3580-97-0 Usage
Uses
Used in Pharmaceutical Synthesis:
3-bromo-2,2-bis(bromomethyl)propyl acetate is employed as an intermediate in the production of various pharmaceuticals. Its unique chemical structure allows for the creation of a range of medicinal compounds, contributing to the development of new treatments and therapies.
Used in Agrochemical Production:
In the agrochemical industry, 3-bromo-2,2-bis(bromomethyl)propyl acetate is used as a key intermediate for the synthesis of various agrochemicals. Its role in this sector is crucial for the development of effective pesticides and other agricultural products that protect crops and enhance agricultural productivity.
Used as a Solvent:
3-bromo-2,2-bis(bromomethyl)propyl acetate also serves as a solvent in certain chemical processes. Its properties make it suitable for dissolving specific substances, facilitating reactions, and aiding in the separation or purification of compounds.
Used as a Reagent in Organic Synthesis:
In organic synthesis, 3-bromo-2,2-bis(bromomethyl)propyl acetate is utilized as a reagent. It participates in various chemical reactions, enabling the formation of new compounds and contributing to the advancement of organic chemistry and its applications.
Safety Precautions:
Given its harmful nature if swallowed, inhaled, or absorbed through the skin, 3-bromo-2,2-bis(bromomethyl)propyl acetate must be handled with caution. Trained professionals should use appropriate safety equipment and follow established procedures to minimize risks and ensure safe operations in the laboratory or industrial settings.
Check Digit Verification of cas no
The CAS Registry Mumber 3580-97-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,8 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3580-97:
(6*3)+(5*5)+(4*8)+(3*0)+(2*9)+(1*7)=100
100 % 10 = 0
So 3580-97-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H11Br3O2/c1-6(11)12-5-7(2-8,3-9)4-10/h2-5H2,1H3
3580-97-0Relevant academic research and scientific papers
Synthesis and copolymerization of azidomethyl-substituted oxetanes: the morphology of statistical block copolymers
Mukhametshin, Timur I.,Petrov, Aleksei I.,Kuznetsova, Nina V.,Petrov, Vladimir A.,Averianova, Natalia V.,Garaev, Ilgiz Kh.,Kostochko, Anatoly V.,Gubaidullin, Aidar T.,Vinogradov, Dmitry B.,Bulatov, Pavel V.
, p. 811 - 821 (2017/09/06)
[Figure not available: see fulltext.] 3,3-Bis(azidomethyl)oxetane and 3-azidomethyl-3-methyloxetane were obtained by bromination of pentaerythritol and metriol with a mixture of hydrobromic, acetic, and sulfuric acids, followed by cyclization in the presence of a phase-transfer catalyst TBAB, with the formation of oxetane ring and replacement of bromide substituents with azide ions. The copolymerization reaction of 3,3-bis-(azidomethyl)oxetane and 3-azidomethyl-3-methyloxetane was performed in the presence of a catalytic system prepared from triisobutylaluminum and water. The methods of small-angle and wide-angle X-ray diffraction analysis were used to determine the amorphous-crystalline and domain structures of the synthesized copolymers. We also present data about conformational and relaxation transitions in these statistical copolymers.
