132545-15-4 Usage
Description
3-(3-Hydroxy-prop-1-ynyl)-benzoic acid, a derivative of benzoic acid, is a chemical compound characterized by its molecular formula C10H8O3. It features a propynyloxy group and a hydroxy group attached to the benzene ring, endowing it with unique chemical properties. 3-(3-HYDROXY-PROP-1-YNYL)-BENZOIC ACID is recognized for its potential anti-inflammatory and antioxidant properties, as well as its promising applications in the fields of medicine and organic chemistry.
Uses
Used in Organic Synthesis:
3-(3-Hydroxy-prop-1-ynyl)-benzoic acid is utilized as a building block in organic synthesis, providing a versatile starting material for the creation of various complex organic molecules. Its unique structure allows for a wide range of chemical reactions, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Applications:
3-(3-Hydroxy-prop-1-ynyl)-benzoic acid is employed as a potential therapeutic agent due to its anti-inflammatory and antioxidant properties. These characteristics make it a candidate for the development of new drugs to treat various inflammatory and oxidative stress-related conditions.
Used in Medical Applications:
3-(3-HYDROXY-PROP-1-YNYL)-BENZOIC ACID has been investigated for its potential use in the treatment of neurological and neurodegenerative disorders. Its ability to modulate neuroinflammation suggests that it could play a role in managing conditions such as Alzheimer's disease, Parkinson's disease, and multiple sclerosis.
Used in Antioxidant Formulations:
Given its antioxidant properties, 3-(3-Hydroxy-prop-1-ynyl)-benzoic acid can be used in formulations designed to protect cells from oxidative damage, which is implicated in a variety of diseases and aging processes.
Used in Anti-Inflammatory Agents:
The anti-inflammatory potential of 3-(3-Hydroxy-prop-1-ynyl)-benzoic acid makes it a candidate for the development of new anti-inflammatory drugs, which could be used to treat conditions such as arthritis, asthma, and other inflammatory disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 132545-15-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,5,4 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 132545-15:
(8*1)+(7*3)+(6*2)+(5*5)+(4*4)+(3*5)+(2*1)+(1*5)=104
104 % 10 = 4
So 132545-15-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H8O3/c11-6-2-4-8-3-1-5-9(7-8)10(12)13/h1,3,5,7,11H,6H2,(H,12,13)
132545-15-4Relevant articles and documents
REACTIONS OF PROPARGYL ALCOHOL WITH ARYL IODIDES CATALYZED BY PALLADIUM COMPLEXES IN WATER
Bumagin, N. A.,Bykov, V. V.,Beletskaya, I. P.
, p. 2418 (1990)
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Palladium-Catalyzed Reaction of 2-Propynyl Alcohol with Aryl Iodides in Water
Bumagin, N. A.,Bykov, V. V.,Beletskaya, I. P.
, p. 348 - 350 (2007/10/03)
The reaction of 2-propynyl alcohol with aryl iodides in aqueous media in the presence of various palladium compounds and bases was studied.High yields of 3-aryl-2-propynyl alcohols were obtained in water in the presence of triethylamine as a base and cata
