CAS 1003-20-9

2,2-Bis(chloromethyl)oxirane

Description:

2,2-Bis(chloromethyl)oxirane, also known as bis(chloromethyl)epoxide, is a chemical compound characterized by its epoxide functional group and two chloromethyl substituents. It is a colorless to pale yellow liquid with a distinctive odor and is known for its reactivity, particularly in nucleophilic substitution reactions due to the presence of the epoxide ring. The compound is classified as a potential carcinogen and poses health risks upon exposure, necessitating careful handling and appropriate safety measures. It is soluble in organic solvents but has limited solubility in water. 2,2-Bis(chloromethyl)oxirane is primarily used in the synthesis of various polymers and as an intermediate in organic synthesis, particularly in the production of chlorinated compounds. Its reactivity allows it to participate in cross-linking reactions, making it valuable in the development of coatings and adhesives. Due to its hazardous nature, it is subject to strict regulatory controls in many jurisdictions.

Formula: C₄H₆Cl₂O

InChI: InChI=1S/C4H6Cl2O/c5-1-4(2-6)3-7-4/h1-3H2

InChI key: InChIKey=QYMBUGYOVSCZTI-UHFFFAOYSA-N

SMILES: C(Cl)C1(CCl)CO1

Synonyms:

• Propane, 1-chloro-2-(chloromethyl)-2,3-epoxy-
• 1-Chloro-2,3-epoxy-2-chloromethylpropane
• Oxirane, 2,2-bis(chloromethyl)-
• 2,2-Bis(chloromethyl)oxirane

OXIRANE, 2,2-BIS(CHLOROMETHYL)-

CAS: 1003-20-9

Formula: C₄H₆Cl₂O

Purity: 97%

Molecular weight: 140.9958

Ref: IN-DA0001HP

2,2-Bis(chloromethyl)oxirane

CAS: 1003-20-9

2,2-Bis(chloromethyl)oxirane

Purity: 97%

Ref: 54-OR1039500

2,2-Bis(chloromethyl)oxirane

CAS: 1003-20-9

Purity: 97%

Molecular weight: 139.98

Ref: 10-F567446

2,2-Bis(chloromethyl)oxirane

CAS: 1003-20-9

2,2-Bis(chloromethyl)oxirane is a chemical intermediate that can be used as a binder in the production of polyurethane and polyester resins. It can also be used to produce target products such as hydroxyethyl acrylate, methacrylic acid, and acrylic acid esters. 2,2-Bis(chloromethyl)oxirane is usually prepared by reacting methylene chloride with chloromethyl methyl ether in the presence of a catalyst such as tetrabutylammonium. The reaction mixture is heated to reflux for at least one hour before cooling to room temperature and adding an excess of water to quench the reaction.

Formula: C₄H₆Cl₂O

Purity: Min. 95%

Molecular weight: 140.99 g/mol

Ref: 3D-BAA00320