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(3-methylcyclohexyl)benzene, with the molecular formula C13H18, is a colorless liquid that is insoluble in water. It possesses a sweet, aromatic odor and is used in various applications due to its unique chemical properties.

17733-69-6

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17733-69-6 Usage

Uses

Used in Fragrance Industry:
(3-methylcyclohexyl)benzene is used as a fragrance ingredient for its sweet, aromatic scent. It is incorporated into the production of perfumes and other scented products to enhance their aroma and appeal to consumers.
Used in Chemical Synthesis:
(3-methylcyclohexyl)benzene serves as an intermediate in the synthesis of other chemicals. Its unique structure allows it to be a valuable component in creating a variety of compounds for different industries.
Used as a Solvent in Industrial Processes:
Due to its solubility properties, (3-methylcyclohexyl)benzene is utilized as a solvent in various industrial processes. It helps dissolve other substances and facilitates chemical reactions in a controlled manner.
Safety Measures:

Check Digit Verification of cas no

The CAS Registry Mumber 17733-69-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,7,3 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17733-69:
(7*1)+(6*7)+(5*7)+(4*3)+(3*3)+(2*6)+(1*9)=126
126 % 10 = 6
So 17733-69-6 is a valid CAS Registry Number.

17733-69-6SDS

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 (3-methylcyclohexyl)benzene

1.2 Other means of identification

Product number -
Other names 1-methyl-3-phenylcyclohexanecarboxylic acid

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:17733-69-6 SDS

17733-69-6Relevant academic research and scientific papers

ALKYLATION OF BENZENE WITH 4-METHYLCYCLOHEXANOL IN THE PRESENCE OF SULFURIC ACID

Lipovich, V. G.,Zemskov, V. V.,Ratovskii, G. V.,Burlakova, O. V.

, p. 109 - 112 (2007/10/02)

Alkylation of benzene with 4-methylcyclohexanol in the presence of methylcyclohexane and 96, 88, and 80percent H2SO4 has been studied.It was established that depending on the solubility of the starting components in sulfuric acid, alkylation occurs in the inorganic phase or on the interface between the organic and inorganic phases.The yield and composition of the catalysate are determined to a significant degree by the extent of the alkylation process and intramolecular hydride transfers.

REACTION OF 1-CHLORO-1-METHYLCYCLOHEXANE WITH PHENYL- AND BENZYL- TRIMETHYLSILANES IN THE PRESENCE OF ALUMINIUM CHLORIDE

Bolestova, G. I.,Parnes, Z. N.,Vol'pin, M. E.

, p. 967 - 971 (2007/10/02)

In the reaction of 1-chloro-1-methylcyclohexane with phenyltrimethylsilane and benzyltrimethylsilane in the presence of aluminum chloride the chlorine atom is substituted by a phenyl or benzyl group with the formation of 1-methyl-1-phenyl- and 1-methyl-1-benzylcyclohexane, respectively.In the case of benzyltrimethylsilane the products from alkylation of the benzene ring of the benzyltrimethylsilane by the 1-methylcyclohexyl carbocation in the Friedel-Crafts reaction are formed in addition to 1-methyl-1-benzylcyclohexane.

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