5349-51-9 Usage
Uses
Used in Fragrance Industry:
4-TERT-AMYLCYCLOHEXANOL is used as a fragrance ingredient for its strong, sweet odor, adding pleasant scents to personal care and household products.
Used in Solvent Applications:
4-TERT-AMYLCYCLOHEXANOL is used as a solvent in various chemical processes, leveraging its ability to dissolve other substances effectively.
Used in Chemical Production:
4-TERT-AMYLCYCLOHEXANOL is utilized in the production of other chemicals, contributing to the synthesis of a range of compounds.
Used in Antimicrobial and Anti-Fungal Products:
4-TERT-AMYLCYCLOHEXANOL is used as an antimicrobial and antifungal agent in products designed to inhibit the growth of microorganisms, providing a preservative function and enhancing product safety.
It is crucial to handle 4-TERT-AMYLCYCLOHEXANOL with care due to its potential to cause skin and eye irritation, and it should be used in well-ventilated areas to ensure safety during its application in these various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 5349-51-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,4 and 9 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5349-51:
(6*5)+(5*3)+(4*4)+(3*9)+(2*5)+(1*1)=99
99 % 10 = 9
So 5349-51-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H22O/c1-4-11(2,3)9-5-7-10(12)8-6-9/h9-10,12H,4-8H2,1-3H3
5349-51-9Relevant academic research and scientific papers
ENZYMATIC "IN VITRO" REDUCTION OF KETONES. VI.(1) Reduction rates and stereochemistry of the HLAD-catalyzed reduction of 3-alkyl- and 4-alkylcyclohexanones.
Osselaer, T. A. Van,Lemiere, G. L.,Lepoivre, J. A.,Alderweireldt, F. C.
, p. 133 - 150 (2007/10/02)
Reaction rate constants for the catalytic step HLAD-NADH + ketone * HLAD-NAD+ + alcohol in the HLAD-catalyzed reduction of 3-alkyl- and 4-alkylcyclohexanones are determined from initial rate measurements in the coenzyme recycling system ketone-ethanol-NAD+-HLAD.By rate measurements at several temperatures, activation parameters were determined and isokinetic relationships tracked down.Two different isokinetic relationships show that the 3-alkylcyclohexanones pass through an other type of transition state than cyclohexanone and the 4-alkylcyclohexanones, which means that they have a different arrangement on the HLAD-NADH complex.The results are rationalized in view of the most recent principles on nucleophilic additions to carbonyl functions.The resulting model for the HLAD-catalyzed reduction adequately explains the observed rate accelerating and decelerating effects and the stereochemistry of the reduction as well.
