98070-39-4 Usage
Uses
Used in Pharmaceutical Industry:
2-CHLORO-3-HYDROXYPROPIONIC ACID METHYL ESTER is used as an intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the formation of complex molecular structures required for drug development.
Used in Agrochemical Industry:
In the agrochemical sector, 2-CHLORO-3-HYDROXYPROPIONIC ACID METHYL ESTER is utilized as an intermediate in the production of agrochemicals, playing a role in the development of compounds that can enhance crop protection and yield.
Used in Organic Chemistry:
2-CHLORO-3-HYDROXYPROPIONIC ACID METHYL ESTER is used as a reagent in organic chemistry reactions, facilitating specific transformations and syntheses that are essential for creating a wide range of organic compounds.
Used in Chemical Production:
As a building block, 2-CHLORO-3-HYDROXYPROPIONIC ACID METHYL ESTER is employed in the production of other chemicals, contributing to the synthesis of various compounds used across different industries.
Safety Note:
It is important to handle 2-CHLORO-3-HYDROXYPROPIONIC ACID METHYL ESTER with care due to its corrosive nature, which may cause irritation to the skin, eyes, and respiratory system. Proper safety measures should be taken during its use and storage to minimize potential hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 98070-39-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,0,7 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 98070-39:
(7*9)+(6*8)+(5*0)+(4*7)+(3*0)+(2*3)+(1*9)=154
154 % 10 = 4
So 98070-39-4 is a valid CAS Registry Number.
InChI:InChI=1/C4H7ClO3/c1-8-4(7)3(5)2-6/h3,6H,2H2,1H3
98070-39-4Relevant academic research and scientific papers
(2,6-Dichloro-4-alkoxyphenyl)-(2,4-dichlorophenyl)methyl trichloroacetimidates: Protection of alcohols and carboxylic acids in solution or on polymer support
Kurosu, Michio,Li, Kai
experimental part, p. 3633 - 3641 (2010/03/05)
(2,6-Dichloro-4-methoxyphenyl)-(2,4-dichlorophenyl)-methyl trichloroacetimidate can be efficiently activated by TMSOTf (10-100 mol%) to react with alcohols and carboxylic acids. Under these conditions a wide variety of alcohols can be transformed into the corresponding ethers in excellent yields with a slight excess of the trichloroacetimidate. The resulting ethers are not susceptible to typical deprotection conditions for benzyl and 4-methoxybenzyl ether groups, however, they can be conveniently deprotected by treatment with 30-50% trifluoroacetic acid in dichloromethane. Polymer-bound (2,6-dichloro-4-alkoxyphenyl)-(2,4-dichlorophenyl)methyl trichloroacetimidate is useful for immobilization of alcohols and carboxylic acids.
