89324-44-7

Basic information

• Product Name: 5-Formyl-3-thiophenecarboxylic acid
• Synonyms: 5-Formyl-3-thiophenecarboxylic acid
• CAS NO: 89324-44-7
• Molecular Formula: C₆H₄O₃S
• Molecular Weight: 156.16
• Mol File: 89324-44-7.mol
• Article Data: 4

Chemical Properties

• Melting Point: 185-187 °C(Solv: water (7732-18-5))
• Boiling Point: 371.4±27.0 °C(Predicted)
• Appearance: /
• Density: 1.514±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 3.60±0.10(Predicted)
• CAS DataBase Reference: 5-Formyl-3-thiophenecarboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 5-Formyl-3-thiophenecarboxylic acid(89324-44-7)
• EPA Substance Registry System: 5-Formyl-3-thiophenecarboxylic acid(89324-44-7)

Safety Data

• Hazardous Substances Data: 89324-44-7(Hazardous Substances Data)

Usage

Description

5-Formyl-3-thiophenecarboxylic acid is a chemical compound with the molecular formula C7H4O3S. It is a carboxylic acid derivative featuring a formyl group (CHO) and a thiophene ring, which is a five-membered aromatic ring that contains a sulfur atom. 5-Formyl-3-thiophenecarboxylic acid is recognized for its reactivity due to the formyl group and its potential biological activities, making it a significant player in organic synthesis and pharmaceutical research.

Uses

Used in Pharmaceutical Research and Organic Synthesis:
5-Formyl-3-thiophenecarboxylic acid serves as a crucial building block in the synthesis of various pharmaceutical compounds. Its unique structure and reactivity contribute to the development of new drugs and organic compounds.
Used in Anti-inflammatory and Anti-cancer Research:
5-Formyl-3-thiophenecarboxylic acid is utilized in research for its potential anti-inflammatory and anti-cancer properties. Its biological activities are of interest for the development of therapeutic agents targeting inflammation and cancer.
Used as an Intermediate in Chemical Production:
In the chemical industry, 5-Formyl-3-thiophenecarboxylic acid is employed as an intermediate in the production of other organic compounds. Its role in the synthesis of a wide range of chemicals underscores its value in chemical research and manufacturing processes.

Upstream product

• 58267-85-9 2-(4-bromo-thiophen-2-yl)-[1,3]dioxolane 
• 88-13-1 3-Thiophene carboxylic acid 
• 100523-84-0 2-bromothiophene-4-carboxylic acid 
• 109-72-8 n-butyllithium 
• 124-38-9 carbon dioxide 

Downstream Products

• 748772-94-3 [2-(2-amino-phenylamino)-ethyl]-[4-(piperidine-1-carbonyl)-thiophen-2-yl-methyl]-carbamic acid tert-butyl ester 
• 748772-98-7 [2-(2-isopropylamino-phenylamino)-ethyl]-[4-(piperidine-1-carbonyl)-thiophen-2-yl-methyl]-carbamic acid tert-butyl ester 
• 67808-67-7 5-formyl-3-thiophenecarboxylic acid ethyl ester 
• 67808-66-6 3-methoxycarbonyl-thiophene-5-carboxaldehyde 
• 1196060-27-1 5-(((5S,9R)-9-(4-([14C]-cyano)phenyl)-3-(3,5-dichlorophenyl)-1-methyl-2,4-dioxo-1,3,7-triazaspiro[4.4]nonan-7-yl)methyl)-thiophene-3-carboxylic acid 

Relevant articles and documents

CONDENSED HETEROCYCLIC COMPOUNDS AS CALCITONIN AGONISTS

The present invention relates to novel fused heterocyclic ring system compounds and methods for their use in the treatment and prevention of diseases or conditions which are related to irregular calcification.

Phosphorylamides, their preparation and use

A phosphorylamide derivative represented by the general formula (I): STR1 wherein R represents an amino group that may be substituted, or a salt thereof, possesses potent antibacterial activity against Helicobacter bacterium, especially Helicobacter pylori, and is useful for prevention or treatment of digestive diseases caused by Helicobacter bacterium, solely or in combination with an antacid or an acid secretion inhibitor.