structure of 1,2-Dibromo-5-fluoro-3-methylbenzene

1,2-Dibromo-5-fluoro-3-methylbenzene

CAS No.: 1000576-64-6
M. Wt: 267.92100
M. Fa: C7H5Br2F
InChI Key: UVWQDDHNMVVFOR-UHFFFAOYSA-N
Appearance: Low Melting Solid

Names and Identifiers of 1,2-Dibromo-5-fluoro-3-methylbenzene

CAS Number

1000576-64-6

MDL Number

MFCD09800773

IUPAC Name

1,2-dibromo-5-fluoro-3-methylbenzene

InChI

InChI=1S/C7H5Br2F/c1-4-2-5(10)3-6(8)7(4)9/h2-3H,1H3

InChIKey

UVWQDDHNMVVFOR-UHFFFAOYSA-N

Canonical SMILES

CC1=CC(=CC(=C1Br)Br)F

UNSPSC Code

12352100

Physical and chemical properties of 1,2-Dibromo-5-fluoro-3-methylbenzene

Exact Mass

265.87400

LogP

3.65910

Molecular Formula

C7H5Br2F

Molecular Weight

267.92100

Safety Information of 1,2-Dibromo-5-fluoro-3-methylbenzene

Pictograms

Signal Word

Warning

Safety Data Sheet

Supports customized editing of SDS information and downloading in PDF documents.

Applications of 1,2-Dibromo-5-fluoro-3-methylbenzene

1,2-Dibromo-5-fluoro-3-methylbenzene has several applications across various fields:

  • Chemical Research: It serves as an intermediate in the synthesis of more complex organic molecules.
  • Pharmaceutical Development: Its derivatives may lead to the creation of new therapeutic agents.
  • Industrial Use: The compound is utilized in producing specialty chemicals and materials.

Interaction Studies of 1,2-Dibromo-5-fluoro-3-methylbenzene

Interaction studies involving 1,2-dibromo-5-fluoro-3-methylbenzene focus on its reactivity with biological molecules. The unique combination of halogens influences its interaction profile with target proteins or enzymes. Research has shown that halogenated compounds can significantly alter binding affinities and specificities due to their ability to form diverse non-covalent interactions.

Similar Compounds

Several compounds share structural similarities with 1,2-dibromo-5-fluoro-3-methylbenzene. Here are some notable examples:

Compound NameStructure Characteristics
1,2-Dibromo-4-fluoro-5-methylbenzeneSimilar structure but different positions of bromine and fluorine atoms.
1,3-Dibromo-5-fluorobenzeneLacks the methyl group; different substitution pattern on the benzene ring.
1-Bromo-3-fluoro-5-(trifluoromethyl)benzeneContains a trifluoromethyl group; different halogen substitution pattern.

Biological Activity of 1,2-Dibromo-5-fluoro-3-methylbenzene

Research indicates that halogenated compounds like 1,2-dibromo-5-fluoro-3-methylbenzene can exhibit significant biological activity. The presence of halogens often enhances the binding affinity and specificity toward biological targets, such as proteins or enzymes. Interaction studies have shown that compounds with halogen substituents can engage in non-covalent interactions, including hydrogen bonding and hydrophobic interactions, which are crucial for their biological efficacy.

Retrosynthesis analysis of 1,2-Dibromo-5-fluoro-3-methylbenzene

  • Route#1

    Cas:202865-77-8
    Cas:1000576-64-6

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