(2-Methyl-1,3-thiazol-4-yl)methanesulfonyl chloride
CAS No.:
1000394-87-5
M. Wt:
211.69000
M. Fa:
C5H6ClNO2S2
InChI Key:
IJAYMUFRRBWQPU-UHFFFAOYSA-N
Names and Identifiers of 1000394-87-5
CAS Number |
1000394-87-5 |
|---|---|
EC Number |
830-798-3 |
MDL Number |
MFCD16671829 |
IUPAC Name |
(2-methyl-1,3-thiazol-4-yl)methanesulfonyl chloride |
InChI |
InChI=1S/C5H6ClNO2S2/c1-4-7-5(2-10-4)3-11(6,8)9/h2H,3H2,1H3 |
InChIKey |
IJAYMUFRRBWQPU-UHFFFAOYSA-N |
Canonical SMILES |
CC1=NC(=CS1)CS(=O)(=O)Cl |
UNSPSC Code |
12352100 |
Physical and chemical properties of 1000394-87-5
Exact Mass |
210.95300 |
|---|---|
H Bond Acceptors |
3 |
H Bond Donors |
0 |
LogP |
2.60090 |
Molecular Formula |
C5H6ClNO2S2 |
Molecular Weight |
211.69000 |
PSA |
83.65000 |
Safety Information of 1000394-87-5
Applications of 1000394-87-5
The applications of (2-Methyl-1,3-thiazol-4-yl)methanesulfonyl chloride are diverse:
- Synthetic Intermediates: It serves as a versatile intermediate in the synthesis of pharmaceuticals and agrochemicals.
- Bioconjugation: The reactive sulfonyl chloride group can be utilized for bioconjugation processes in drug development.
- Research Reagent: Used in laboratory settings for various organic synthesis applications due to its electrophilic nature.
Interaction Studies of 1000394-87-5
Interaction studies involving (2-Methyl-1,3-thiazol-4-yl)methanesulfonyl chloride focus on its reactivity with different nucleophiles and potential biological targets. These studies help elucidate its mechanism of action and potential therapeutic applications. For instance, investigations into its interaction with amino acids or peptides could provide insights into its utility as a modifying agent in peptide synthesis or drug design.
Cas:39238-07-8
