1121-62-6 Usage
Description
4-CHLOROMETHYL-[1,3]DIOXANE is a chlorinated derivative of dioxane, a heterocyclic organic compound with the molecular formula C4H7ClO2. It is recognized for its versatility in chemical reactions and is commonly used as a solvent and in the synthesis of other organic compounds.
Uses
Used in Pharmaceutical Industry:
4-CHLOROMETHYL-[1,3]DIOXANE is used as a solvent and in the synthesis of pharmaceutical compounds due to its ability to facilitate various chemical reactions, contributing to the development of new drugs and medications.
Used in Agricultural Industry:
In agriculture, 4-CHLOROMETHYL-[1,3]DIOXANE is utilized as a solvent and in the synthesis of agrochemicals, aiding in the production of effective pesticides and other agricultural products to enhance crop protection and yield.
Used in Manufacturing Industry:
4-CHLOROMETHYL-[1,3]DIOXANE serves as a versatile component in the manufacturing of various organic compounds, playing a crucial role in the production of different industrial chemicals and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 1121-62-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,2 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1121-62:
(6*1)+(5*1)+(4*2)+(3*1)+(2*6)+(1*2)=36
36 % 10 = 6
So 1121-62-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H9ClO2/c6-3-5-1-2-7-4-8-5/h5H,1-4H2/t5-/m0/s1
1121-62-6Relevant articles and documents
Condensation of 1,2,4-Butanetriol with Carbonyl Compounds and Reactions of Hydroxyalkyl-1,3-dioxacyclanes
Raskil’dina,Borisova, Yu. G.,Zlotskii
, p. 1601 - 1605 (2018)
A mixture of isomers of 2-(1,3-dioxolan-4-yl)ethanol and 1,3-dioxan-4-ylmethanol was prepared by reaction of 1,2,4-butanetriol with paraformaldehyde. This mixture was subjected to O-alkylation, O-acylation, condensation with phenyl isocyanate, and substitution of OH groups for Cl. The relative activity of acetone derivatives of glycerol and 1,2,4-butanetriol in reactions with allyl chloride and benzyl chloride was estimated.