structure of (2R)-2-(dimethylamino)propane-1-thiol

(2R)-2-(dimethylamino)propane-1-thiol

CAS No.: 1807938-37-9
M. Wt: 119.23
M. Fa: C5H13NS
InChI Key: -

Names and Identifiers of (2R)-2-(dimethylamino)propane-1-thiol

CAS Number

1807938-37-9

IUPAC Name

(2R)-2-(dimethylamino)propane-1-thiol

Canonical SMILES

C[C@H](CS)N(C)C

Physical and chemical properties of (2R)-2-(dimethylamino)propane-1-thiol

Acidity coefficient

9.99±0.10(Predicted)

Boiling Point

135.4±23.0 °C(Predicted)

Density

0.898±0.06 g/cm3(Predicted)

Molecular Formula

C5H13NS

Molecular Weight

119.23

Applications of (2R)-2-(dimethylamino)propane-1-thiol

(2R)-2-(dimethylamino)propane-1-thiol has several applications across different fields:

  • Chemical Industry: Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals.
  • Material Science: Employed in the development of polymer additives and stabilizers due to its reactivity.
  • Biochemistry: Investigated for its potential role in drug design and development due to its biological activity.

Interaction Studies of (2R)-2-(dimethylamino)propane-1-thiol

Studies on (2R)-2-(dimethylamino)propane-1-thiol focus on its interactions with various biological systems:

  • Protein Binding: Research has shown that thiols can form reversible bonds with cysteine residues in proteins, influencing protein function and stability.
  • Cellular Uptake: Investigations into how this compound enters cells reveal potential pathways for therapeutic delivery.

These studies contribute to understanding how (2R)-2-(dimethylamino)propane-1-thiol might be utilized in medicinal chemistry.

Biological Activity of (2R)-2-(dimethylamino)propane-1-thiol

(2R)-2-(dimethylamino)propane-1-thiol exhibits notable biological activities. Compounds containing thiol groups are often involved in biological processes such as:

  • Antioxidant Activity: Thiols can scavenge free radicals, contributing to cellular protection against oxidative stress.
  • Enzyme Interactions: The compound may interact with various enzymes through thiol-disulfide exchange mechanisms, potentially influencing metabolic pathways.

Research indicates that compounds with similar structures can exhibit neuroprotective effects and may be investigated for their potential therapeutic applications.