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24303-64-8

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24303-64-8 Usage

Description

4-Methoxy-but-2-ynoic acid is a chemical compound with the molecular formula C6H8O3. It is a derivative of butynoic acid, containing a methoxy group (-OCH3) attached to the carbon atom in the fourth position of the butynoic acid chain. As a carboxylic acid, it contains a carboxyl group (-COOH) and exhibits acidic properties. 4-Methoxy-but-2-ynoic acid serves as a versatile building block in organic synthesis and holds potential for applications in various fields, including pharmaceuticals, agrochemicals, and medicinal chemistry, due to its unique structural properties and possible biological activities.

Uses

Used in Organic Synthesis:
4-Methoxy-but-2-ynoic acid is used as a building block in organic synthesis for the creation of a wide range of chemical products. Its unique structure allows for the development of novel compounds with specific properties, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 4-Methoxy-but-2-ynoic acid is utilized as a key intermediate in the synthesis of various drugs. Its acidic nature and structural features enable the production of molecules with specific therapeutic effects, contributing to the development of new medications.
Used in Agrochemical Development:
4-Methoxy-but-2-ynoic acid is employed in the agrochemical sector as a precursor for the synthesis of pesticides, herbicides, and other crop protection agents. Its chemical properties allow for the creation of effective and targeted agrochemicals that can improve agricultural productivity and crop protection.
Used in Medicinal Chemistry Research:
Due to its potential biological activities and structural properties, 4-Methoxy-but-2-ynoic acid is used in medicinal chemistry research to explore its therapeutic potential. It may serve as a starting point for the development of new drugs or as a tool to understand the mechanisms of action of existing medications.

Check Digit Verification of cas no

The CAS Registry Mumber 24303-64-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,3,0 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 24303-64:
(7*2)+(6*4)+(5*3)+(4*0)+(3*3)+(2*6)+(1*4)=78
78 % 10 = 8
So 24303-64-8 is a valid CAS Registry Number.

24303-64-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methoxybut-2-ynoic acid

1.2 Other means of identification

Product number -
Other names 4-Methoxy-tetrolsaeure

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:24303-64-8 SDS

24303-64-8Relevant articles and documents

Carboxylation of Terminal Alkynes with Carbon Dioxide Catalyzed by an In Situ Ag2O/N-Heterocyclic Carbene Precursor System

Yuan, Ye,Chen, Cheng,Zeng, Cheng,Mousavi, Bibimaryam,Chaemchuen, Somboon,Verpoort, Francis

, p. 882 - 887 (2017/03/13)

A carboxylation of terminal alkynes with carbon dioxide (CO2) at ambient conditions was developed in situ using a series of N-heterocyclic carbene (NHC) precursors and Ag2O. The unique structure of NHCs largely increases the solubility of active Ag species and meanwhile activates CO2 by forming the NHC–CO2 adduct. This novel catalytic system demonstrated quite low Ag loading, very high activities, wide substrate generality and excellent tolerance for a variety of functionalities. In addition, avoiding cumbersome synthesis procedures, processing, and reserving of the photosensitive Ag complex, this system could be stored and operated as straightforward as the inorganic Ag salt catalysts.

OXAZOLIDINONE HYDROXAMIC ACID COMPOUNDS FOR THE TREATMENT OF BACTERIAL INFECTIONS

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Page/Page column 94, (2015/05/19)

This invention pertains generally to treating bacterial infections using organic compounds of Formula I. In certain aspects, the invention pertains to treating infections caused by Gram-negative bacteria. (I) wherein X, Y, R1, R2, R3, R4 and R5 and defined herein.

4 - IMIDAZOPYRIDAZIN- 1 -YL-BENZAMIDES AND 4 - IMIDAZOTRIAZIN- 1 - YL - BENZAMIDES AS BTK- INHIBITORS

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Page/Page column 77, (2013/03/26)

The present invention relates to 6-5 membered fused pyridine ring compounds according to formula (I) or a pharmaceutically acceptable salt thereof or to pharmaceutical compositions comprising these compounds and to their use in therapy. In particular, the present invention relates to the use of 6-5 membered fused pyridine ring compounds according to formula I in the treatment of Brutons Tyrosine Kinase (Btk) mediated disorders.

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