32296-45-0 Usage
Clear, colorless liquid
The compound appears as a transparent and colorless liquid, which is a characteristic of its physical state.
Mild floral odor
1-Ethyl-2-methylcyclohexanol has a subtle and pleasant floral scent, which contributes to its use as a fragrance ingredient.
Fragrance ingredient
It is commonly used in perfumes and personal care products due to its appealing scent.
Industrial solvent
The compound serves as a solvent in various industrial applications, taking advantage of its properties.
Produced through hydrogenation
1-Ethyl-2-methylcyclohexanol is synthesized by hydrogenating the corresponding cyclic ketone.
Low volatility
The compound has a low tendency to vaporize, making it suitable for long-lasting scent in formulations.
High boiling point
The high boiling point of 1-Ethyl-2-methylcyclohexanol allows it to be used as a solvent for non-volatile substances.
Potential irritant
This chemical may have irritant properties, so it's important to handle it with care.
Ventilation requirement
To minimize potential irritation or health risks, 1-Ethyl-2-methylcyclohexanol should be used in well-ventilated areas.
Check Digit Verification of cas no
The CAS Registry Mumber 32296-45-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,2,9 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 32296-45:
(7*3)+(6*2)+(5*2)+(4*9)+(3*6)+(2*4)+(1*5)=110
110 % 10 = 0
So 32296-45-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H18O/c1-3-9(10)7-5-4-6-8(9)2/h8,10H,3-7H2,1-2H3
32296-45-0Relevant articles and documents
Stereochemical Investigations of Samarium(II) Iodide-Promoted 5-Exo and 6-Exo Ketyl-Olefin Radical Cyclization Reactions
Molander, Gary A.,McKie, Jeffrey A.
, p. 872 - 882 (2007/10/02)
Samarium(II) iodide (SmI2)-promoted ketyl cyclizations of several substituted, unsaturated ketones, providing various cyclpentyl and cyclohexyl systems, have been investigated.The resulting experiments provide stereochemical insight into these reactions and in addition outline the synthetic potential of these 5-exo and 6-exo radical cyclization processes.
