83953-42-8 Usage
Description
4-BROMOFURAN-2-CARBOXALDEHYDE ETHYLENE GLYCOL ACETAL is a chemical compound that is commonly used as a reactant in organic synthesis. It is a derivative of furan, a heterocyclic compound, and contains a bromine atom as well as an aldehyde group. The presence of the ethylene glycol acetal group makes this compound a useful building block for the synthesis of various biologically active molecules and pharmaceuticals.
Used in Pharmaceutical Industry:
4-BROMOFURAN-2-CARBOXALDEHYDE ETHYLENE GLYCOL ACETAL is used as a building block for the synthesis of various biologically active molecules and pharmaceuticals due to its unique structure and reactivity.
Used in Fine Chemicals Production:
4-BROMOFURAN-2-CARBOXALDEHYDE ETHYLENE GLYCOL ACETAL is used as a reagent in the production of fine chemicals and agrochemicals, contributing to the development of new and improved products.
Used in Material Science:
4-BROMOFURAN-2-CARBOXALDEHYDE ETHYLENE GLYCOL ACETAL has potential applications in material science due to its unique structure and reactivity, which can be utilized to create new materials with specific properties.
Used in Polymer Chemistry:
4-BROMOFURAN-2-CARBOXALDEHYDE ETHYLENE GLYCOL ACETAL also has potential applications in polymer chemistry, where it can be used to develop new polymers with unique characteristics and functions.
Check Digit Verification of cas no
The CAS Registry Mumber 83953-42-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,9,5 and 3 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 83953-42:
(7*8)+(6*3)+(5*9)+(4*5)+(3*3)+(2*4)+(1*2)=158
158 % 10 = 8
So 83953-42-8 is a valid CAS Registry Number.
83953-42-8Relevant articles and documents
A selective synthesis of 4-bromo-2-furancarboxaldehyde and its pinacolborane derivative
Ilovich, Ohad,Deutsch, Joseph
, p. 1409 - 1411 (2007/10/03)
A selective synthesis of ethylene acetal of 4-bromo-2-furancarboxaldehyde (4) and its pinacolborane derivative (5) is described. The synthesis was carried out using 2-furancarboxaldehyde (1) that was brominated to 4,5-dibromo-2- furancarboxaldehyde (2) in an emulsion of aluminum chloride and methylene chloride. The product was isolated, protected as ethylene acetal, and selectively debrominated to the ethylene acetal of 4-bromo-2-furancarboxaldehyde (4) in one step. This moiety was reacted with pinacolborane to give a reactive reagent of Suzuki coupling.
