74483-19-5 Usage
Chemical structure
1-phenylethyl 2-hydroxybenzoate is a derivative of benzoic acid, consisting of a phenylethyl group (C6H5-CH2-CH3) and a salicylate group (-OCO-C6H4-OH).
Usage in fragrance and flavor industry
It is commonly added to perfumes, colognes, and other scented products for its pleasant, floral aroma.
Preservative properties
1-phenylethyl 2-hydroxybenzoate acts as a preservative, extending the shelf life of various products.
Antioxidant potential
It has exhibited potential antioxidant properties, making it a valuable ingredient in cosmetic and skincare formulations.
Caution for sensitive individuals
This chemical should be used with caution, as it may cause irritation or allergic reactions in some individuals.
Check Digit Verification of cas no
The CAS Registry Mumber 74483-19-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,4,8 and 3 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 74483-19:
(7*7)+(6*4)+(5*4)+(4*8)+(3*3)+(2*1)+(1*9)=145
145 % 10 = 5
So 74483-19-5 is a valid CAS Registry Number.
74483-19-5Relevant academic research and scientific papers
POLYMERIZABLE MONOMERS AND METHOD OF POLYMERIZING THE SAME
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Paragraph 0174-0176; 0242-0244, (2019/11/19)
Provided herein are photopolymerizable monomers, optionally for use as reactive diluents in a high temperature lithography-based photopolymerization process, a method of producing polymers using said photopolymerizable monomers, the polymers thus produced, and orthodontic appliances comprising the polymers.
Enzymatic hydrolyses of acetoxy- and phenethylbenzoates by Candida cylindracea lipase
Cipiciani, Antonio,Fringuelli, Francesco,Scappini, Anna Maria
, p. 9869 - 9876 (2007/10/03)
The lipase from Candida cylindracea (CCL) deacctyles rapidly and selective all three regioisomer methyl acctoxybenzoates. In the enzymatic hydrolyses of analogous aryl acctoxybenzoates, the difference of reactivity between the acetoxy and benzoloxy funcionalities is reduced and a aspirin- like prodrugs. The degree of enantioselectivity of the enzymatic hydrolysis of phenethylbenzoates is related to the position of the stereogenic center.
