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Benzene, 1-cyclohexyl-4-(1-methylethyl)-, also known as 1-cyclohexyl-4-isopropylbenzene, is an organic compound with the chemical formula C??H??. It is a derivative of benzene, featuring a cyclohexyl group attached to the 1-position and an isopropyl group (1-methylethyl) at the 4-position. Benzene, 1-cyclohexyl-4-(1-methylethyl)- is a colorless liquid with a distinct aromatic odor and is used in various chemical syntheses, particularly in the production of pharmaceuticals and agrochemicals. It is also an intermediate in the synthesis of certain polymers and dyes. Due to its complex structure and potential applications, it is important to handle this chemical with care, adhering to proper safety protocols.

4501-42-2

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4501-42-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4501-42-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,0 and 1 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4501-42:
(6*4)+(5*5)+(4*0)+(3*1)+(2*4)+(1*2)=62
62 % 10 = 2
So 4501-42-2 is a valid CAS Registry Number.

4501-42-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-cyclohexyl-4-isopropylbenzene

1.2 Other means of identification

Product number -
Other names 1-Cyclohexyl-4-isopropyl-benzol

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:4501-42-2 SDS

4501-42-2Relevant academic research and scientific papers

Design of Bowl-Shaped N-Hydroxyimide Derivatives as New Organoradical Catalysts for Site-Selective C(sp3)?H Bond Functionalization Reactions

Kato, Terumasa,Maruoka, Keiji

supporting information, p. 14261 - 14264 (2020/07/13)

A series of new bowl-shaped N-hydroxyimide derivatives has been designed and used as selective organoradical catalysts. A number of these bowl-shaped N-hydroxyimide derivatives exhibit excellent site-selectivity in the amination of benzylic C(sp3)?H bonds in aromatic hydrocarbon substrates.

Iron-catalyzed arene alkylation reactions with unactivated secondary alcohols

Jefferies, Latisha R.,Cook, Silas P.

supporting information, p. 2026 - 2029 (2014/05/06)

A simple, iron-based catalytic system allows for the inter- and intramolecular arylation of unactivated secondary alcohols. This transformation expands the substrate scope beyond the previously required activated alcohols and proceeds under mild reaction conditions, tolerating air and moisture. Furthermore, the use of an enantioenriched secondary alcohol provides an enantioenriched product for the intramolecular reaction, thereby offering a convenient approach to nonracemic products.

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