34824-58-3 Usage
Description
2-(2-BROMOPHENYL)-1,3-DIOXOLANE is an organic compound that serves as a crucial intermediate in various chemical syntheses. It is characterized by its clear colorless to pale yellow liquid appearance and is known for its significance in the production of various compounds across different industries.
Uses
Used in Organic Synthesis:
2-(2-BROMOPHENYL)-1,3-DIOXOLANE is used as a key intermediate for the synthesis of a wide range of organic compounds. Its unique structure allows for versatile reactions, making it a valuable component in the creation of new molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 2-(2-BROMOPHENYL)-1,3-DIOXOLANE is utilized as a vital building block for the development of various drugs. Its incorporation into drug molecules can enhance their efficacy and pharmacological properties, contributing to the advancement of novel therapeutic agents.
Used in Agrochemicals:
2-(2-BROMOPHENYL)-1,3-DIOXOLANE is employed as a raw material in the agrochemical industry, where it is used to produce compounds with pesticidal, herbicidal, and fungicidal properties. Its role in the synthesis of these agrochemicals helps to improve crop protection and yield.
Used in Dye Industry:
In the dyestuffs industry, 2-(2-BROMOPHENYL)-1,3-DIOXOLANE is used as an essential raw material for the production of various dyes. Its chemical properties enable the creation of dyes with specific color characteristics and improved performance, catering to the diverse needs of the textile and other related industries.
Check Digit Verification of cas no
The CAS Registry Mumber 34824-58-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,8,2 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 34824-58:
(7*3)+(6*4)+(5*8)+(4*2)+(3*4)+(2*5)+(1*8)=123
123 % 10 = 3
So 34824-58-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H9BrO2/c10-8-4-2-1-3-7(8)9-11-5-6-12-9/h1-4,9H,5-6H2
34824-58-3Relevant articles and documents
Conformational diastereoisomerism in tris-( 2-alkylimino) triphenylphosphines
Whitnall, Mark R.,Hii, King Kuok Mimi,Thornton-Pett, Mark,Kee, Terence P.
, p. 35 - 50 (1997)
A combination of one-dimensional, two-dimensional and nuclear Overhauser experiments allow complete NMR spectroscopic characterisation of the trifunctionalised triphenylphosphine, tris-(2-carboxaldehyde)triphenylphosphine 1. A single-crystal X-ray diffrac
Cobalt-Catalyzed Chemoselective Transfer Hydrogenative Cyclization Cascade of Enone-Tethered Aldehydes
Ma, Shuang-Shuang,Jiang, Biao-Ling,Yu, Zheng-Kun,Zhang, Suo-Jiang,Xu, Bao-Hua
supporting information, p. 3873 - 3878 (2021/05/26)
The ligand-free Co-catalyzed chemoselective reductive cyclization cascade of enone-tethered aldehydes with i-PrOH as the environmentally benign hydrogen surrogate is developed by this study. Mechanistic studies disclosed that such a protocol is initiated
Annulative Morita-Baylis-Hillman reaction to synthesise chiral dibenzocycloheptanes
Mondal, Atanu,Ramasastry, S. S. V.,Shivangi,Tung, Pinku,Wagulde, Siddhant V.
supporting information, p. 9260 - 9263 (2021/09/20)
We describe the first metal-free and organocatalytic strategy to access highly functionalised dibenzocycloheptanesviaa phosphine-promoted annulative Morita-Baylis-Hillman (MBH) reaction. The method is manipulated to access to chiral dibenzocycloheptanes as well. This work represents a rare entry for the construction of seven-membered carbocyclesviathe MBH route. The realisation of several bioactive molecules possessing the dibenzocycloheptane core makes this an attractive strategy.
