52513-03-8 Usage
Description
2-methylbutyl benzoate is a chemical compound that belongs to the ester group, formed from the reaction of 2-methyl-1-butanol and benzoic acid. It is typically clear or pale yellow in color, and has a pleasant odor resembling that of apples or strawberries. This chemical is known for its low toxicity and is considered safe for use in food and cosmetic applications.
Uses
Used in Food Industry:
2-methylbutyl benzoate is used as a flavoring agent for its sweet, fruity, and slightly floral aroma.
Used in Perfume and Fragrance Industry:
2-methylbutyl benzoate is used in the production of perfumes and fragrances due to its pleasant odor.
Used in Cosmetics and Personal Care Products:
2-methylbutyl benzoate is used in the manufacture of cosmetics and personal care products for its desirable scent and low toxicity.
Check Digit Verification of cas no
The CAS Registry Mumber 52513-03-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,5,1 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 52513-03:
(7*5)+(6*2)+(5*5)+(4*1)+(3*3)+(2*0)+(1*3)=88
88 % 10 = 8
So 52513-03-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H16O2/c1-3-10(2)9-14-12(13)11-7-5-4-6-8-11/h4-8,10H,3,9H2,1-2H3
52513-03-8Relevant articles and documents
Silver-mediated oxidative aliphatic C-H trifluoromethylthiolation
Guo, Shuo,Zhang, Xiaofei,Tang, Pingping
supporting information, p. 4065 - 4069 (2015/03/30)
The first example of a practical and direct trifluoromethylthiolation reaction of unactivated aliphatic C-H bonds employs a silver-based reagent. The reaction is operationally simple, scalable, and proceeds under aqueous conditions in air. Furthermore, its broad scope and good functional-group compatibility were demonstrated by applying this method to the selective trifluoromethylthiolation of natural products and natural-product derivatives.
