structure of 4-(chlorosulfonyl)-1-methyl-1H-pyrrole-2-carboxylic acid

4-(chlorosulfonyl)-1-methyl-1H-pyrrole-2-carboxylic acid

CAS No.: 1000932-01-3
M. Wt: 223.63
M. Fa: C6H6ClNO4S
InChI Key: POMZQIUIOJIHIN-UHFFFAOYSA-N

Names and Identifiers of 1000932-01-3

CAS Number

1000932-01-3

EC Number

848-519-9

MDL Number

MFCD09863423

IUPAC Name

4-chlorosulfonyl-1-methylpyrrole-2-carboxylic acid

InChI

InChI=1S/C6H6ClNO4S/c1-8-3-4(13(7,11)12)2-5(8)6(9)10/h2-3H,1H3,(H,9,10)

InChIKey

POMZQIUIOJIHIN-UHFFFAOYSA-N

Canonical SMILES

CN1C=C(C=C1C(=O)O)S(=O)(=O)Cl

UNSPSC Code

12352100

Physical and chemical properties of 1000932-01-3

Acidity coefficient

3.10±0.41(Predicted)

Boiling Point

426.4±30.0 °C(Predicted)

Density

1.65±0.1 g/cm3(Predicted)

Molecular Formula

C6H6ClNO4S

Molecular Weight

223.63

Safety Information of 1000932-01-3

Pictograms

Signal Word

 Danger

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

Applications of 1000932-01-3

4-(Chlorosulfonyl)-1-methyl-1H-pyrrole-2-carboxylic acid finds applications primarily in polymer chemistry and catalysis:

  • Polymer Chemistry: It serves as a chemical reagent in catalyzing living radical polymerizations, enabling controlled growth of polymer chains with specific properties.
  • Catalysis: The compound is also utilized in preparing polymer-bound transfer hydrogenation catalysts, which are useful in various organic transformations.

Biological Activity of 1000932-01-3

Currently, there is insufficient scientific research available to definitively characterize the biological activity of 4-(chlorosulfonyl)-1-methyl-1H-pyrrole-2-carboxylic acid. While its structural components suggest potential biological interactions, particularly due to the reactive nature of the chlorosulfonyl group, no comprehensive studies have documented its mechanism of action or specific biological effects within living systems.