16231-67-7 Usage
Description
Methyl 2-(2-formylphenyl)benzoate is an organic compound derived from benzoic acid, featuring a methyl ester group, a benzene ring, and a formyl group. It serves as a versatile intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds, while also finding applications in the production of fragrances and as a flavoring agent in the food industry. Due to its potentially hazardous nature, it requires careful handling to prevent skin, eye, and respiratory irritation.
Uses
Used in Pharmaceutical Industry:
Methyl 2-(2-formylphenyl)benzoate is used as a key intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
methyl 2-(2-formylphenyl)benzoate is utilized as an intermediate in the production of agrochemicals, playing a role in the creation of pesticides and other agricultural products to enhance crop protection and yield.
Used in Fragrance Production:
Methyl 2-(2-formylphenyl)benzoate is employed as a component in the production of fragrances, adding unique scents and enhancing the overall aroma of perfumes, colognes, and other scented products.
Used in Food Industry:
As a flavoring agent, methyl 2-(2-formylphenyl)benzoate is used to impart specific tastes and flavors to food products, enriching the sensory experience of consumers.
Used in Chemical Research:
methyl 2-(2-formylphenyl)benzoate serves as a valuable research tool in the field of organic chemistry, aiding scientists in understanding chemical reactions and developing new synthetic pathways.
Check Digit Verification of cas no
The CAS Registry Mumber 16231-67-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,2,3 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 16231-67:
(7*1)+(6*6)+(5*2)+(4*3)+(3*1)+(2*6)+(1*7)=87
87 % 10 = 7
So 16231-67-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H12O3/c1-18-15(17)14-9-5-4-8-13(14)12-7-3-2-6-11(12)10-16/h2-10H,1H3
16231-67-7Relevant articles and documents
-
Bailey
, p. 3811,3815 (1956)
-
Atroposelective Synthesis of Axially Chiral Biaryls by Palladium-Catalyzed Asymmetric C?H Olefination Enabled by a Transient Chiral Auxiliary
Yao, Qi-Jun,Zhang, Shuo,Zhan, Bei-Bei,Shi, Bing-Feng
supporting information, p. 6617 - 6621 (2017/05/29)
Atroposelective synthesis of axially chiral biaryls by palladium-catalyzed C?H olefination, using tert-leucine as an inexpensive, catalytic, and transient chiral auxiliary, has been realized. This strategy provides a highly efficient and straightforward access to a broad range of enantioenriched biaryls in good yields (up to 98 %) with excellent enantioselectivities (95 to >99 % ee). Kinetic resolution of trisubstituted biaryls bearing sterically more demanding substituents is also operative, thus furnishing the optically active olefinated products with excellent selectivity (95 to >99 % ee, s-factor up to 600).
A microwave-assisted diastereoselective multicomponent reaction to access dibenzo[ c, e ]azepinones: Synthesis and biological evaluation
Mehta, Vaibhav P.,Modha, Sachin G.,Ruijter, Eelco,Van Hecke, Kristof,Van Meervelt, Luc,Pannecouque, Christophe,Balzarini, Jan,Orru, Romano V. A.,Van Der Eycken, Erik
supporting information; experimental part, p. 2828 - 2839 (2011/06/26)
An unprecedented microwave-assisted multicomponent strategy has been elaborated for the fast, efficient, and diastereoselective generation of the dibenzo[c,e]azepinone scaffold. The generated compounds were evaluated for their bioactivity.
