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1-Methyl-4-[(S)-1,2,3-trimethyl-2-cyclopenten-1-yl]benzene is a complex organic compound with a molecular formula of C16H22. It features a benzene ring with a methyl group at the 1st position and a chiral cyclopentenyl group attached at the 4th position. The cyclopentenyl group is composed of a five-membered ring with three methyl groups and a double bond, with the S-configuration at the chiral center. 1-Methyl-4-[(S)-1,2,3-trimethyl-2-cyclopenten-1-yl]benzene is known for its unique structure and potential applications in various chemical and pharmaceutical industries. Due to its specific arrangement of atoms and functional groups, it may exhibit distinct chemical properties and reactivity compared to its analogs.

4608-39-3

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4608-39-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4608-39-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,0 and 8 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4608-39:
(6*4)+(5*6)+(4*0)+(3*8)+(2*3)+(1*9)=93
93 % 10 = 3
So 4608-39-3 is a valid CAS Registry Number.

4608-39-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (+)-isolaurene

1.2 Other means of identification

Product number -
Other names 1-Methyl-4-((S)-1,2,3-trimethyl-cyclopent-2-enyl)-benzene

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:4608-39-3 SDS

4608-39-3Relevant academic research and scientific papers

Laurencia sesquiterpene biogenetic-type interconversions

Gonzalez,Darias,Martin,Martin,Norte,Perez,Perales,Fayos

, p. 1151 - 1154 (2007/10/02)

Several aromatic sesquiterpenes from Laurencia algae were prepared from chamigrene skeleton precursors. Chemical evidence was adduced to support a biogenetic-type scheme for the synthesis of perforenol and perforene. By means of x ray analysis the structure and absolute configuration of one of the intermediates was established.

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