2,4-Thiazolidinedione

CAS Number: 2295-31-0

Molecular Formula: C3H3NO2S

Purity: 2,4-Thiazolidinedione 98% purity

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About 2,4-Thiazolidinedione

2,4-Thiazolidinedione (CAS 2295-31-0) is a pivotal heterocyclic building block in the API intermediates market, primarily utilized for the synthesis of glitazone-class antidiabetic agents and novel oncology therapeutics where high purity fine chemicals (Pharma/API purity 99% | General Industry purity 98%) are required ...

2,4-Thiazolidinedione Specifications

CAS Number

2295-31-0

Molecular Formula

C3H3NO2S

Molecular Weight

117.12 g/mol

IUPAC Name

1,3-thiazolidine-2,4-dione

Canonical SMILES

C1C(=O)NC(=O)S1

InChI Key

ZOBPZXTWZATXDG-UHFFFAOYSA-N

InChI

InChI=1S/C3H3NO2S/c5-2-1-7-3(6)4-2/h1H2,(H,4,5,6)

EINECS Number

218-941-2

MDL Number

MFCD00005478

HSN No

29341000

CAS Number

2295-31-0

Molecular Formula

C3H3NO2S

Molecular Weight

117.12 g/mol

IUPAC Name

1,3-thiazolidine-2,4-dione

Canonical SMILES

C1C(=O)NC(=O)S1

InChI Key

ZOBPZXTWZATXDG-UHFFFAOYSA-N

InChI

InChI=1S/C3H3NO2S/c5-2-1-7-3(6)4-2/h1H2,(H,4,5,6)

EINECS Number

218-941-2

MDL Number

MFCD00005478

HSN No

29341000

Molecular Weight

117.12 g/mol

Purity

2,4-Thiazolidinedione 98% purity

Melting Point

124.0 to 128.0 °C

Boiling Point

178-179 °C (19 mmHg)

Freezing point

123-125 °C

Flash Point

138 °C

Density

1.408 (estimate)

pKa

6.50±0.10

Precise Quality

2295-31-0

PSA

45.2 Å²

logP

-0.29

Average mass

117.13 g/mol

Monoisotopic mass

116.98844951 Da

Molar mass

117.13 g/mol

Vapour pressure

0 Pa at 25 °C

Precautionary Statement Codes

P261, P264+P265, P272, P280, P302+P352, P305+P351+P338, P321, P333+P317, P337+P317, P362+P364, and P501

Hazard Classes and Categories

Skin Sens. 1 (96.4%) Eye Irrit. 2A (100%)

Pharmaceutical Intermediate

A versatile scaffold and key building block used in the synthesis of various bioactive derivatives and active pharmaceutical ingredients, including FDA-approved glitazones like pioglitazone and rosiglitazone

Antidiabetic Agent

A primary therapeutic pharmacophore that acts as a PPAR-gamma agonist to increase insulin sensitivity, enhance glucose uptake, and manage type 2 diabetes mellitus

Organic Synthesis Building Block

A privileged sulfur-containing heterocyclic motif utilized in medicinal chemistry research to develop compounds with antimicrobial, anticancer, anti-inflammatory, and antioxidant activities