structure of Sodium 2,6-dichlorobenzoate

Sodium 2,6-dichlorobenzoate

CAS No.: 10007-84-8
M. Wt: 212.99300
M. Fa: C7H3Cl2NaO2
InChI Key: LZSRENODTOCXKJ-UHFFFAOYSA-M
Appearance: White Solid

Names and Identifiers of Sodium 2,6-dichlorobenzoate

CAS Number

10007-84-8

MDL Number

MFCD03265334

IUPAC Name

sodium;2,6-dichlorobenzoate

InChI

InChI=1S/C7H4Cl2O2.Na/c8-4-2-1-3-5(9)6(4)7(10)11;/h1-3H,(H,10,11);/q;+1/p-1

InChIKey

LZSRENODTOCXKJ-UHFFFAOYSA-M

Canonical SMILES

C1=CC(=C(C(=C1)Cl)C(=O)[O-])Cl.[Na+]

UNSPSC Code

12352100

Physical and chemical properties of Sodium 2,6-dichlorobenzoate

Exact Mass

211.94100

LogP

1.35690

Molecular Formula

C7H3Cl2NaO2

Molecular Weight

212.99300

PSA

40.13000

Storage condition

Inert atmosphere,Room Temperature

Safety Information of Sodium 2,6-dichlorobenzoate

Pictograms

Signal Word

Warning

Safety Data Sheet

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

Applications of Sodium 2,6-dichlorobenzoate

Sodium 2,6-dichlorobenzoate serves multiple purposes in various fields:

  • Intermediate in Organic Synthesis: It is widely used as a building block for synthesizing more complex organic molecules.
  • Agricultural Chemicals: The compound may have applications in developing herbicides or pesticides due to its biological activity.
  • Research: Utilized in biochemical studies to explore enzyme interactions and mechanisms.

Interaction Studies of Sodium 2,6-dichlorobenzoate

Studies on sodium 2,6-dichlorobenzoate often focus on its interactions with enzymes and proteins. The compound's ability to inhibit specific enzymes can be leveraged for research into metabolic pathways and potential therapeutic applications. Its unique structure allows for selective binding to certain biological targets, making it a valuable tool in pharmacological research.

Biological Activity of Sodium 2,6-dichlorobenzoate

Sodium 2,6-dichlorobenzoate exhibits biological activity primarily through enzyme inhibition. It can interact with specific molecular targets, affecting biochemical pathways by binding to active sites of enzymes. The presence of chlorine atoms increases its reactivity and binding affinity, which may lead to potential applications in pharmacology or toxicology.