24348-06-9 Usage
Description
[1R-(1α,4β,6α)]-4-hydroxy-4,7,7-trimethylbicyclo[4.1.0]heptan-3-one is a bicyclic ketone chemical compound characterized by its complex molecular structure, featuring a hydroxyl group and three methyl substituents. [1R-(1alpha,4beta,6alpha)]-4-hydroxy-4,7,7-trimethylbicyclo[4.1.0]heptan-3-one is known for its rigid and compact structure due to the presence of the bicyclo[4.1.0]heptane framework.
Uses
Used in Fragrance Industry:
[1R-(1α,4β,6α)]-4-hydroxy-4,7,7-trimethylbicyclo[4.1.0]heptan-3-one is used as a fragrance ingredient for its pleasant, woody odor. It is commonly utilized in the production of perfumes, colognes, and other scented products, contributing to their overall aroma.
Used in Flavor Industry:
In the flavor industry, [1R-(1α,4β,6α)]-4-hydroxy-4,7,7-trimethylbicyclo[4.1.0]heptan-3-one is used as a flavoring agent. It is added to various food and beverage products to enhance their aroma and taste, providing a unique and desirable sensory experience for consumers.
Used in Cosmetic Industry:
[1R-(1α,4β,6α)]-4-hydroxy-4,7,7-trimethylbicyclo[4.1.0]heptan-3-one is also employed in the cosmetic industry, where it serves as a key ingredient in the formulation of scented products such as lotions, creams, and other personal care items. Its woody odor adds a pleasant and appealing fragrance to these products, making them more attractive to consumers.
Check Digit Verification of cas no
The CAS Registry Mumber 24348-06-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,3,4 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 24348-06:
(7*2)+(6*4)+(5*3)+(4*4)+(3*8)+(2*0)+(1*6)=99
99 % 10 = 9
So 24348-06-9 is a valid CAS Registry Number.
24348-06-9Relevant articles and documents
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Carson,M.S. et al.
, p. 2220 - 2223 (1969)
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SYNTHESIS OF METHYL 1R-CIS-2,2-DIMETHYL-3-(2-OXOPROPYL)CYCLOPROPANECARBOXYLATE, AN INTERMEDIATE FOR SYNTHETIC PYRETHROIDS
Muljiani, Z.,Deshmukh, A. R. A. S.,Gadre, S. R.,Joshi, V. S.
, p. 25 - 32 (2007/10/02)
Synthesis of keto ester (1) from (+)-3-carene is described.Ring cleavage is effected by the Beckmann Fragmentation.
STEREOCHEMISTRY OF THE CARANE SYSTEM. OXIDATION PRODUCTS OF ISOMERIC 3,4-CARANEDIOLS OBTAINED FROM (+)-3-CARENE
Hendrich, Aleksandra,Piatkowski, Krzysztof
, p. 73 - 84 (2007/10/02)
Oxidation of four isomeric 3,4-caranediols has been carried out and reaction products have been investigated.It has been found that cis-diols rather form cyclic ketals than are oxidized under conditions of the Jones reaction.The key intermediate for syntheses of chrysanthemic acid, (-)-2-acetonyl-3,3-dimethylcyclopropaneacetic acid was obtained exclusively by oxidation of (-)-3β,4α-caranediol.