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(4-Propylcyclohexyl)benzene is an organic compound that falls under the category of aromatic hydrocarbons. It features a distinctive structure with a six-membered cyclohexyl ring to which a propyl group (a three-carbon chain) is attached at the 4th position. This cyclohexyl ring is then connected to a benzene ring through a single bond, endowing it with particular physical and chemical characteristics. As a specialty chemical, it is primarily utilized in research and scientific experimentation.

177533-41-4

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177533-41-4 Usage

Uses

Used in Research and Scientific Experimentation:
(4-Propylcyclohexyl)benzene is used as a research chemical for [application reason], given its unique structure and properties. It is predominantly employed in the field of organic chemistry to study the effects of its specific molecular arrangement on various chemical reactions and interactions.
Used in Organic Chemistry:
(4-Propylcyclohexyl)benzene is used as a model compound for [application reason], allowing researchers to investigate the influence of its cyclohexyl ring and propyl group on the reactivity and stability of aromatic hydrocarbons. This can provide insights into the design of new molecules with tailored properties for specific applications.

Check Digit Verification of cas no

The CAS Registry Mumber 177533-41-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,7,5,3 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 177533-41:
(8*1)+(7*7)+(6*7)+(5*5)+(4*3)+(3*3)+(2*4)+(1*1)=154
154 % 10 = 4
So 177533-41-4 is a valid CAS Registry Number.

177533-41-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-Propylcyclohexyl)benzene

1.2 Other means of identification

Product number -
Other names trans-4-propylcyclohexylbenzene

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:177533-41-4 SDS

177533-41-4Relevant academic research and scientific papers

Liquid crystal compound having negative dielectric anisotropy, and liquid crystal composition

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, (2015/11/10)

A liquid crystal composition includes a liquid crystal compound having a formula (I), where R1 and R2 are independently selected from the group consisting of H, C1-C10 alkyl, C2-C10 alkenyl, C1-C10 alkoxyl, C2-C10 alkenyloxy, C1-C10 ether, C1-C10 aldehyde, C1-C10 ketone, and C1-C10 ester; A is selected from the group consisting of and X1, X2, X3 and X4 are independently selected from the group consisting of H, halogen group, —CF3, —CHF2, —CH2F, —OCF3, —OCHF2 and —OCH2F, at least one of X1, X2, X3 and X4 being halogen group, —CF3, —CHF2, —CH2F, —OCF3, —OCHF2 or —OCH2F.

4-(4-ALKYLCYCLOHEXYL)BENZALDEHYDE

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Page/Page column 10-11, (2009/02/10)

A process for effectively producing a 4-(4-alkylcyclohexyl)benzaldehyde, 4-(cyclohexyl)benzaldehyde, a 4-(trans-4-alkylcyclohexyl)benzaldehyde and a (trans-4-alkylcyclohexyl)benzene useful for electronic material applications such as liquid crystals and for pharmaceutical and agrochemical applications, etc., are disclosed. The present invention provides (1) a process for producing a 4-(4-alkylcyclohexyl)benzaldehyde or 4-(cyclohexyl)benzaldehyde by formylating a (4-alkylcyclohexyl)benzene or cyclohexylbenzene with carbon monoxide, (2) a process for producing a 4-(trans-4-alkylcyclohexyl)benzaldehyde by formylating a (4-alkylcyclohexyl)benzene having a cis/trans molar ratio of 0.3 or less with carbon monoxide, and (3) a process for producing a (trans-4-alkylcyclohexyl)benzene by isomerizing a mixture of the cis and trans isomers of a (4-alkylcyclohexyl)benzene, all of the processes being performed in the presence of HF and BF3.

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