15805-98-8 Usage
Uses
Used in Organic Synthesis:
2-(acetyloxy)-2-methylpropanoic acid is used as a reagent in organic synthesis for the preparation of various organic compounds. Its unique chemical structure allows it to participate in a range of reactions, contributing to the synthesis of diverse organic molecules.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 2-(acetyloxy)-2-methylpropanoic acid is used as a key intermediate in the synthesis of drugs. Its versatility in chemical reactions enables the creation of new pharmaceutical compounds with potential therapeutic applications.
Used in Agrochemical Production:
2-(acetyloxy)-2-methylpropanoic acid also finds application in the agrochemical sector, where it is used in the development of pesticides and other agricultural chemicals. Its role in these products is crucial for enhancing crop protection and yield.
Safety Precautions:
Given the potential hazards associated with 2-(acetyloxy)-2-methylpropanoic acid, it is essential to handle 2-(acetyloxy)-2-methylpropanoic acid with care. Protective equipment such as gloves, goggles, and masks should be worn during its use to minimize the risk of ingestion, inhalation, or skin contact. Proper disposal and storage methods should also be followed to ensure safety in the workplace.
Check Digit Verification of cas no
The CAS Registry Mumber 15805-98-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,8,0 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 15805-98:
(7*1)+(6*5)+(5*8)+(4*0)+(3*5)+(2*9)+(1*8)=118
118 % 10 = 8
So 15805-98-8 is a valid CAS Registry Number.
15805-98-8Relevant academic research and scientific papers
A highly selective, high-speed, and hydrolysis-free O-acylation in subcritical water in the absence of a catalyst
Sato, Masahiro,Matsushima, Keiichiro,Kawanami, Hajime,Ikuhsima, Yutaka
, p. 6284 - 6288 (2008/04/05)
(Chemical Equation Presented) Fast and furious: A wide range of alcohols are acylated by acetic anhydride, in the absence of catalyst, in subcritical water in a flow-type microreaction system. The esters are selectively produced in high yields at temperatures of 200 to 250°C. Varying the amount of acetic anhydride added with respect to the alcohols allows the regioselective acylation of one or both hydroxy groups of various dihydroxy compounds (see picture).
