90034-85-8 Usage
Description
ETHYL(2-IODOBENZOYL)ACETATE is a chemical compound with the formula C11H11IO3, characterized as an ester formed by the reaction of acetic acid and 2-iodobenzoyl chloride. This white crystalline solid possesses a molecular weight of 314.10 g/mol and a melting point of 37-39 °C. Its aromatic properties and utility in organic synthesis make it a valuable component in the production of pharmaceuticals, agrochemicals, perfumes, and flavorings.
Uses
Used in Pharmaceutical Industry:
ETHYL(2-IODOBENZOYL)ACETATE is used as a building block for the synthesis of various pharmaceuticals, contributing to the development of new medications and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, ETHYL(2-IODOBENZOYL)ACETATE serves as a key component in the production of agrochemicals, aiding in the creation of pesticides and other agricultural products to enhance crop protection and yield.
Used in Perfume Industry:
ETHYL(2-IODOBENZOYL)ACETATE is utilized as an aromatic compound in the manufacturing of perfumes, adding unique scents and enhancing the overall fragrance profile of various perfume products.
Used in Flavoring Industry:
This chemical compound is also employed in the flavoring industry to create and modify flavors for food and beverages, capitalizing on its aromatic properties to improve taste experiences.
It is crucial to handle ETHYL(2-IODOBENZOYL)ACETATE with care due to its potential harmful effects if ingested, inhaled, or comes into contact with skin.
Check Digit Verification of cas no
The CAS Registry Mumber 90034-85-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,0,3 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 90034-85:
(7*9)+(6*0)+(5*0)+(4*3)+(3*4)+(2*8)+(1*5)=108
108 % 10 = 8
So 90034-85-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H11IO3/c1-2-15-11(14)7-10(13)8-5-3-4-6-9(8)12/h3-6H,2,7H2,1H3
90034-85-8Relevant articles and documents
Palladium-Catalyzed Asymmetric Intramolecular Reductive Heck Desymmetrization of Cyclopentenes: Access to Chiral Bicyclo[3.2.1]octanes
Yuan, Zhenbo,Feng, Ziwen,Zeng, Yuye,Zhao, Xiaobin,Lin, Aijun,Yao, Hequan
supporting information, p. 2884 - 2888 (2019/02/16)
A palladium-catalyzed asymmetric reductive Heck reaction of unactivated aliphatic alkenes, with eliminable β-hydrogen atoms, has been realized for the first time. A series of optically active bicyclo[3.2.1]octanes bearing chiral quaternary and tertiary carbon stereocenters were obtained in good yields with excellent enantioselectivities, exhibiting good functional-group tolerance and scalability. Moreover, deuterated optically active bicyclo[3.2.1]octanes were also obtained in high efficiency.
4-quinolone derivatives having anti-inflammatory, anti-allergic, antitussive, expectorant and antithrombotic activity
-
, (2008/06/13)
4-Quinolone derivatives of the present invention are useful for their anti-inflammatory, anti-allergenic, antitussive, expectorant and antithrombotic activity. Pharmaceutical compositions containing said compounds and pharmaceutically acceptable salts thereof and methods of treating humans and animals are described herein.
