24509-88-4 Usage
Chemical compound
Yes
Found in
Essential oils of fruits and flowers
Physical state
Clear, colorless liquid
Aroma
Sweet, floral, and fruity
Industry use
Fragrance industry, food industry, pharmaceutical and cosmetic industries
Fragrance industry role
Natural constituent of various essential oils, providing a pleasant, sweet, and fruity scent
Food industry role
Flavoring agent in baked goods, beverages, and candies, adding a fruity and floral note
Pharmaceutical and cosmetic industries role
Used for its aromatic and antimicrobial properties
Safety
Considered safe for use in food and cosmetics when used in accordance with regulations
Check Digit Verification of cas no
The CAS Registry Mumber 24509-88-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,5,0 and 9 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 24509-88:
(7*2)+(6*4)+(5*5)+(4*0)+(3*9)+(2*8)+(1*8)=114
114 % 10 = 4
So 24509-88-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H12O2/c1-5-7(3,4)9-6(2)8/h5H,1H2,2-4H3
24509-88-4Relevant articles and documents
Catalytic asymmetric synthesis of chiral allylic esters
Cannon, Jeffrey S.,Kirsch, Stefan F.,Overman, Larry E.
supporting information; experimental part, p. 15185 - 15191 (2010/12/25)
A broadly useful catalytic enantioselective synthesis of branched allylic esters from prochiral (Z)-2-alkene-1-ols has been developed. The starting allylic alcohol is converted to its trichloroacetimidate intermediate by reaction with trichloroacetonitrile, either in situ or in a separate step, and this intermediate undergoes clean enantioselective SN2′ substitution with a variety of carboxylic acids in the presence of the palladium(II) catalyst (Rp,S)-di-μ-acetatobis[(η5- 2-(2′-(4′-methylethyl)oxazolinyl)cyclopentadienyl-1-C,3′-N) (η4-tetraphenylcyclobutadiene)cobalt]dipalladium, (R p,S)-[COP-OAc]2, or its enantiomer. The scope and limitations of this useful catalytic asymmetric allylic esterification are defined.
