68039-42-9 Usage
Uses
Used in Flavor and Fragrance Industry:
4-(1,1-dimethylethyl)cyclohexyl formate is used as a flavoring agent for its fruity scent and taste, enhancing the sensory experience of various food products. Its ability to impart a pleasant aroma makes it a sought-after ingredient in the creation of perfumes and fragrances.
Used in Organic Synthesis:
In the field of organic chemistry, 4-(1,1-dimethylethyl)cyclohexyl formate serves as a key intermediate in the synthesis of a range of organic compounds. Its reactivity and functional groups contribute to the development of new molecules with potential applications in various industries.
Used in Food Industry:
4-(1,1-dimethylethyl)cyclohexyl formate is used as a flavor enhancer in the food industry, adding depth and complexity to the taste profiles of various products. Its fruity notes can complement a wide array of food items, from beverages to confectionery.
Used in Perfume and Fragrance Industry:
In the perfume and fragrance industry, 4-(1,1-dimethylethyl)cyclohexyl formate is used to create captivating scents. Its fruity aroma can be blended with other ingredients to produce unique and appealing fragrances for personal care products and home fragrances.
Safety Considerations:
While 4-(1,1-dimethylethyl)cyclohexyl formate offers numerous applications, it is essential to handle it with care due to its potential irritant and toxic properties. Proper safety measures should be implemented during its production, storage, and use to minimize risks to human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 68039-42-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,0,3 and 9 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 68039-42:
(7*6)+(6*8)+(5*0)+(4*3)+(3*9)+(2*4)+(1*2)=139
139 % 10 = 9
So 68039-42-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H20O2/c1-11(2,3)9-4-6-10(7-5-9)13-8-12/h8-10H,4-7H2,1-3H3
68039-42-9Relevant academic research and scientific papers
Dual behavior of alcohols in iodine-catalyzed esterification under solvent-free reaction conditions
Jereb, Marjan,Vra?i?, Dejan,Zupan, Marko
body text, p. 2347 - 2352 (2009/09/06)
The dual behavior phenomenon of alcohols in iodine-catalyzed esterification under solvent-free reaction conditions (SFRCs) is described; the governing factor is the stability of the carbonium ion generated from the alcohol; high concentration reaction conditions (HCRCs) or dilute solutions are much less suitable. In the case of benzylic alcohols, loss of optical activity was noted, whereas alkyl alcohols furnished a product with retention of stereochemistry.
One-step conversion of formate esters to O-silyl ethers by means of samarium diiodide in the presence of chlorosilane reagents
Honda, Toshio,Ishikawa, Fumihiro
, p. 3323 - 3328 (2007/10/03)
One-step conversion of various types of formate esters into the corresponding O-silyl ethers under neutral reaction conditions was established by employing samarium diiodide in the presence of chlorosilane reagents.
Efficient catalytic reduction of ketones with formic acid and ruthenium complexes
Menashe, Naim,Salant, Einat,Shvo, Youval
, p. 97 - 102 (2007/10/03)
The ruthenium complex (η5-C4Ph4COHOC4Ph4-η5)( μ-H)(CO)4Ru2 and its phenyl ring-substituted derivatives were found to act as efficient catalysts in reduction reactions of aldehydes and ketones to alcohols, using formic acid as H source. Excess formic acid accelerates the reaction, and the corresponding formate esters were isolated as sole products. Turnover numbers of up to 8000 (alcohols) and 11000 (formate esters) were attained, with yields in the order of 90%. Alkenes are not reactive, however, double bonds conjugated to a carbonyl group are selectively reduced under the reaction conditions. The reaction is compatible with a variety of ketones, but with aliphatic aldehydes the reaction is not selective, inasmuch as aldol condensation products are formed.
