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3β-chloro-6β-fluoro-5α-cholestan-5α-ol is a complex organic compound belonging to the steroid family, specifically a cholestanol derivative. It features a cholestane core structure with a 5α-hydroxyl group, a 3β-chloro group, and a 6β-fluoro group. This unique combination of functional groups endows the molecule with distinct chemical and biological properties, making it a potential candidate for pharmaceutical applications, particularly in the development of novel drugs targeting cholesterol metabolism and related diseases. The synthesis and study of such compounds can provide valuable insights into the structure-activity relationships within the steroid family, ultimately contributing to the advancement of medical research and drug discovery.

4031-23-6

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4031-23-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4031-23-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,3 and 1 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4031-23:
(6*4)+(5*0)+(4*3)+(3*1)+(2*2)+(1*3)=46
46 % 10 = 6
So 4031-23-6 is a valid CAS Registry Number.

4031-23-6Downstream Products

4031-23-6Relevant academic research and scientific papers

REACTION OF 5,6α-EPOXY-5α-CHOLESTANE AND 5,6α-EPOXY-5α-STIGMASTANE WITH BF3:ETHERATE

Shafiullah,Jamaluddin, Malik

, p. 83 - 86 (2007/10/02)

Reaction of 3β-chloro-5,6α-epoxy-5α-cholestane (1) with BF3:etherate afforded 3β-chloro-5α-cholestan-6-one (3), 3β-chloro-5β,14β-dimethyl-18,19-bisnor-10α-cholest-13(17)-en-6α-ol (4), 3β-chloro-5β-methyl-19-nor-cholest-9(10)-en-6α-ol (5) and 3β-chloro-6β-fluoro-5α-cholestan-5α-ol (6).On similar treatment 3β-acetoxy-5,6α-epoxy-5α-stigmastane (2) gave 3β-acetoxy-5α-stigmastan-6-one (7), 3β-acetoxy-5β,14β-dimethyl-18,19-bisnor-10α-stigmast-13(17)-en-6α-ol (8), 3β-acetoxy-5β-methyl-19-nor-stigmast-9(10)-en-6α-ol (9) and 3β-acetoxy-6β-fluoro-5α-stigmast-5α-ol (10).Compounds 4 and 8 and 5 and 9 were formed via "backbone" and Westphalen rearrangements.The structures of these compounds were established on the basis of spectral data and by comparison with authentic samples.

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