881190-93-8 Usage
Description
3-(3-Chloro-4-fluorophenyl)propanoic acid is an organic compound characterized by the presence of a chloro and a fluoro substituent on a phenyl ring attached to a propanoic acid group. This unique structure endows it with versatile reactivity and synthetic utility in various chemical processes.
Uses
Used in Organic Synthesis:
3-(3-Chloro-4-fluorophenyl)propanoic acid serves as a valuable reactant in organic synthesis, particularly for the preparation of pharmaceuticals, agrochemicals, and other specialty chemicals. Its distinct functional groups allow for a range of reactions, such as nucleophilic substitutions, electrophilic aromatic substitutions, and coupling reactions, facilitating the creation of diverse molecular architectures.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-(3-chloro-4-fluorophenyl)propanoic acid is utilized as a key intermediate in the synthesis of various drug molecules. Its unique structural features enable the development of new drugs with improved potency, selectivity, and pharmacokinetic properties. 3-(3-CHLORO-4-FLUOROPHENYL)PROPIONIC ACID's reactivity and functional group compatibility make it an attractive building block for medicinal chemists.
Used in Agrochemical Industry:
3-(3-Chloro-4-fluorophenyl)propanoic acid also finds application in the agrochemical industry, where it is employed in the synthesis of novel pesticides and herbicides. Its ability to form a wide array of derivatives allows for the development of more effective and targeted agrochemicals, contributing to enhanced crop protection and yield.
Check Digit Verification of cas no
The CAS Registry Mumber 881190-93-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,1,1,9 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 881190-93:
(8*8)+(7*8)+(6*1)+(5*1)+(4*9)+(3*0)+(2*9)+(1*3)=188
188 % 10 = 8
So 881190-93-8 is a valid CAS Registry Number.
881190-93-8Relevant articles and documents
Indanylidenes. 2. Design and synthesis of (E)-2-(4-chloro-6-fluoro-1-indanylidene)-N-methylacetamide, a potent antiinflammatory and analgesic agent without centrally acting muscle relaxant activity
Musso, David L.,Orr, G. Faye,Cochran, Felicia R.,Kelley, James L.,Selph, Jeffrey L.,Rigdon, Greg C.,Cooper, Barrett R.,Jones, Michael L.
, p. 409 - 416 (2007/10/03)
Extension of the structure-activity relationship studies that led to the discovery of the nonsedating potent muscle relaxant, antiinflammatory, and analgesic agent (E)-2-(4,6-difluoro-1-indanylidene)acetamide, 1, has given rise to (E)-2-(4-chloro-6-fluoro
