Methyl 3-(chlorosulfonyl)pyridine-2-carboxylate
CAS No.:
1000887-24-0
M. Wt:
235.64500
M. Fa:
C7H6ClNO4S
InChI Key:
NPGWMJZYBJTPRV-UHFFFAOYSA-N
Names and Identifiers of 1000887-24-0
CAS Number |
1000887-24-0 |
|---|---|
MDL Number |
MFCD19201239 |
IUPAC Name |
methyl 3-chlorosulfonylpyridine-2-carboxylate |
InChI |
InChI=1S/C7H6ClNO4S/c1-13-7(10)6-5(14(8,11)12)3-2-4-9-6/h2-4H,1H3 |
InChIKey |
NPGWMJZYBJTPRV-UHFFFAOYSA-N |
Canonical SMILES |
COC(=O)C1=C(C=CC=N1)S(=O)(=O)Cl |
UNSPSC Code |
12352100 |
Physical and chemical properties of 1000887-24-0
Exact Mass |
234.97100 |
|---|---|
H Bond Acceptors |
4 |
H Bond Donors |
0 |
LogP |
1.87650 |
Molecular Formula |
C7H6ClNO4S |
Molecular Weight |
235.64500 |
PSA |
81.71000 |
Safety Information of 1000887-24-0
Applications of 1000887-24-0
Methyl 3-(chlorosulfonyl)pyridine-2-carboxylate has several applications, particularly in:
- Pharmaceuticals: It serves as an intermediate in the synthesis of biologically active compounds, including potential drug candidates.
- Chemical Synthesis: The compound is utilized as a reagent in organic synthesis, particularly for introducing sulfonamide functionalities into target molecules.
- Agricultural Chemicals: It may find use in developing agrochemicals due to its potential biological activity against pests or pathogens.
Interaction Studies of 1000887-24-0
Interaction studies involving methyl 3-(chlorosulfonyl)pyridine-2-carboxylate are crucial for understanding its reactivity and biological implications. These studies often focus on:
- Reactivity with Biological Molecules: Investigating how this compound interacts with proteins or nucleic acids can reveal potential therapeutic targets.
- Synergistic Effects: Analyzing its interactions with other pharmacologically active compounds may enhance understanding of combinatorial effects in drug formulations.
Such studies are essential for assessing the safety and efficacy of this compound in medicinal chemistry.