174623-07-5

Usage

Uses

4-(5-Formyl-2-thienyl)benzoic Acid is a useful intermediate in organic synthesis.

Upstream product

• 98-03-3 thiophene-2-carbaldehyde 
• 150-13-0 4-amino-benzoic acid 
• 4701-17-1 5-bromo-2-thiophencarboxaldehyde 
• 99768-12-4 4-methoxycarbonylphenylboronic acid 
• 639816-37-8 4-(5-formyl-2-thiophenyl)benzoic acid methyl ester 

Downstream Products

• 618913-75-0 2-(4-carboxyphenyl)-5-(6-cyanobenzothiazol-2-yl)thiophene 
• 618913-79-4 2-(4-chlorocarbonylphenyl)-5-(6-cyanobenzothiazol-2-yl)thiophene 
• 1313398-23-0 4-(5-formylthiophen-2-yl)-N-methylbenzamide 
• 1313397-43-1 N-methyl-4-(5-((5-oxo-2-thioxoimidazolidin-4-ylidene)-methyl)thiophen-2-yl)benzamide 
• 1313398-24-1 4-(5-formylthiophen-2-yl)-N,N-dimethylbenzamide 
• 1313397-44-2 N,N-dimethyl-4-(5-((5-oxo-2-thioxoimidazolidin-4-ylidene)methyl)thiophen-2-yl)benzamide 
• 1313398-33-2 4-(5-formylthiophen-2-yl)-N-(2-morpholinoethyl)benzamide 
• 1313397-50-0 N-(2-morpholinoethyl)-4-(5-((5-oxo-2-thioxoimidazolidin-4-ylidene)methyl)thiophen-2-yl)benzamide 
• 1313398-29-6 4-(5-formylthiophen-2-yl)-N-(3-morpholinopropyl)benzamide 
• 1313397-48-6 N-(3-morpholinopropyl)-4-(5-((5-oxo-2-thioxoimidazolidin-4-ylidene)methyl)thiophen-2-yl)benzamide 
• 1313398-27-4 4-(5-formylthiophen-2-yl)-N-(2-hydroxyethyl)benzamide 
• 1313397-47-5 N-(2-hydroxyethyl)-4-(5-((5-oxo-2-thioxoimidazolidin-4-ylidene)methyl)thiophen-2-yl)benzamide 
• 1313398-31-0 4-(5-formylthiophen-2-yl)-N-(3-hydroxypropyl)benzamide 
• 1313397-49-7 N-(3-hydroxypropyl)-4-(5-((5-oxo-2-thioxoimidazolidin-4-ylidene)methyl)thiophen-2-yl)benzamide 

Relevant academic research and scientific papers

HETEROCYCLIC INTEGRIN AGONISTS

The present invention provides polycyclic oxothioxoimidazolidines, dioxoimidazolines, oxothioxooxazolidines, dioxooxazolidines, and related compounds, which are useful as integrin agonists. Methods for the treatment of integrin-mediated diseases such as cancer are also described.

Phospholipase D inhibitors and uses thereof

The invention is directed to thiazolidinones and the use thereof to inhibit phospholipase D (PLD) activity. The invention further relates to methods of treating cancer and inflammatory diseases using thiazolidinones.

Synthesis of new cyano-substituted bis-benzothiazolyl arylfurans and arylthiophenes

The new compounds 2-[4-(6-cyanobenzothiazol-2-yl)phenyl]-5-(6-cyano- benzothiazol-2-yl)furan (6a) and 2-[4-(6-Cyanobenzothiazol-2-yl)phenyl]-5-(6- cyano-benzothiazol-2-yl)thiophene (6b) were synthesized by multi-step reactions from the corresponding 2-fur

Synthesis and Fluorescent Properties of Some New Unsymmetric bis-Benzothiazolyl Furans and Thiophenes

Some new mono- and bis-benzothiazolyl compounds with furan and thiophene nuclei were synthesized by multistep reactions from the corresponding furan and thiophene aldehydes.The data obtained from emission spectra show a large influence of the benzothiazol