Welcome to LookChem.com Sign In|Join Free
  • or
2β,3β-Oxido-5α-cholestane is a naturally occurring steroid compound characterized by the presence of an oxygen atom bridging carbons 2 and 3 in the cholestane ring structure. This specific arrangement of atoms and functional groups gives it unique chemical properties and potential biological activities. It is derived from cholesterol and can be found in various biological systems, including plants and animals. The compound plays a role in the metabolism and regulation of cholesterol levels within the body. Due to its structural similarity to cholesterol, 2β,3β-Oxido-5α-cholestane may have implications in the study of cholesterol-related diseases and could be a subject of interest for researchers exploring novel therapeutic approaches.

2789-50-6

Post Buying Request

2789-50-6 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

2789-50-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2789-50-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,8 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2789-50:
(6*2)+(5*7)+(4*8)+(3*9)+(2*5)+(1*0)=116
116 % 10 = 6
So 2789-50-6 is a valid CAS Registry Number.

2789-50-6Upstream product

2789-50-6Relevant academic research and scientific papers

AN ALTERNATIVE ROUTE TO 2α,3α-DIOLS FROM 2,3-UNSATURATED 5α-STEROIDS AVOIDING THE USE OF OSMIUM TETRAOXIDE

Cerny, Vaclav

, p. 2211 - 2217 (2007/10/02)

A method for preparation of 2α,3α-dihydroxy-5α-steroids from 2,3-unsaturated 5α-steroids without the use of OsO4 is described.It involves the sequence of epoxidation, cleavage of the oxirane ring by HI, acetylation, oxidative replacement of iodine by hydroxyl and alkaline hydrolysis (I-IV) without purification of the intermediates.The presence of a 6-keto group does not decrease the yields.The yields are comparable with those obtained by osmylation and the method can find general use, particularly in the synthesis of brassinolide analogs.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 2789-50-6