26252-11-9 Usage
Uses
Used in the Food and Beverage Industry:
4-(isopropyl)-1-methylcyclohexyl acetate is used as a flavoring agent for its ability to impart a subtle fruity note to food and beverages, thereby enriching their taste profiles and consumer appeal.
Used in Personal Care Products:
In the personal care industry, 4-(isopropyl)-1-methylcyclohexyl acetate is utilized as a fragrance component in perfumes and cosmetics. Its mild and fruity scent adds a pleasant olfactory dimension to these products, contributing to their overall sensory appeal.
Safety Considerations:
While 4-(isopropyl)-1-methylcyclohexyl acetate is widely used in consumer goods, it is important to handle it with care due to its potential to cause irritation to the eyes, skin, and respiratory system if exposure occurs at high concentrations. Proper safety measures should be taken during its production, use, and disposal to mitigate any adverse effects.
Check Digit Verification of cas no
The CAS Registry Mumber 26252-11-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,2,5 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 26252-11:
(7*2)+(6*6)+(5*2)+(4*5)+(3*2)+(2*1)+(1*1)=89
89 % 10 = 9
So 26252-11-9 is a valid CAS Registry Number.
26252-11-9Relevant academic research and scientific papers
SOLVOLYTIC DISPLACEMENT OF ALKYL HALIDES BY METAL SALTS. PREPARATIVE PROCEDURES FOR ALLYL-, BENZYL- AND TERTIARY ALKYL-OXY DERIVATIVES USING THE ZINC SALTS
Gurudutt, K. N.,Ravindranath, B.,Srinivas, P.
, p. 1843 - 1846 (2007/10/02)
Reaction of allylic, benzylic and tertiary alkyl halides with zinc oxide in protic solvents leads to the formation of the corresponding alcohols, ethers and esters in good yields.The scope and limitations of this reaction have been examined.The possible involvement of ion quadruplets in the reaction is suggested.
Zinc salt assisted solvolyses of tertiary alkyl halides
Anandaraman,Gurudutt,Natarajan,Ravindranath
, p. 2189 - 2190 (2007/10/02)
Tertiary alkyl halides undergo facile substitution reactions under solvolytic conditions in presence of zinc ions yielding alcohols, ethers and esters.
