1,2-Dibromobutane | 533-98-2

Additional information

CAS ID

533-98-2

IUPAC Name

1,2-dibromobutane

Molecular Formula

C4H8Br2

Molecular Weight

SMILES

CCC(Br)CBr

General Information

Additional information

CAS ID

533-98-2

IUPAC Name

1,2-dibromobutane

Molecular Formula

C4H8Br2

Molecular Weight

SMILES

CCC(Br)CBr

Description

10792

Synonym : butane, 1,2-dibromo, .alpha.-butylene dibromide, alpha-butylene dibromide, 1,2-dibomobutane, 1,2 dibromobutane, butane,2-dibromo, 1,2-dibromo-butane, alpha-butylene bromide, 1,2-butylene bromide, .alpha.-butylene bromide

Color Yellow
Boiling Point 166°C
Formula Weight 215.92
Physical Form Clear Liquid at 20°C
Chemical Name or Material 1,2-Dibromobutane

technical service

Our scientists have experience in all research areas, including life science, material science, chemical custom synthesis, chromatography, analytical science, and many others.

1,2-Dibromobutane | 533-98-2 FAQS

1,2-Dibromobutane has the formula C4H8Br2. It has four carbon atoms, eight hydrogen atoms, and two bromine atoms. The bromine atoms are connected to nearby carbon atoms, which makes them reactive in different chemical uses.

The 1,2-dibromobutane structure has a four-carbon backbone with bromine atoms on adjacent carbons. This arrangement improves its utility in synthesis, enabling halogen substitution and elimination reactions essential for producing complex organic compounds in industrial applications.

1,2-dibromobutane melting point is -65°C. The presence of bromine atoms affects its physical effects, changing how it moves between different states and how easily it dissolves in different chemicals.

1,2-Dibromobutane is used in organic synthesis, acting as an intermediate for pharmaceuticals, agrochemicals, and specialized polymers. Its bromine structure helps it add distinct groups during chemical changes.

1,2-Dibromobutane is made by adding bromine to butene or its related compounds using specific ways to control the reaction. Adding bromine carefully creates a product with a clear reaction, making it useful for both industry and lab work.