61349-69-7 Usage
Description
Cyclopentanone, 2-(4-methoxyphenyl)-, also known as 4'-methoxyacetophenone, is a chemical compound that belongs to the class of aromatic ketones. It is a colorless to pale yellow liquid with a sweet, floral, and fruity odor. Cyclopentanone, 2-(4-methoxyphenyl)is commonly used as a building block in the synthesis of various pharmaceuticals, agrochemicals, and organic compounds.
Uses
Used in Pharmaceutical Industry:
Cyclopentanone, 2-(4-methoxyphenyl)is used as a building block for the synthesis of various pharmaceuticals. Its unique chemical structure allows it to be a versatile component in the development of new drugs and medications.
Used in Agrochemical Industry:
Cyclopentanone, 2-(4-methoxyphenyl)is also used as a building block in the synthesis of agrochemicals, contributing to the development of new pesticides, herbicides, and other agricultural products.
Used in Organic Compounds Synthesis:
Cyclopentanone, 2-(4-methoxyphenyl)is utilized as a building block in the synthesis of various organic compounds, expanding its applications in different fields of chemistry.
Used in Fragrance Industry:
It is primarily used as a fragrance ingredient in cosmetic and personal care products, as well as in flavorings and fragrances, due to its sweet, floral, and fruity odor.
Used as a Solvent:
Cyclopentanone, 2-(4-methoxyphenyl)is also used as a solvent and intermediate in the production of other chemicals, further broadening its applications across various industries.
It is important to handle this compound with care, as it may pose health hazards, and should be used in accordance with proper safety guidelines and regulations.
Check Digit Verification of cas no
The CAS Registry Mumber 61349-69-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,3,4 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 61349-69:
(7*6)+(6*1)+(5*3)+(4*4)+(3*9)+(2*6)+(1*9)=127
127 % 10 = 7
So 61349-69-7 is a valid CAS Registry Number.
61349-69-7Relevant articles and documents
Enantioselective Radical Ring-Opening Cyanation of Oxime Esters by Dual Photoredox and Copper Catalysis
Chen, Jun,Wang, Peng-Zi,Lu, Bin,Liang, Dong,Yu, Xiao-Ye,Xiao, Wen-Jing,Chen, Jia-Rong
supporting information, p. 9763 - 9768 (2019/11/29)
Catalytic enantioselective chemical reactions involving highly reactive radical species remain largely unexplored. We report herein for the first time a novel enantioselective radical ring-opening cyanation of redox-active oxime esters by dual photoreodox
Regio- and enantioselective Baeyer-Villiger oxidation: Kinetic resolution of racemic 2-substituted cyclopentanones
Zhou, Lin,Liu, Xiaohua,Ji, Jie,Zhang, Yuheng,Wu, Wangbin,Liu, Yangbin,Lin, Lili,Feng, Xiaoming
supporting information, p. 3938 - 3941 (2014/08/18)
A kinetic resolution of racemic 2-substituted cyclopentanones via highly regio- and enantioselective Baeyer-Villiger oxidation has been successfully developed. The reaction could afford the normal 6-substituted δ-lactones in up to 98% ee and >19/1 regioselectivity. Meanwhile, the unreacted ketones were recovered in excellent ee values (up to 98%). It represents the best results of the kinetic resolution of racemic 2-substituted cyclopentanones via nonenzymic asymmetric BV oxidation.
The 2-(2-Azidoethyl)cycloalkanone strategy for bridged amides and medium-sized cyclic amine derivatives in the Aubé-Schmidt reaction
Macleod, Fraser,Lang, Stuart,Murphy, John A.
supporting information; experimental part, p. 529 - 534 (2010/10/02)
2-(2-Azidoethyl)cycloalkanones afford bridged lactams in the Aubé-Schmidt reaction, sometimes in excellent yield, and solvolysis yields derivatives of medium-ring amines. Attempts to divert the Schmidt reaction with an arene-mediated fragmentation of the normal Schmidt intermediate have led to an initial example. Georg Thieme Verlag Stuttgart.
