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82079-08-1

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82079-08-1 Usage

Natural Occurrence

Found in certain animal tissues and plant oils.

Cholestene Derivative

Belongs to a group of compounds derived from cholesterol.

Specific Isomer

Unique arrangement of atoms and functional groups within its structure.

Biological Activities

Known for its potential anti-inflammatory and immunomodulatory effects.

Drug Development Potential

Suggests possible applications in the field of drug development.

Precursor for Synthesis

Serves as a precursor for the synthesis of other bioactive compounds.

Therapeutic Significance

Possesses potential therapeutic applications.

Industrial Importance

Has potential industrial applications and significance.

Check Digit Verification of cas no

The CAS Registry Mumber 82079-08-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,0,7 and 9 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 82079-08:
(7*8)+(6*2)+(5*0)+(4*7)+(3*9)+(2*0)+(1*8)=131
131 % 10 = 1
So 82079-08-1 is a valid CAS Registry Number.

82079-08-1SDS

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 20R 13(17)-DIACHOLESTENE

1.2 Other means of identification

Product number -
Other names 20-(4-Octylphenoxy)-3,6,9,12,15,18-hexaoxaicosan-1-ol

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:82079-08-1 SDS

82079-08-1Downstream Products

82079-08-1Relevant articles and documents

Synthesis of Biological Markers in Fossil Fuels. 4. C27, C28, and C29 13β,17α(H)-Diasteranes

Bauer, Phillip E.,Nelson, David A.,Watt, David S.,Reibenspies, Joseph H.,Anderson, Oren P.,et al.

, p. 5460 - 5464 (2007/10/02)

The rearrangement of 5-cholestene to (20ξ)-13(17)-diacholestenes, separation of C-20 epimers, and further reduction provided an unambiguous synthesis of the biomarkers (20R)- and (20S)-13β,17α(H)-diacholestanes.Repetition of this sequence using (24R)-5-campestene or (24R)-5-stigmastene provided the analogous C28 and C29 diasteranes.

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