83822-33-7

Basic information

• Product Name: 2-AMINO-4,5,6,7-TETRAHYDRO-BENZO[B]THIOPHENE-3-CARBOXYLIC ACID (4-METHOXY-PHENYL)-AMIDE
• Synonyms: ART-CHEM-BB B014525;2-AMINO-4,5,6,7-TETRAHYDRO-BENZO[B]THIOPHENE-3-CARBOXYLIC ACID (4-METHOXY-PHENYL)-AMIDE;TIMTEC-BB SBB001243;2-amino-N-(4-methoxyphenyl)-4,5,6,7-tetrahydrobenzothiophene-3-carboxamide
• CAS NO: 83822-33-7
• Molecular Formula: C₁₆H₁₈N₂O₂S
• Molecular Weight: 302.39
• Product Categories: Thiophene
• Mol File: 83822-33-7.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 466.6 °C at 760 mmHg
• Flash Point: 236 °C
• Appearance: /
• Density: 1.309 g/cm³
• Vapor Pressure: 6.98E-09mmHg at 25°C
• Refractive Index: 1.676
• CAS DataBase Reference: 2-AMINO-4,5,6,7-TETRAHYDRO-BENZO[B]THIOPHENE-3-CARBOXYLIC ACID (4-METHOXY-PHENYL)-AMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-AMINO-4,5,6,7-TETRAHYDRO-BENZO[B]THIOPHENE-3-CARBOXYLIC ACID (4-METHOXY-PHENYL)-AMIDE(83822-33-7)
• EPA Substance Registry System: 2-AMINO-4,5,6,7-TETRAHYDRO-BENZO[B]THIOPHENE-3-CARBOXYLIC ACID (4-METHOXY-PHENYL)-AMIDE(83822-33-7)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 83822-33-7(Hazardous Substances Data)

Usage

Description

2-AMINO-4,5,6,7-TETRAHYDRO-BENZO[B]THIOPHENE-3-CARBOXYLIC ACID (4-METHOXY-PHENYL)-AMIDE is a chemical compound derived from benzo[b]thiophene, featuring a heterocyclic ring structure with a sulfur atom. The incorporation of an amino group and a carboxylic acid group enhances its functionality, allowing for potential interactions with biological systems. The presence of a 4-methoxy-phenyl group adds chemical diversity and may influence the compound's biological activity, making it a promising candidate for pharmaceutical and research applications.

Uses

Used in Pharmaceutical Industry:
2-AMINO-4,5,6,7-TETRAHYDRO-BENZO[B]THIOPHENE-3-CARBOXYLIC ACID (4-METHOXY-PHENYL)-AMIDE is used as a pharmaceutical candidate for its potential medicinal properties. 2-AMINO-4,5,6,7-TETRAHYDRO-BENZO[B]THIOPHENE-3-CARBOXYLIC ACID (4-METHOXY-PHENYL)-AMIDE's unique structure and functional groups enable it to interact with biological systems, making it a valuable tool for drug discovery and development efforts.
Used in Research Applications:
In the field of research, 2-AMINO-4,5,6,7-TETRAHYDRO-BENZO[B]THIOPHENE-3-CARBOXYLIC ACID (4-METHOXY-PHENYL)-AMIDE serves as a valuable chemical entity for exploring its potential interactions with biological systems. Its diverse chemical structure allows researchers to investigate its properties and applications in various scientific studies, contributing to the advancement of knowledge in the field.

InChI:InChI=1/C16H18N2O2S/c1-20-11-8-6-10(7-9-11)18-16(19)14-12-4-2-3-5-13(12)21-15(14)17/h6-9H,2-5,17H2,1H3,(H,18,19)

Upstream product

• 5382-38-7 2-cyano-N-(4-methoxyphenyl)acetamide 
• 108-94-1 cyclohexanone 
• 104-94-9 4-methoxy-aniline 
• 89733-18-6 2-Cyano-2-cyclohexylidene-N-(4-methoxy-phenyl)-acetamide 

Downstream Products

• 83822-27-9 3-(4-Methoxy-phenyl)-5,6,7,8-tetrahydro-3H-benzo[4,5]thieno[2,3-d]pyrimidin-4-one 
• 85919-09-1 N-[3-(4-Methoxy-phenylcarbamoyl)-4,5,6,7-tetrahydro-benzo[b]thiophen-2-yl]-oxalamic acid ethyl ester 

Relevant articles and documents

Barium aluminate nano-powders efficient catalyst for the synthesis of novel benzo[b]thiophene, thieno[2,3-c]thiopyran and thieno[2,3-c]pyridine derivatives

Uniform nanopowders of barium aluminate (BaAl2O4) can be synthesized by a facile solution reaction at room temperature using barium and aluminum salts and 2-aminoethanol as a precipitating agent. The asprepared sample showed a good reactivity in the synthesis of benzo[b]thiophene, thieno[2,3-c]thiopyran and thieno[2,3-c]pyridine derivatives. Comparatively the method is efficient and eco-friendly, and finally, a range of compounds with variable functionalities in excellent yield can be achieved.

On thieno compounds. Part IV: 3-aryl-3,4-dihydro-4-oxobenzo[b]thieno[2,3-d]pyrimidines

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