5-(1H-Pyrrol-1-yl)-2-mercaptobenzimidazole

CAS Number: 172152-53-3

Molecular Formula: C11H9N3S

Purity: 5-(1H-Pyrrol-1-yl)-2-mercaptobenzimidazole 95% purity

About 5-(1H-Pyrrol-1-yl)-2-mercaptobenzimidazole

5-(1H-Pyrrol-1-yl)-2-mercaptobenzimidazole (CAS 172152-53-3) is a pivotal building block in the API intermediates market, primarily utilized for the sophisticated synthesis of Proton Pump Inhibitors such as Ilaprazole to ensure high-performance gastric acid inhibition. 5-(1H-pyrrol-1-yl)-1H-benzo[d]imidazole-2-thiol fu...

5-(1H-Pyrrol-1-yl)-2-mercaptobenzimidazole Specifications

CAS Number

172152-53-3

Molecular Formula

C11H9N3S

Molecular Weight

215.27 g/mol

IUPAC Name

5-(1H-pyrrol-1-yl)-1,3-dihydro-2H-benzimidazole-2-thione

Canonical SMILES

C1=CN(C=C1)C2C=CC3=NC(=S)NC3=C2

InChI Key

YYXGYVYKGRUILQ-UHFFFAOYSA-N

PubChem CID

21460501

MDL Number

MFCD15144909

HSN No

29339900

CAS Number

172152-53-3

Molecular Formula

C11H9N3S

Molecular Weight

215.27 g/mol

IUPAC Name

5-(1H-pyrrol-1-yl)-1,3-dihydro-2H-benzimidazole-2-thione

Canonical SMILES

C1=CN(C=C1)C2C=CC3=NC(=S)NC3=C2

InChI Key

YYXGYVYKGRUILQ-UHFFFAOYSA-N

PubChem CID

21460501

MDL Number

MFCD15144909

HSN No

29339900

Molecular Weight

215.27 g/mol

Purity

5-(1H-Pyrrol-1-yl)-2-mercaptobenzimidazole 95% purity

Physical appearance

White or light yellow crystalline powder

Boiling Point

381.7±44.0 °C (Predicted)

Freezing point

273°C

Flash Point

121.2 °C

Density

1.4 g/cm3

Precautionary Statement Codes

P261, P280, and P305+P351+P338

Hazard Classes and Categories

Acute Tox. 4 (100%) Skin Irrit. 2 (100%)

Pharmaceutical Intermediate

A key organic building block primarily utilized in the chemical synthesis of Ilaprazole, a proton pump inhibitor (PPI) used as an anti-ulcer medication for treating gastric and duodenal ulcers

Organic Synthesis Building Block

A functionalized benzimidazole derivative used in medicinal chemistry and drug discovery research for the development of novel bioactive molecules with antimicrobial, anti-inflammatory, and gastroprotective properties

Scientific Research Reagent

A specialized chemical reagent employed in academic and industrial laboratory settings for CRO chemical synthesis projects and the exploration of new avenues in heterocyclic chemistry.