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(10α)-B-Nor-1-oxo-5,6-secocholest-2-en-6-oic acid is a complex organic compound with the molecular formula C27H40O3. It is a derivative of cholesterol, featuring a modified steroid structure with a norbornane ring and a secocholestane skeleton. This molecule is characterized by the presence of a ketone group at the 1-position, a double bond between carbons 5 and 6, and a carboxylic acid group at the 6-position. It is an example of a triterpenoid, which are a class of naturally occurring organic compounds derived from the isoprene rule. Triterpenoids are known for their diverse biological activities and are found in various plants, fungi, and insects. The specific structure of (10α)-B-Nor-1-oxo-5,6-secocholest-2-en-6-oic acid suggests it may have potential applications in pharmaceutical or chemical research, although its exact properties and uses would require further investigation.

3949-50-6

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3949-50-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3949-50-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,4 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3949-50:
(6*3)+(5*9)+(4*4)+(3*9)+(2*5)+(1*0)=116
116 % 10 = 6
So 3949-50-6 is a valid CAS Registry Number.

3949-50-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,7-Seco-6-nor-cholesten-(3)-on-(5)-carbonsaeure-(7)

1.2 Other means of identification

Product number -
Other names 5-Keto-5,7-seco-6-nor-cholesten-(3)-carbonsaeure-(7)

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:3949-50-6 SDS

3949-50-6Relevant academic research and scientific papers

BAEYER-VILLIGER OXIDATION OF 3-β-CHLOROCHOLEST-5-EN-7-ONE

Shafiullah,Khan, E. A.

, p. 329 - 332 (2007/10/02)

Oxidation of 3β-chlorocholest-5-en-7-one (1) with perbenzoic acid (1 or 2 mole equivalents) in the presence of p-toluenesulfonic acid monohydrate as catalyst afforded 3β-chloro-5,6-α-oxido-5α-cholestan-7-one (2), 3β-chloro-7a-oxa-B-homocholest-5-en-7-one (3), 3β-chloro-5-formyl-6-oxa-5α-cholestan-7-one (4) and 3β-chloro-5-oxo-5,7-seco-6-norcholestan-7-oic acid (5).With 3 mole equivalents, 1 provided, in addition to 2-5, 5-oxo-5,7-seco-6-norcholest-3-en-7-oic acid (6).The seco-acids 5 and 6 were converted to the methyl esters (7) and (8).The structures of the compounds have been established on the basis of their spectral properties, chemical transformations and comparison with authentic samples.

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