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8-Hydroxymethyl-des-AB-cholest-8-ene p-nitrobenzoate is a complex organic compound with the molecular formula C34H51NO4. It is derived from cholest-8-ene, a steroidal compound, and features a hydroxymethyl group at the 8-position. The "des-AB" part of the name indicates that the compound lacks the A and B rings typically found in cholesterol. The p-nitrobenzoate group is an ester derived from p-nitrobenzoic acid, which is attached to the hydroxymethyl group. 8-hydroxymethyl-des-AB-cholest-8-ene p-nitrobenzoate is often used in biochemical research as a substrate for enzymes, particularly those involved in steroid metabolism, due to its unique structure and reactivity. It serves as a model for studying enzyme kinetics and mechanisms, providing insights into the catalytic processes of these enzymes.

3752-57-6

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3752-57-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3752-57-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,5 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3752-57:
(6*3)+(5*7)+(4*5)+(3*2)+(2*5)+(1*7)=96
96 % 10 = 6
So 3752-57-6 is a valid CAS Registry Number.

3752-57-6Relevant academic research and scientific papers

Synthesis of 8-methylene-des-AB-cholestan-9-one by cholesterol degradation

Morzycki, Jacek W.,Jurek, Jaroslaw,Rodewald, Wladyslaw J.

, p. 1540 - 1543 (2007/10/02)

The short synthetic route from 3β-acetoxy-5β-methyl-19-norcholest-9(10)-en-6-one (1) to 8-methylene-des-AB-cholestan-9-one (8) is described.Compound 8 is a convenient intermediate for synthesis of relatives of vitamin D3 by the A CD route.

Calciferol and its Relatives. Part 26. A Conversion of Cholesterol into 8-Hydroxymethyl-des-AB-cholest-8-ene

Kocienski, Philip J.,Lythgoe, Basil,Roberts, David A.

, p. 897 - 901 (2007/10/02)

The methoxy-ketone (7), derived from Westphalen's diol, was degraded to 8α-benzoyloxymethyl-des-AB-cholestan-9-one (10), from which the title compound (6) was obtained in a yield of 47percent based on the ketone (7), or 22.5percent overall from cholestero

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