, synthesis, and evaluation, of γ-lactams as glycinamide replacements within a series of di- and trisubstituted cyclohexane CCR2 antagonists. The lactam-containing trisubstituted cyclohexanes proved to be more potent than the disubst

Cyclic derivatives as modulators of chemokine receptor activity

-

Page/Page column 108, (2008/06/13)

The present application describes modulators of MCP-1 of formula (I): or pharmaceutically acceptable salt forms thereof, useful for the treatment of rheumatoid arthritis, multiple sclerosis, atherosclerosis and asthma.

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