84559-99-9 Usage
Description
3,5,5-Trimethylcyclohex-2-ene-1-carbaldehyde is a chemical compound with the molecular formula C10H16O. It is a colorless to pale yellow liquid with a strong, fruity odor. The chemical structure of 3,5,5-trimethylcyclohex-2-ene-1-carbaldehyde contains a cyclohexene ring with three methyl groups and an aldehyde functional group, which gives it its distinct odor and reactivity.
Uses
Used in Fragrance Industry:
3,5,5-Trimethylcyclohex-2-ene-1-carbaldehyde is used as a fragrance ingredient for its strong, fruity odor. It is incorporated into various consumer products such as perfumes, soaps, and lotions to provide a pleasant and long-lasting scent.
Used in Organic Synthesis:
3,5,5-Trimethylcyclohex-2-ene-1-carbaldehyde is also used in the synthesis of other organic compounds. Its reactive aldehyde functional group allows it to participate in various chemical reactions, making it a valuable building block for the creation of new molecules in the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 84559-99-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,5,5 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 84559-99:
(7*8)+(6*4)+(5*5)+(4*5)+(3*9)+(2*9)+(1*9)=179
179 % 10 = 9
So 84559-99-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H16O/c1-8-4-9(7-11)6-10(2,3)5-8/h4,7,9H,5-6H2,1-3H3
84559-99-9Relevant articles and documents
Structure-odor correlation, XXIV: Synthesis and olfactory properties of damascene and damascenone analogs
Weyerstahl, Peter,Licha, Kai
, p. 809 - 814 (2007/10/03)
The aldehydes rac-1, rac-2, and 3 were conveniently prepared by starting from isophorone (4). Reaction of 1-3 with (E,Z)-1-bromo-1-propene (14) afforded the rac-allylic alcohols (E,Z)-15, -18, and -20. The alcohols were oxidized to the damascone/damascenone analogs 1-(3,5,5-trimethyl-2-cyclohexen-1-yl)- (rac-16), 1-(3,5,5-trimethyl-1-cyclohexen-1-yl)-(rac-19), and 1-(3,5,5-trimethyl-1,3-cyclohexadien-1-yl)-2-buten-1-one (21), and the (E/Z) isomers were separated by FC. Their olfactory evaluation shows that the highly estimated odor of damascone (A, B) and damascenone (C) is more or less lost. This result can be explained by force-field calculation of the lowest energy conformation of 16, 19, and 21 in comparison with those of A-C. VCH Verlagsgesellschaft mbH, 1996.