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2α-methyl-5α-cholestan-3-one is a steroidal ketone derived from cholesterol, characterized by the presence of a methyl group at the 2α position and a ketone group at the 3 position. 2α-methyl-5α-cholestan-3-one is a member of the cholestane family, which are cyclic hydrocarbons with a fused ring structure. It is an important intermediate in the synthesis of various steroids and has potential applications in the pharmaceutical industry, particularly in the development of drugs targeting hormonal imbalances and other steroid-related conditions. The chemical structure of 2α-methyl-5α-cholestan-3-one is defined by its unique arrangement of carbon atoms, which contributes to its specific biological activities and chemical properties.

2097-78-1

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2097-78-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2097-78-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,9 and 7 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2097-78:
(6*2)+(5*0)+(4*9)+(3*7)+(2*7)+(1*8)=91
91 % 10 = 1
So 2097-78-1 is a valid CAS Registry Number.

2097-78-1Relevant academic research and scientific papers

Regio- and stereospecific synthesis of cholesterol derivatives and their hormonal activity in Caenorhabditis elegans

Schmidt, Arndt W.,Doert, Thomas,Goutal, Sigrid,Gruner, Margit,Mende, Fanny,Kurzchalia, Teymuras V.,Knoelker, Hans-Joachim

, p. 3687 - 3706 (2007/10/03)

Cholesterol is essential for the survival of the nematode Caenorhabditis elegans. Recent studies have demonstrated that cholesterol derivatives regulate two processes in the life cycle of worms: controlling molting and inducing a specialized non-feeding larval stage. However, the chemical structure of the cholesterol-derived signalling molecules for these or any other functions has not yet been identified. Herein, we describe the regio- and stereospecific synthesis of a number of cholesterol derivatives. The lithium-ammonia reduction of 4-cholesten-3-one was utilized to develop a general method for the introduction of diverse functional groups at C-4α of 5α-cholestan- 3β-ol. Stereoselective functionalization at C-7 was achieved starting from 7-ketocholesterol derivatives. 6-Keto-5α-cholestan-3β-ol was utilized for specific functionalizations at C-6 and C-7. The structure-activity relationships of the different cholesterol derivatives have been investigated by feeding worms of different genetic background with these compounds. Our study is the first step in assigning the relationships of hormonal activity in C. elegans on the substitution at different positions of cholesterol. Wiley-VCH Verlag GmbH & Co. KGaA, 2006.

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