3580-97-0

Basic information

• Product Name: 3-broMo-2,2-bis(broMoMethyl)propyl acetate
• Synonyms: 3-broMo-2,2-bis(broMoMethyl)propyl acetate
• CAS NO: 3580-97-0
• Molecular Formula: C₇H₁₁Br₃O₂
• Molecular Weight: 366.87304
• Mol File: 3580-97-0.mol
• Article Data: 1

Chemical Properties

• Melting Point: 42-43 °C
• Boiling Point: 351.1°Cat760mmHg
• Flash Point: 166.2°C
• Appearance: /
• Density: 1.96g/cm³
• Vapor Pressure: 4.19E-05mmHg at 25°C
• Refractive Index: 1.547
• CAS DataBase Reference: 3-broMo-2,2-bis(broMoMethyl)propyl acetate(CAS DataBase Reference)
• NIST Chemistry Reference: 3-broMo-2,2-bis(broMoMethyl)propyl acetate(3580-97-0)
• EPA Substance Registry System: 3-broMo-2,2-bis(broMoMethyl)propyl acetate(3580-97-0)

Safety Data

• Hazardous Substances Data: 3580-97-0(Hazardous Substances Data)

Usage

General Description

3-bromo-2,2-bis(bromomethyl)propyl acetate is a chemical compound with the molecular formula C8H13Br3O2. It is a colorless liquid with a molecular weight of 312.904 g/mol. This chemical is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It is also used as a solvent and as a reagent in organic synthesis. 3-bromo-2,2-bis(bromomethyl)propyl acetate is known to be harmful if swallowed, inhaled, or absorbed through the skin, and it should be handled with caution by trained professionals using appropriate safety equipment and procedures.

InChI:InChI=1/C7H11Br3O2/c1-6(11)12-5-7(2-8,3-9)4-10/h2-5H2,1H3

Upstream product

• 115-77-5 Pentaerythritol 
• 64-19-7 acetic acid 

Downstream Products

• 2402-83-7 3,3-bis(bromomethyl)oxetane 
• 13595-48-7 2,6-bis-(toluene-4-sulfonyl)-2,6-diaza-spiro[3.3]heptane 
• 854403-48-8 2-(toluene-4-sulfonylamino)-1,1-bis-[(toluene-4-sulfonylamino)-methyl]-cyclopropane 
• 152922-71-9 1-(hydroxymethyl)cyclopropaneacetonitrile 
• 1522-92-5 2,2-bis(bromomethyl)-3-bromo-propan-1-ol 
• 100119-07-1 benzoic acid-(3-bromo-2,2-bis-bromomethyl-propyl ester) 

Relevant articles and documents

Synthesis and copolymerization of azidomethyl-substituted oxetanes: the morphology of statistical block copolymers

[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.