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(+/-)-alpha-bromo-alpha-methyl-gamma-butyrolactone, also known as alpha-bromo-alpha-methyl-gamma-butyrolactone or BMGBL, is a chiral lactone compound with the molecular formula C6H9BrO2. As a racemic mixture, it contains both the (+) and (-) enantiomers, making it a valuable building block in organic chemistry due to its reactivity as a halogenated lactone.

122040-92-0

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122040-92-0 Usage

Uses

Used in Organic Synthesis:
(+/-)-alpha-bromo-alpha-methyl-gamma-butyrolactone is used as a key intermediate in the synthesis of various biologically active compounds, contributing to the development of new pharmaceuticals and agrochemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (+/-)-alpha-bromo-alpha-methyl-gamma-butyrolactone serves as a precursor for the preparation of drugs, playing a crucial role in the discovery and production of novel therapeutic agents.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, (+/-)-alpha-bromo-alpha-methyl-gamma-butyrolactone is utilized as a starting material for the creation of new pesticides and other agricultural chemicals, enhancing crop protection and yield.

Check Digit Verification of cas no

The CAS Registry Mumber 122040-92-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,0,4 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 122040-92:
(8*1)+(7*2)+(6*2)+(5*0)+(4*4)+(3*0)+(2*9)+(1*2)=70
70 % 10 = 0
So 122040-92-0 is a valid CAS Registry Number.

122040-92-0Relevant academic research and scientific papers

A useful synthesis of 3-methyl-2(5H)-furanone

Cruz-Almanza,Padilla Higareda

, p. 1097 - 1104 (1991)

An efficient procedure for the preparation of furanone 3 from commercially available starting material lactone 1, is reported.

Preparation of α-Hydroxy-γ-lactones and their Application in the Synthesis of α,β-Butenolides, α-Alkylidene-γ-lactones and Furans

Munoz, A. Heber,Tamariz, Joaquin,Jimenez, Rogelio,Mora, Gustavo Garcia de la

, p. 501 - 522 (2007/10/02)

A straightforward synthesis of α-hydroxy-γ-butyrolactones was carried out by condensation reaction of the lithium anion of ethoxyethyl-protected cyanohydrins with epoxides, followed by acidic treatment.Synthetic applications of these synthons in the preparation of interesting α,β-butenolides, α-alkylidene-γ-lactones and furans are described.

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