25966-39-6 Usage
Description
ALPHA-BROMO-GAMMA-VALEROLACTONE is an organic compound that serves as an important intermediate in the synthesis of various chemical compounds. It is characterized by its unique chemical structure, which includes a bromo and a valerolactone group, making it a versatile building block in organic chemistry.
Uses
Used in Chemical Synthesis:
ALPHA-BROMO-GAMMA-VALEROLACTONE is used as a synthetic intermediate for the production of various chemical compounds. Its unique structure allows for further functionalization and modification, making it a valuable component in the synthesis of complex molecules.
Used in Pharmaceutical Industry:
ALPHA-BROMO-GAMMA-VALEROLACTONE is used as a key component in the synthesis of pharmaceutical compounds. Its ability to be modified and functionalized makes it a promising candidate for the development of new drugs with potential therapeutic applications.
Used in the Synthesis of α-(2-ethoxythiocarbonylthio)-γ-valerolactone:
ALPHA-BROMO-GAMMA-VALEROLACTONE is used as a starting material for the synthesis of α-(2-ethoxythiocarbonylthio)-γ-valerolactone, a compound with potential applications in various fields, including pharmaceuticals and materials science. The versatility of ALPHA-BROMO-GAMMA-VALEROLACTONE enables the creation of new compounds with specific properties and functions.
Check Digit Verification of cas no
The CAS Registry Mumber 25966-39-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,9,6 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 25966-39:
(7*2)+(6*5)+(5*9)+(4*6)+(3*6)+(2*3)+(1*9)=146
146 % 10 = 6
So 25966-39-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H7BrO2/c1-3-2-4(6)5(7)8-3/h3-4H,2H2,1H3
25966-39-6Relevant articles and documents
Base-catalyzed ethanolysis of α-diethoxyphosphoryl-γ-lactones: A facile synthesis of cyclopropanecarboxylates
Krawczyk, Henryk,Wa?sek, Katarzyna,K?dzia, Jacek
, p. 2648 - 2652 (2007/10/03)
A range of alkyl- and alkenylcyclopropanecarboxylic acid ethyl esters has been stereoselectively prepared by treatment of substituted α- diethoxyphosphoryl-γ-lactones with sodium ethoxide in tetrahydrofuran. Georg Thieme Verlag Stuttgart.
