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4-methoxy-2-methyl-1-(propan-2-yl)benzene is an organic compound with the molecular formula C11H16O. It is a derivative of benzene, featuring a methyl group at the 2nd carbon, a propyl group at the 1st carbon, and a methoxy group at the 4th carbon. This aromatic compound is characterized by its unique structure, which contributes to its distinct chemical properties and potential applications in various fields, such as pharmaceuticals and fragrances. The compound's molecular structure and functional groups make it an interesting target for synthetic chemistry and material science research.

5436-42-0

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5436-42-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5436-42-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,3 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5436-42:
(6*5)+(5*4)+(4*3)+(3*6)+(2*4)+(1*2)=90
90 % 10 = 0
So 5436-42-0 is a valid CAS Registry Number.

5436-42-0SDS

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 4-methoxy-2-methyl-1-propan-2-ylbenzene

1.2 Other means of identification

Product number -
Other names p-Thymol-methylaether

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:5436-42-0 SDS

5436-42-0Relevant academic research and scientific papers

Total Syntheses of Crinipellins Enabled by Cobalt-Mediated and Palladium-Catalyzed Intramolecular Pauson–Khand Reactions

Huang, Zhihui,Huang, Jun,Qu, Yongzheng,Zhang, Weibin,Gong, Jianxian,Yang, Zhen

supporting information, p. 8744 - 8748 (2018/07/14)

Efficient total syntheses of the naturally occurring, potent antibiotic compounds (?)-crinipellin A and (?)-crinipellin B are described. The key advanced intermediate, a fully functionalized tetraquinane core, was constructed by a novel thiourea/palladium-catalyzed Pauson–Khand reaction. This intermediate can serve as a common intermediate for the collective total synthesis of other members of the crinipellin family.

THE CLEMMENSEN REDUCTION OF ENOL ETHERS: CYCLOPROPYL ETHERS FROM MONO- AND DI-METHOXYCYCLOHEXA-1,4-DIENES

Elphimoff-Felkin, Irene,Sarda, Pierre

, p. 4425 - 4428 (2007/10/02)

Clemmensen reduction (zinc and hydrogen chloride in dry diethyl ether) of 1-methoxy- and 1,5-dimethoxy-cyclohexa-1,4-diene affords the cyclopropyl ethers, 1-methoxy- and 1,5-dimethoxy-bicyclohexane; in the presence of acetic anhydride, reduction of 6-acetyl-1-methoxy-6-methyl-cyclohexa-1,4-diene leads regiospecifically to 7-acetoxy-1-methoxy-6,7-dimethyl-bicyclohept-4-ene.

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