3492-43-1 Usage
Description
[2-(acetyloxymethyl)-3-bromo-2-(bromomethyl)propyl] acetate is a chemical compound characterized by its molecular formula C8H12Br2O4. It is a combined ester of acetyloxymethyl and acetate, featuring bromomethyl and bromine atoms within its structure. [2-(acetyloxymethyl)-3-bromo-2-(bromomethyl)propyl] acetate is known for its reactivity in various chemical reactions and its application in the synthesis of other organic compounds, as well as its use in the pharmaceutical industry for drug production.
Uses
Used in Chemical Synthesis:
[2-(acetyloxymethyl)-3-bromo-2-(bromomethyl)propyl] acetate is used as a reagent in chemical synthesis for the creation of other organic compounds. Its unique structure, which includes bromine and bromomethyl groups, allows for versatile reactions and the formation of a wide range of products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, [2-(acetyloxymethyl)-3-bromo-2-(bromomethyl)propyl] acetate is utilized as a key component in the production of certain drugs. Its presence in the molecular structure of these drugs contributes to their therapeutic properties and effectiveness.
Used in Research and Development:
Due to its reactivity and structural features, [2-(acetyloxymethyl)-3-bromo-2-(bromomethyl)propyl] acetate is also employed in research and development settings. Scientists and chemists use this compound to explore new reaction pathways, develop novel chemical processes, and create innovative materials with potential applications in various industries.
Safety Considerations:
The presence of bromine in the molecule makes [2-(acetyloxymethyl)-3-bromo-2-(bromomethyl)propyl] acetate potentially hazardous. As a result, it requires careful handling and storage to ensure the safety of those working with it. Proper safety protocols and equipment should be in place to minimize the risk of exposure and accidents.
Check Digit Verification of cas no
The CAS Registry Mumber 3492-43-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,9 and 2 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3492-43:
(6*3)+(5*4)+(4*9)+(3*2)+(2*4)+(1*3)=91
91 % 10 = 1
So 3492-43-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H14Br2O4/c1-7(12)14-5-9(3-10,4-11)6-15-8(2)13/h3-6H2,1-2H3
3492-43-1Relevant articles and documents
Synthesis of 2-bromomethyl-3-hydroxy-2-hydroxymethyl-propyl pyrimidine and theophylline nucleosides under microwave irradiation. Evaluation of their activity against hepatitis B virus
Ashry,Rashed,Abdel-Rahman,Awad,Rasheed
, p. 925 - 939 (2008/02/08)
Alkylation of 2-methylthiopyrimidin-4(1H)-one (1a) and its 5(6)-alkyl derivatives 1b - d as well as theophylline (7) with 2,2- bis (bromomethyl)-1,3-diacetoxypropane (2) under microwave irradia-tion gave the corresponding acyclonucleosides 1-[(3-acetoxy-2-acetoxymethyl-2-bromomethyl) prop-1- yl ]-2-methyl-thio pyrmidin-4(1H)-ones 3a - d and 7-[(3-acetoxy-2- acetoxymethyl-2-bromomethyl)prop-1- yl]theophylline (8), which upon further irradiation gave the double-headed acyclonucleosides 1,1 ′-[(2,2- diacetoxymethyl)-1,3-propylidene]- bis [(2-(methylthio)-pyrimidin-4(1H)-ones] 4a - c , and 7,7 ′-[(2,2-diacetoxymethyl)-1,3-propylidene]- bis (theophylline) (9). The deacetylated derivatives were obtained by the action of sodium methoxide. The activity of deacetylated nucleosides against Hepatitis B virus was evaluated. Compound 5b showed moderate inhibition activity against HBV with mild cytotoxicity. Copyright Taylor & Francis Group, LLC.