132545-15-4 Usage
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
Design and synthesis of novel xanthine derivatives as potent and selective A2B adenosine receptor antagonists for the treatment of chronic inflammatory airway diseases
Basu, Sujay,Barawkar, Dinesh A.,Ramdas, Vidya,Patel, Meena,Waman, Yogesh,Panmand, Anil,Kumar, Santosh,Thorat, Sachin,Naykodi, Minakshi,Goswami, Arnab,Reddy, B. Srinivasa,Prasad, Vandna,Chaturvedi, Sandhya,Quraishi, Azfar,Menon, Suraj,Paliwal, Shalini,Kulkarni, Abhay,Karande, Vikas,Ghosh, Indraneel,Mustafa, Syed,De, Siddhartha,Jain, Vaibhav,Banerjee, Ena Ray,Rouduri, Sreekanth R.,Palle, Venkata P.,Chugh, Anita,Mookhtiar, Kasim A.
, p. 218 - 229 (2017/04/19)
Adenosine induces bronchial hyperresponsiveness and inflammation in asthmatics through activation of A2B adenosine receptor (A2BAdoR). Selective antagonists have been shown to attenuate airway reactivity and improve inflammatory cond
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