CAS 6305-43-7

1,4-Dibromo-2,3-butanedione

Description:

1,4-Dibromo-2,3-butanedione, with the CAS number 6305-43-7, is an organic compound characterized by its diketone structure, featuring two bromine atoms attached to the 1 and 4 positions of a butanedione backbone. This compound typically appears as a yellow to brown solid and is known for its reactivity due to the presence of the carbonyl groups, which can participate in various chemical reactions, including nucleophilic additions and condensation reactions. Its bromine substituents enhance its electrophilic character, making it useful in synthetic organic chemistry, particularly in the synthesis of more complex molecules. The compound is soluble in organic solvents but has limited solubility in water. Safety considerations are important when handling this substance, as it may pose health risks, including potential toxicity and environmental hazards. Proper laboratory practices should be followed to mitigate exposure. Overall, 1,4-Dibromo-2,3-butanedione serves as a valuable intermediate in chemical synthesis and research applications.

Formula: C₄H₄Br₂O₂

InChI: InChI=1S/C4H4Br2O2/c5-1-3(7)4(8)2-6/h1-2H2

InChI key: InChIKey=RZMOICJDRADLCT-UHFFFAOYSA-N

SMILES: C(C(CBr)=O)(CBr)=O

Synonyms:

• 1,4-Dibromo-2,3-butanedione, (1,4-Dibromodiacetyl)
• 1,4-Dibromobutane-2,3-Dione
• 2,3-Butanedione, 1,4-dibromo-
• NSC 41130
• NSC 75722
• alpha,alpha-Dibromobiacetyl~1,4-Dibromodiacetyl
• 1,4-Dibromo-2,3-butanedione

1,4-DIBROMO-2,3-BUTANEDIONE

CAS: 6305-43-7

Formula: C₄H₄Br₂O₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 243.8814

Ref: IN-DA00E8U6

1,4-Dibromo-2,3-Butanedione

CAS: 6305-43-7

1,4-Dibromo-2,3-Butanedione

Purity: 98%

Molecular weight: 243.88g/mol

Ref: 54-OR1029766

1,4-Dibromo-2,3-butanedione

CAS: 6305-43-7

1,4-Dibromo-2,3-butanedione is an organic compound that is used as a model organism in organic chemistry. It is reactive with light and can emit light when it reacts with oxygen. 1,4-Dibromo-2,3-butanedione has been studied for its use in the synthesis of adenine nucleotides and amino acids. This chemical also has reactive functional groups that can be used to synthesize other molecules. The chlorine atom present in the molecule makes it reactive with many other compounds. 1,4-Dibromo-2,3-butanedione is not found naturally but can be synthesized from dehydroabietic acid through a series of steps involving oxidation and reduction reactions.

Formula: C₄H₄Br₂O₂

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 243.88 g/mol

Ref: 3D-FD163491

1,4-Dibromobutane-2,3-dione

CAS: 6305-43-7

Formula: C₄H₄Br₂O₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 243.882

Ref: 10-F240795