90482-29-4 Usage
Uses
Used in Pharmaceutical Research and Development:
4-OXO-2-CARBOXYCYCLOHEPTANE is utilized as a key building block in pharmaceutical research for the synthesis of novel drug candidates. Its unique structure and reactivity allow for the creation of compounds with potential therapeutic applications, contributing to the advancement of new treatments for various diseases and conditions.
Used in Organic Synthesis:
In the field of organic synthesis, 4-OXO-2-CARBOXYCYCLOHEPTANE serves as an important intermediate. Its presence in the synthesis process can lead to the formation of complex organic molecules with specific functionalities, which are essential in various chemical and material applications.
Used in Fragrance and Flavoring Agent Production:
4-OXO-2-CARBOXYCYCLOHEPTANE is also used as an intermediate in the production of fragrance compounds and flavoring agents. Its chemical properties allow for the development of unique scents and tastes that can be incorporated into a wide range of consumer products, from perfumes and cosmetics to food and beverages.
Used in the Development of Functional Materials:
4-OXO-2-CARBOXYCYCLOHEPTANE's structural and chemical attributes make it a candidate for the development of functional materials with specific properties. These materials could have applications in various industries, such as electronics, where they might be used in the creation of sensors or other components that require unique chemical interactions.
Check Digit Verification of cas no
The CAS Registry Mumber 90482-29-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,4,8 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 90482-29:
(7*9)+(6*0)+(5*4)+(4*8)+(3*2)+(2*2)+(1*9)=134
134 % 10 = 4
So 90482-29-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H12O3/c9-7-4-2-1-3-6(5-7)8(10)11/h6H,1-5H2,(H,10,11)
90482-29-4Relevant academic research and scientific papers
Last of the gem-Difluorocycloalkanes 2: Synthesis of Fluorinated Cycloheptane Building Blocks
Herasymchuk, Maksym,Melnykov, Kostiantyn P.,Yarmoliuk, Dmytro V.,Serhiichuk, Dmytro,Rotar, Valeriia,Pukhovoi, Timur,Kuchkovska, Yuliya O.,Holovach, Sergey,Volochnyuk, Dmitriy M.,Ryabukhin, Sergey V.,Grygorenko, Oleksandr O.
, p. 6561 - 6569 (2021/02/16)
The gem-difluorocycloalkane family was extended to all possible regioisomers of the gem-difluorocycloheptane, monofunctionalized by carboxilic-, amino- or keto- group, that were synthesized on a multigram scale. The preparation of the corresponding building blocks was achieved from readily accessible starting materials either via six-membered ring homologation or deoxofluorination of the appropriate seven-membered cyclic ketones.
