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63543-60-2

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63543-60-2 Usage

Type

Trinorhopane derivative

Structure

Triterpenoid structure

Composition

Hydrocarbon composed of carbon and hydrogen atoms

Occurrence

Found in natural sources such as plants and certain petroleum derivatives

Applications

Pharmaceutical and chemical industries

Potential Biological Activities

May exhibit biological activities and properties

Interest for Research and Development

Subject of interest for further research and development

Study Fields

Organic chemistry
Pharmacology
Medicinal chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 63543-60-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,5,4 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 63543-60:
(7*6)+(6*3)+(5*5)+(4*4)+(3*3)+(2*6)+(1*0)=122
122 % 10 = 2
So 63543-60-2 is a valid CAS Registry Number.
InChI:InChI=1/C27H44/c1-23(2)13-8-15-25(4)21(23)12-16-27(6)22(25)11-10-20-19-9-7-14-24(19,3)17-18-26(20,27)5/h21-22H,7-18H2,1-6H3/t21-,22+,24-,25-,26+,27+/m0/s1

63543-60-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (3aS,5aS,5bR,7aS,11aS,11bR)-3a,5a,5b,8,8,11a-hexamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13-tetradecahydrocyclopenta[a]chrysene

1.2 Other means of identification

Product number -
Other names 17|A-20,29,30-Trinorlup-13(18)-ene

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:63543-60-2 SDS

63543-60-2Downstream Products

63543-60-2Relevant articles and documents

Synthesis of Biological Markers in Fossil Fuels. 3. Degraded and Rearranged C27 Hopanes

Dunlap, Norma K.,Sabol, Mark R.,Bauer, Philip E.,Watt, David S.,Reibenspies, Joseph H.,et al.

, p. 1826 - 1829 (2007/10/02)

22-Hydroxyhopan-3-one was converted to various C27 hopane hydrocarbons: 22,29,30-trinorhopane, 22,29,30-trinor-17α-hopane, 22,29,30-trinor-28(18 -> 17S)abeo-13α,18β-hopane, and 22,29,30-trinor-28(18 -> 17S)abeo-13α,18α-hopane.These hydrocarbons are useful as biological markers in studies related to the source, maturation, and migration of crude oils.

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