32358-94-4

Basic information

• Product Name: 5-(5-Methylthiophen-2-yl)thiophene-2-carbaldehyde
• Synonyms: 5-(5-Methylthiophen-2-yl)thiophene-2-carbaldehyde;5-(5-Methylthiophen-2-yl)thiophene-2-carbaldehyde 97%;5'-methyl-[2,2'-bithiophene]-5-carbaldehyde
• CAS NO: 32358-94-4
• Molecular Formula: C₁₀H₈OS₂
• Molecular Weight: 208.29992
• Mol File: 32358-94-4.mol
• Article Data: 6

Chemical Properties

• Melting Point: 96-100°C
• Appearance: /
• CAS DataBase Reference: 5-(5-Methylthiophen-2-yl)thiophene-2-carbaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(5-Methylthiophen-2-yl)thiophene-2-carbaldehyde(32358-94-4)
• EPA Substance Registry System: 5-(5-Methylthiophen-2-yl)thiophene-2-carbaldehyde(32358-94-4)

Safety Data

• Hazard Codes: Xn
• Statements: 22-38
• WGK Germany: 3
• Hazardous Substances Data: 32358-94-4(Hazardous Substances Data)

Upstream product

• 18494-74-1 2-methyl-2,5'-bithiophene 
• 554-14-3 2-Methylthiophene 
• 5370-19-4 5-iodothiophene-2-carbaldehyde 
• 135887-14-8 5-hydroxymethyl-5'-methyl-2,2'-bithienyl 
• 68-12-2 N,N-dimethyl-formamide 
• 146796-00-1 5'-bromo-5-methyl-2,2'-bithiophene 
• 4701-17-1 5-bromo-2-thiophencarboxaldehyde 
• 162607-20-7 (5-methylthiophen-2-yl)boronic acid 
• 765-58-2 2-bromo-5-methyl thiophene 
• 98-03-3 thiophene-2-carbaldehyde 
• 636-72-6 2-thiophenemethanol 
• 13781-27-6 2-Hydroxymethyl-5-iodothiophene 
• 3779-27-9 2,2'-bithiophene-5-carboxaldehyde 
• 492-97-7 2,2'-Bithiophene 

Downstream Products

• 101607-27-6 2-(4-chloro-phenyl)-3c-(5'-methyl-[2,2']bithienyl-5-yl)-acrylonitrile 
• 16303-58-5 5,5'-dimethyl-2,2'-dithiophene 

Relevant articles and documents

Design and Syntheses of Palladium Complexes of NNN/CNN Pincer Ligands: Catalyst for Cross Dehydrogenative Coupling Reaction of Heteroarenes

This report describes simple syntheses of a new class of palladium(II) pincer complexes having NNN and CNN coordination modes. The new complexes were fully characterized with the help of 1H and 13C{1H} NMR, HRMS, and IR sp

Controlling stereochemical outcomes of asymmetric processes by catalyst remote molecular functionalizations: Chiral diamino-oligothiophenes (DATs) as ligands in asymmetric catalysis

The synthesis, characterization, and structure-guided application of a new class of highly versatile chiral C2-symmetric diamine-oligothiophene ligands in Pd-catalyzed asymmetric transformations are presented. Experimental investigations of the

Photochemical reactions of Thienyl-, Bithienyl-, Terthienyl- and Thienylaroyl-methanols

Photochemical reactions of some thienyl-, bithienyl-, terthienyl- and thienylaroyl-methanols were studied in the neat state as well as in solvents like methanol and benzene.The terthienylmethanols were found to be susceptible to photo-sensitized oxidation which was inhibited by singlet oxygen quenchers.The photoproducts were isolated, characterised by spectroscopic methods and in some cases by synthesis.