14939-92-5 Usage
General Description
3-(2,3-Dihydro-1,4-benzodioxin-6-yl)propanoic acid is a chemical compound that belongs to the class of phenylpropionic acids. It is a derivative of 2,3-dihydro-1,4-benzodioxin, which is a bicyclic chemical structure consisting of a benzene ring fused with a dioxin ring. 3-(2,3-DIHYDRO-1,4-BENZODIOXIN-6-YL)PROPANOIC ACID is commonly used in the pharmaceutical industry as a starting material for the synthesis of various drugs, including nonsteroidal anti-inflammatory drugs (NSAIDs) and other bioactive compounds. It is also known to have potential biological activities, such as anti-inflammatory and analgesic properties, making it a subject of interest in medicinal chemistry research. Additionally, 3-(2,3-dihydro-1,4-benzodioxin-6-yl)propanoic acid may have applications in other fields, such as organic synthesis and material science, due to its unique chemical structure and reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 14939-92-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,9,3 and 9 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 14939-92:
(7*1)+(6*4)+(5*9)+(4*3)+(3*9)+(2*9)+(1*2)=135
135 % 10 = 5
So 14939-92-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H12O4/c12-11(13)4-2-8-1-3-9-10(7-8)15-6-5-14-9/h1,3,7H,2,4-6H2,(H,12,13)
14939-92-5Relevant articles and documents
Pd-Catalyzed β-C(sp3)?H Arylation of Propionic Acid and Related Aliphatic Acids
Ghosh, Kiron K.,van Gemmeren, Manuel
supporting information, p. 17697 - 17700 (2017/12/07)
A generally applicable Pd-catalyzed protocol for the β-C(sp3)?H arylation of propionic acid and related α-branched aliphatic acids is reported. Enabled by the use of N-acetyl-β-alanine as ligand our protocol delivers a broad range of arylation products. Notably, the highly challenging substrate, propionic acid, which lacks any acceleration through the Thorpe–Ingold effect, can be employed as substrate with synthetically useful yields. Furthermore, the scalability and synthetic applicability of the protocol are demonstrated.
