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11B-HYDROXYETIOCHOLANOLONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

739-26-4

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739-26-4 Usage

Uses

A metabolite of Etiocholanolone.

Check Digit Verification of cas no

The CAS Registry Mumber 739-26-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,3 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 739-26:
(5*7)+(4*3)+(3*9)+(2*2)+(1*6)=84
84 % 10 = 4
So 739-26-4 is a valid CAS Registry Number.
InChI:InChI=1/C19H30O3/c1-18-8-7-12(20)9-11(18)3-4-13-14-5-6-16(22)19(14,2)10-15(21)17(13)18/h11-15,17,20-21H,3-10H2,1-2H3/t11-,12-,13+,14+,15+,17-,18+,19+/m1/s1

739-26-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (3R,5R,8S,9S,10S,11S,13S,14S)-3,11-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,14,15,16-tetradecahydrocyclopenta[a]phenanthren-17-one

1.2 Other means of identification

Product number -
Other names 5BETA-ANDROSTANE-3BETA,11BETA-DIOL-17-ONE

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:739-26-4 SDS

739-26-4Relevant academic research and scientific papers

NEUROACTIVE STEROIDS, COMPOSITIONS, AND USES THEREOF

-

Page/Page column 87; 88, (2015/02/02)

Described herein are neuroactive steroids of the Formula (I): (Formula (I)) or a pharmaceutically acceptable salt thereof; wherein R1a and R1b are as defined herein. Such compounds are envisioned, in certain embodiments, to behave as GABA modulators. The present invention also provides pharmaceutical compositions comprising a compound of the present invention and methods of use and treatment, e.g., such for inducing sedation and/or anesthesia.

METHODS FOR THE PURIFICATION OF DEOXYCHOLIC ACID

-

, (2013/06/05)

Synthetic methods for preparing deoxycholic acid and intermediates thereof, high purity synthetic deoxycholic acid, compositions and methods of use are provided. Also, provided are processes for the synthesis of 12-keto or 12-α-hydroxy-steroids from Δ-9,11-ene, 11-keto or 11-hydroxy-β-steroids. This invention is also directed to novel compounds prepared during the synthesis. This invention is also directed to the synthesis of deoxycholic acid starting from hydrocortisone.

METHODS FOR THE PURIFICATION OF DEOXYCHOLIC ACID

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Page/Page column 68, (2011/07/07)

Synthetic methods for preparing deoxycholic acid and intermediates thereof, high purity synthetic deoxycholic acid, compositions and methods of use are provided. Also, provided are processes for the synthesis of 12-keto or 12-α-hydroxysteroids from Δ-9,11-ene, 11-keto or 11-hydroxy-β-steroids. This invention is also directed to novel compounds prepared during the synthesis. This invention is also directed to the synthesis of deoxycholic acid starting from hydrocortisone.

SYNTHESIS OF 11-HYDROXYLATED ANDROSTANE DERIVATIVES

Fajkos, Jan,Joska, Jiri

, p. 1845 - 1849 (2007/10/02)

Reaction conditions for selective reductions of 3- and 17-oxo groups are described and applied to syntheses of 11-hydroxylated derivatives.

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