structure of 4,5-Dimethoxypyridin-2-amine

4,5-Dimethoxypyridin-2-amine

CAS No.: 1000843-61-7
M. Wt: 154.167
M. Fa: C7H10N2O2
InChI Key: XKKKEZUQYZLTGG-UHFFFAOYSA-N
Appearance: Light Yellow To Brown Solid

Names and Identifiers of 4,5-Dimethoxypyridin-2-amine

CAS Number

1000843-61-7

MDL Number

MFCD12913799

IUPAC Name

4,5-dimethoxypyridin-2-amine

InChI

InChI=1S/C7H10N2O2/c1-10-5-3-7(8)9-4-6(5)11-2/h3-4H,1-2H3,(H2,8,9)

InChIKey

XKKKEZUQYZLTGG-UHFFFAOYSA-N

Canonical SMILES

COC1=CC(=NC=C1OC)N

UNSPSC Code

12352100

Physical and chemical properties of 4,5-Dimethoxypyridin-2-amine

Acidity coefficient

4.57±0.10(Predicted)

Boiling Point

282.4±35.0 °C at 760 mmHg

Density

1.2±0.1 g/cm3

Exact Mass

154.074234

Flash Point

124.6±25.9 °C

Index of Refraction

1.544

LogP

1.02

Molecular Formula

C7H10N2O2

Molecular Weight

154.167

PSA

58.10000

Storage condition

2-8°C(protect from light)

Vapour Pressure

0.0±0.6 mmHg at 25°C

Safety Information of 4,5-Dimethoxypyridin-2-amine

Pictograms

Signal Word

 Warning

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

Applications of 4,5-Dimethoxypyridin-2-amine

4,5-Dimethoxypyridin-2-amine has a wide range of applications:

  • Medicinal Chemistry: It is explored for its potential as a building block in drug development, particularly for enzyme inhibitors.
  • Coordination Chemistry: Serves as a ligand due to its ability to coordinate with metal ions.
  • Industrial Uses: Utilized in the production of dyes, pigments, and other industrial chemicals.

Interaction Studies of 4,5-Dimethoxypyridin-2-amine

Studies on the interactions of 4,5-Dimethoxypyridin-2-amine with biological targets are ongoing. Its ability to act as an enzyme inhibitor suggests that it may interact with specific enzymes involved in metabolic pathways or disease processes. Further research is necessary to elucidate these interactions fully.

Biological Activity of 4,5-Dimethoxypyridin-2-amine

Research indicates that 4,5-Dimethoxypyridin-2-amine exhibits notable biological activities. Preliminary studies suggest potential antimicrobial and anticancer properties, making it a candidate for further investigation in drug development. Its structural similarity to other biologically active compounds may contribute to its efficacy as an enzyme inhibitor.