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81600-07-9

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81600-07-9 Usage

Type of molecule

Triterpene hydrocarbon

Classification

Norhopane

Occurrence

Found in organic matter, such as crude oil

Use

Useful biomarker for the identification and characterization of petroleum compounds

Chemical structure

Polycyclic ring system with 30 carbon atoms

Unique configuration

Alpha hydrogens at the 17th and 21st positions

Potential applications

Petroleum industry, environmental monitoring, and geochemistry
These properties and specific content provide a comprehensive overview of 17ALPHA(H),21ALPHA(H)-30-NORHOPANE, highlighting its importance as a biomarker and its potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 81600-07-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,6,0 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 81600-07:
(7*8)+(6*1)+(5*6)+(4*0)+(3*0)+(2*0)+(1*7)=99
99 % 10 = 9
So 81600-07-9 is a valid CAS Registry Number.

81600-07-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 17ALPHA(H),21ALPHA(H)-30-NORHOPANE

1.2 Other means of identification

Product number -
Other names 3-methyl-5-methylsulfanyl-1H-pyrazolo[4,3-e][1,2,4]triazine

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:81600-07-9 SDS

81600-07-9Downstream Products

81600-07-9Relevant articles and documents

Synthesis of Biological Markers in Fossil Fuels. 1. 17α and 17β Isomers of 30-Norhopane and 30-Normoretane

Bauer, Philip E.,Dunlap, Norma K.,Arseniyadis, Simeon,Watt, David S.,Seifert, Wolfgang K.,Moldowan, J. Michael

, p. 4493 - 4497 (2007/10/02)

21-Hydroxyhopan-3-one was converted to a mixture of 22,29,30-trinor-17α-hopan-21-one and 30-norhopan-22-one by the following reaction sequence: (1) dehydration with phosphorus oxytrichloride, (2) Wolff-Kishner reduction, and (3) ozonolysis.These two keton

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