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2,5-Cyclohexadien-1-ol,1-methyl-4-(1-methylethyl)-,trans-(9CI) is a cyclic alcohol chemical compound with the molecular formula C10H14O. It features a cyclohexene ring with a methyl and isopropyl group attached, existing in a trans configuration. Known for its pleasant aroma, 2,5-Cyclohexadien-1-ol,1-methyl-4-(1-methylethyl)-,trans-(9CI) is utilized in various applications, including the synthesis of organic compounds and as a flavoring agent in the food industry. Due to its flammable nature, it requires careful handling to mitigate potential hazards.

103974-35-2

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103974-35-2 Usage

Uses

Used in Organic Synthesis:
2,5-Cyclohexadien-1-ol,1-methyl-4-(1-methylethyl)-,trans-(9CI) is used as a key intermediate in the synthesis of various organic compounds. Its unique structure allows for versatile chemical reactions, making it a valuable component in the creation of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Flavoring Agents for the Food Industry:
Leveraging its pleasant aroma, 2,5-Cyclohexadien-1-ol,1-methyl-4-(1-methylethyl)-,trans-(9CI) is employed as a flavoring agent in the food industry. It enhances the taste and smell of various food products, contributing to a more enjoyable consumer experience.
Used in Fragrance Industry:
2,5-Cyclohexadien-1-ol,1-methyl-4-(1-methylethyl)-,trans-(9CI)'s appealing scent also makes it suitable for use in the fragrance industry, where it can be incorporated into perfumes, colognes, and other scented products to provide a distinct and attractive aroma.
Used in Research and Development:
2,5-Cyclohexadien-1-ol,1-methyl-4-(1-methylethyl)-,trans-(9CI) is utilized in research and development settings for studying its chemical properties and potential applications. Scientists and researchers explore its reactivity, stability, and interactions with other compounds to discover new uses and improve existing processes.
Safety Considerations:
Due to its flammable nature, 2,5-Cyclohexadien-1-ol,1-methyl-4-(1-methylethyl)-,trans-(9CI) should be handled with care to prevent accidents and ensure the safety of individuals working with the compound. Proper storage, handling, and disposal protocols must be followed to minimize risks associated with its hazardous properties.

Check Digit Verification of cas no

The CAS Registry Mumber 103974-35-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,9,7 and 4 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 103974-35:
(8*1)+(7*0)+(6*3)+(5*9)+(4*7)+(3*4)+(2*3)+(1*5)=122
122 % 10 = 2
So 103974-35-2 is a valid CAS Registry Number.

103974-35-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-Cyclohexadien-1-ol,1-methyl-4-(1-methylethyl)-,trans-(9CI)

1.2 Other means of identification

Product number -
Other names -

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

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More Details:103974-35-2 SDS

103974-35-2Relevant academic research and scientific papers

PHOTO-OXIDATION OF α-PHELLANDRENE: THE FORMATION OF CYCLOHEXADIENYL HYDROPEROXIDES AND THEIR REDUCTION TO ARENE 1,4-HYDRATES

Atkins, Robert,Carless, Howard A. J.

, p. 6093 - 6096 (2007/10/02)

Dye-sensitised photo-oxidation of α-phellandrene (3) yields, besides the expected endoperoxides, the cyclohexadienyl hydroperoxides (6) and (7) reduction of these latter gives the unstable arene 1,4-hydrates (9) and (10).

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