36060-99-8 Usage
Chemical Class
Aromatic carboxylic acid methyl esters
Explanation
1-Naphthalenepropanoic acid methyl ester belongs to a class of chemical substances that are derived from aromatic compounds and contain a carboxylic acid group esterified with a methyl group.
Explanation
1-Naphthalenepropanoic acid methyl ester is synthesized from naphthalene, which is a polycyclic aromatic hydrocarbon consisting of two fused benzene rings.
Explanation
Due to its pleasant aroma, this chemical is widely used in the formulation of various personal care and fragrance products to provide a desirable scent.
Explanation
1-Naphthalenepropanoic acid methyl ester serves as a starting material or intermediate in the production of various pharmaceutical drugs, making it an important component in the pharmaceutical industry.
Explanation
1-Naphthalenepropanoic acid methyl ester is used to stabilize and prolong the scent of fragrances in products, ensuring that the aroma lasts longer and remains consistent.
Explanation
Research has shown that 1-Naphthalenepropanoic acid methyl ester may possess anti-inflammatory and pain-relieving properties, making it a potential candidate for the development of new drugs for pain relief and inflammation management.
Derivation
Naphthalene
Common Uses
Fragrance ingredient in perfumes, soaps, and cosmetics
Industrial Application
Intermediate in the synthesis of pharmaceuticals
Role
Fragrance fixative in products
Pharmacological Properties
Potential anti-inflammatory and analgesic properties
Check Digit Verification of cas no
The CAS Registry Mumber 36060-99-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,0,6 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 36060-99:
(7*3)+(6*6)+(5*0)+(4*6)+(3*0)+(2*9)+(1*9)=108
108 % 10 = 8
So 36060-99-8 is a valid CAS Registry Number.
36060-99-8Relevant academic research and scientific papers
The Stereochemistry of the Photochemical Rearrangement of 1-Substituted 1a,7b-Dihydro-1H-cyclopropanaphthalenes under Sensitized Conditions
Kato, Masahiko,Kobayashi, Hisako,Yamamoto, Hiroyuki,Seto, Koji,Ito, Satoru,,Miwa, Toshio
, p. 3523 - 3532 (2007/10/02)
The photolysis of 1-substituted 1a,7b-dihydro-1H-cyclopropanaphthalenes in the presence of Michler's ketone leads principally to 5-substituted 5H-benzocycloheptenes as primary products via a stepwise mechanism.The reaction proceeds smoothly with inversion of the migrating carbon if there is no steric hindrance, but it proceeds predominantly with retention if the inversion course is severely suppressed by steric hindrance.The marked difference in the exo-endo ratio of the secondary photocyclization products depending on the irradiation conditions was also recognized for 1-methoxycarbonylmethyl derivative.
