structure of 5-Bromo-2-methyl-4-methylsulfonylphenylhydrazine

5-Bromo-2-methyl-4-methylsulfonylphenylhydrazine

CAS No.: 1000018-33-6
M. Wt: 279.15400
M. Fa: C8H11BrN2O2S
InChI Key: ILCXSEHPOZCVAQ-UHFFFAOYSA-N
Appearance: Solid

Names and Identifiers of 1000018-33-6

CAS Number

1000018-33-6

MDL Number

MFCD09264558

IUPAC Name

(5-bromo-2-methyl-4-methylsulfonylphenyl)hydrazine

InChI

InChI=1S/C8H11BrN2O2S/c1-5-3-8(14(2,12)13)6(9)4-7(5)11-10/h3-4,11H,10H2,1-2H3

InChIKey

ILCXSEHPOZCVAQ-UHFFFAOYSA-N

Canonical SMILES

CC1=CC(=C(C=C1NN)Br)S(=O)(=O)C

UNSPSC Code

12352100

Physical and chemical properties of 1000018-33-6

Exact Mass

277.97200

LogP

3.30070

Melting Point

195 to 197°C

Molecular Formula

C8H11BrN2O2S

Molecular Weight

279.15400

PSA

80.57000

Safety Information of 1000018-33-6

Pictograms

Signal Word

 Warning

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

Applications of 1000018-33-6

5-Bromo-2-methyl-4-methylsulfonylphenylhydrazine finds applications in:

  • Proteomics Research: Due to its ability to modify proteins and peptides, it is used as a biochemical tool for studying protein interactions and functions.
  • Medicinal Chemistry: The compound serves as a lead structure for developing new pharmaceuticals targeting specific diseases.
  • Organic Synthesis: It acts as an intermediate in the synthesis of more complex organic molecules.

These applications underscore its significance in both academic research and industrial settings.

Interaction Studies of 1000018-33-6

Interaction studies involving 5-Bromo-2-methyl-4-methylsulfonylphenylhydrazine focus on its binding affinity to various biological molecules. Preliminary studies indicate that it may interact with enzymes or receptors, potentially modulating their activity. Further investigations using techniques such as surface plasmon resonance (SPR) or enzyme-linked immunosorbent assays (ELISA) are necessary to quantify these interactions and understand their implications in biological systems.

Biological Activity of 1000018-33-6

Research indicates that 5-Bromo-2-methyl-4-methylsulfonylphenylhydrazine exhibits various biological activities, particularly as an inhibitor of certain enzymes involved in metabolic pathways. Its structural features may contribute to its interaction with biological targets, making it a candidate for further investigation in drug development. Studies have suggested potential anti-inflammatory and anti-cancer properties, although more research is needed to fully elucidate its mechanisms of action and therapeutic potential.