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(1S,3S,4S,5R,6R,7R)-1-((4S,5R)-4-Acetoxy-5-methyl-3-methylene-6-phenyl-hexyl)-6-((E)-(4S,6S)-4,6-dimethyl-oct-2-enoyloxy)-4,7-dihydroxy-2,8-dioxa-bicyclo[3.2.1]octane-3,4,5-tricarboxylic acid 4,5-di-tert-butyl ester 3-methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

144571-48-2

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144571-48-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144571-48-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,5,7 and 1 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 144571-48:
(8*1)+(7*4)+(6*4)+(5*5)+(4*7)+(3*1)+(2*4)+(1*8)=132
132 % 10 = 2
So 144571-48-2 is a valid CAS Registry Number.

144571-48-2Downstream Products

144571-48-2Relevant academic research and scientific papers

The squalestatins: Synthesis of C-4 carboxamide derivatives

Chan, Chuen,Scicinski, Jan J.,Srikantha, Anton R. P.,Watson, Nigel S.

, p. 8925 - 8928 (2007/10/03)

Synthesis of squalestatin S1 C-4 carboxamide, 2, as well as related C-4 amides and C-4 hydroxymethyl derivatives possessing a C-3 hydroxymethyl group (15 and 19) together with their SQS inhibitory activities are presented. Copyright (C) 1996 Elsevier Science Ltd.

The squalestatins: Inhibitors of squalene synthase. Enzyme inhibitory activities and in vivo evaluation of C3-modified analogues

Procopiou, Panayiotis A.,Cox, Brian,Kirk, Barrie E.,Lester, Michael G.,McCarthy, Alun D.,Sareen, Meenu,Sharratt, Peter J.,Snowden, Michael A.,Spooner, Stephen J.,Watson, Nigel S.,Widdowson, Julia

, p. 1413 - 1422 (2007/10/03)

Squalestatin analogues modified at C3 were prepared and evaluated for their ability to inhibit rat liver microsomal squalene synthase in vitro. While the 4,6-dimethyloctenoate ester group at C6 was maintained, a number of modifications to the C3 carboxyli

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