structure of 3,5-Diiodo-6-methylpyridin-2-amine

3,5-Diiodo-6-methylpyridin-2-amine

CAS No.: 1000342-88-0
M. Wt: 359.93400
M. Fa: C6H6I2N2
InChI Key: BSXUGYBTSPNQDE-UHFFFAOYSA-N

Names and Identifiers of 3,5-Diiodo-6-methylpyridin-2-amine

CAS Number

1000342-88-0

EC Number

680-945-9

MDL Number

MFCD09880040

IUPAC Name

3,5-diiodo-6-methylpyridin-2-amine

InChI

InChI=1S/C6H6I2N2/c1-3-4(7)2-5(8)6(9)10-3/h2H,1H3,(H2,9,10)

InChIKey

BSXUGYBTSPNQDE-UHFFFAOYSA-N

Canonical SMILES

CC1=NC(=C(C=C1I)I)N

UNSPSC Code

12352100

Physical and chemical properties of 3,5-Diiodo-6-methylpyridin-2-amine

Exact Mass

359.86200

LogP

2.76260

Molecular Formula

C6H6I2N2

Molecular Weight

359.93400

PSA

38.91000

Storage condition

2-8°C

Safety Information of 3,5-Diiodo-6-methylpyridin-2-amine

Pictograms

Signal Word

 Danger

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

Applications of 3,5-Diiodo-6-methylpyridin-2-amine

3,5-Diiodo-6-methylpyridin-2-amine has several applications:

  • Chemistry: Used as a building block for synthesizing more complex pyridine derivatives.
  • Biology: Explored for its potential biological activities, including antimicrobial and anticancer properties.
  • Medicine: Investigated as a precursor for drug development due to its structural features.
  • Industry: Utilized in developing materials with specific electronic properties.

Interaction Studies of 3,5-Diiodo-6-methylpyridin-2-amine

The interactions of 3,5-Diiodo-6-methylpyridin-2-amine with biological targets are crucial for understanding its potential therapeutic effects. Studies suggest that the compound can form stable complexes with enzymes and receptors through halogen bonding facilitated by the iodine atoms. These interactions may enhance the specificity and efficacy of the compound in biological systems, leading to various pharmacological outcomes.

Biological Activity of 3,5-Diiodo-6-methylpyridin-2-amine

Research indicates that 3,5-Diiodo-6-methylpyridin-2-amine may possess significant biological activities. It has been investigated for potential antimicrobial and anticancer properties. The mechanism of action is thought to involve interactions with various molecular targets, such as enzymes and receptors, where the iodine atoms enhance binding affinity through halogen bonding. This characteristic may lead to modulation of biological pathways, thereby exerting therapeutic effects.