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(4-isopropyl-1-methyl-2-cyclohexenyl) ethyl ether is a complex organic compound with the molecular formula C??H??O. It is a colorless liquid at room temperature and is characterized by its unique chemical structure, which includes a cyclohexene ring with an isopropyl group at position 4, a methyl group at position 1, and an ethyl ether group attached to the cyclohexene ring. (4-isopropyl-1-methyl-2-cyclohexenyl) ethyl ether is known for its aromatic properties and is used in various chemical applications, such as a solvent or a reagent in organic synthesis. Due to its specific structure, it may also have potential applications in the fragrance industry or as a chemical intermediate.

54982-74-0

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54982-74-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54982-74-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,9,8 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 54982-74:
(7*5)+(6*4)+(5*9)+(4*8)+(3*2)+(2*7)+(1*4)=160
160 % 10 = 0
So 54982-74-0 is a valid CAS Registry Number.

54982-74-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-isopropyl-1-methyl-2-cyclohexenyl) ethyl ether

1.2 Other means of identification

Product number -
Other names 1-Ethoxy-1p-menthen

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:54982-74-0 SDS

54982-74-0Downstream Products

54982-74-0Relevant academic research and scientific papers

The reaction of cyclic allylic alcohols with aliphatic alcohols in the presence of cerium(III) chloride

Uzarewicz,Dresler

, p. 181 - 195 (2007/10/03)

Cyclic secondary and tertiary allylic alcohols react with primary aliphatic alcohols in the presence of cerium(III) chloride heptahydrate to give alkyl allylic ethers. When secondary or tertiary aliphatic alcohols are used 1,3-dienes are obtained from allylic alcohols heaving the 3-methyl-2-en-1-ol moiety (3-8, 13-15).

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