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(S)-2-Cyclohexyl-1-((4R,5S)-5-isobutyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-ethylamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

131550-34-0

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131550-34-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 131550-34-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,5,5 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 131550-34:
(8*1)+(7*3)+(6*1)+(5*5)+(4*5)+(3*0)+(2*3)+(1*4)=90
90 % 10 = 0
So 131550-34-0 is a valid CAS Registry Number.

131550-34-0Relevant academic research and scientific papers

Dipeptide Isosteres. 1. Synthesis of Dihydroxyethylene Dipeptide Isosteres via Diastereoselective Additions of Alkyllithium Reagents to N,N-Dimethylhydrazones. Preparation of Renin and HIV-1 Protease Inhibitor Transition-State Mimics

Baker, William R.,Condon, Stephen L.

, p. 3277 - 3284 (2007/10/02)

The amino and diamino dihydroxyethylene dipeptide isosteres 19a,b and 23 are important intermediates for the preparation of inhibitors of human renin and HIV-1 protease, respectively.A general synthetic strategy was developed to access both dipeptide isos

A practical synthesis of the dihydroxyethylene dipeptide isostere, (2S, 3R, 4S) 2-[(tert-butyloxycarbonyl)amino]-1-cyclohexyl-3,4-dihydroxy-6-methylheptane, from D-isoascorbic acid

Baker, William R.,Condon, Stephen L.

, p. 1581 - 1584 (2007/10/02)

The N-Boc dihydroxyethylene dipeptide isostere 7 and its N-Boc 3-(thiazol-4-yl)alanyl derivative 8 were synthesized, without purification of intermediates, from (4S,5R)-2,2-dimethyl-4-(2-methylpropyl)-5-hydroxymethyl-1,3-dioxolane (3b), in 24 and 32% over

A Versatile, Efficient Synthesis of (-)-(2S, 3R, 4S)-2-Amino-1-cyclohexyl-3,4-dihydroxy-6-methylheptane, The Abbott Pseudodipeptidyl Insert

Wood, John L.,Jones, David R.,Hirschmann, Ralph,Smith, Amos B.

, p. 6329 - 6330 (2007/10/02)

An economic construction (6 steps, 36percent yield) of a valuable peptide analog subunit, the Abbott pseudodipeptidyl insert (-)-(2S,3R,4S)-2-amino-1-cyclohexyl-3,4-dihydroxy-6-methylheptane (1), has been developed.

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