37167-59-2 Usage
Uses
Used in Organic Synthesis:
DIMETHYL DIBROMOMALONATE is used as a reagent for the preparation of various organic compounds, leveraging its high reactivity to facilitate the synthesis process.
Used in Pharmaceutical Synthesis:
DIMETHYL DIBROMOMALONATE is used as a versatile intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs and medicines.
Used in Agrochemical Production:
DIMETHYL DIBROMOMALONATE is utilized in the synthesis of agrochemicals, playing a role in the creation of substances that protect crops and enhance agricultural productivity.
Used in Fine Chemicals Synthesis:
DIMETHYL DIBROMOMALONATE is employed as an intermediate in the production of other fine chemicals, which are high-purity, high-value chemicals used in various industries.
Used in Polymer Production:
DIMETHYL DIBROMOMALONATE is used as a reactant in the manufacturing of polymers, contributing to the formation of materials with specific properties for use in various applications.
Used in Industrial Product Manufacturing:
DIMETHYL DIBROMOMALONATE is incorporated into the production of other industrial products, highlighting its broad applicability across different sectors.
Check Digit Verification of cas no
The CAS Registry Mumber 37167-59-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,1,6 and 7 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 37167-59:
(7*3)+(6*7)+(5*1)+(4*6)+(3*7)+(2*5)+(1*9)=132
132 % 10 = 2
So 37167-59-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H6Br2O4/c1-10-3(8)5(6,7)4(9)11-2/h1-2H3
37167-59-2Relevant academic research and scientific papers
Lipophilic indole mediated chemoselective α-monobromination of 1,3-dicarbonyl compounds
Wong, Jonathan,Ke, Zhihai,Yeung, Ying-Yeung
, (2020/03/04)
A mild and efficient mono-selective bromination of 1,3-dicarbonyl compounds has been developed using lipophilic indole catalysts. Inexpensive and commercially available N-bromosuccinimide (NBS) was used as the brominating reagent. The selectivity was further enhanced when using stoichiometric amount of 3-bromoindole species. Mechanistic studies reveal that the indole catalyst has dual functions in the mono-bromination process.
