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2β,3β,14-Trihydroxy-5α-cholest-7-en-6-one, also known as 7-ketolithocholic acid, is a naturally occurring bile acid derived from the metabolism of cholesterol. It is a steroid compound with a unique structure characterized by the presence of three hydroxyl groups at the 2β, 3β, and 14 positions, and a ketone group at the 6 position. This molecule plays a crucial role in the digestion and absorption of dietary fats and fat-soluble vitamins in the human body. Additionally, it has been implicated in various physiological processes, such as cholesterol homeostasis and bile acid signaling. Due to its potential impact on human health, research on 2β,3β,14-trihydroxy-5α-cholest-7-en-6-one has been conducted to better understand its role in various biological pathways and its potential therapeutic applications.

7698-67-1

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7698-67-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7698-67-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,9 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7698-67:
(6*7)+(5*6)+(4*9)+(3*8)+(2*6)+(1*7)=151
151 % 10 = 1
So 7698-67-1 is a valid CAS Registry Number.

7698-67-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5α-22,25-dideoxy-ecdysone

1.2 Other means of identification

Product number -
Other names 5α-22,25-dideoxyecdysone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7698-67-1 SDS

7698-67-1Downstream Products

7698-67-1Relevant academic research and scientific papers

Novel synthesis of 22,25-dideoxyecdysone and its 5α-isomer

Kovganko,Survilo

, p. 340 - 343 (2002)

22,25-Dideoxyecdysone (1) and 5α-22,25-dideoxyecdysone (1a) were prepared from cholesterol via a new scheme using the key intermediates 3β-chloro-5α-bromo-6-ketone 3, 3β-chloro-7α -bromo-6-ketone 4, and 2,7-dien-6-one 7.

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