26170-87-6

Basic information

• Product Name: 4-PHENYL-2-THIOPHENECARBOXALDEHYDE 96
• Synonyms: 4-PHENYL-2-THIOPHENECARBOXALDEHYDE 96;4-Phenylthiophene-2-carboxaldehyde;4-Phenylthiophene-2-carboxaldehyde,4-Phenyl-2-thiophenecarboxaldehyde;4-Phenylthiophene-2-carboxaldehyde 96%
• CAS NO: 26170-87-6
• Molecular Formula: C₁₁H₈OS
• Molecular Weight: 188.24562
• Product Categories: Aldehydes;Building Blocks;C10 to C20+;C10-C12;Carbonyl Compounds;Chemical Synthesis;Heterocyclic Building Blocks;Organic Building Blocks;Thiophenes
• Mol File: 26170-87-6.mol
• Article Data: 15

Chemical Properties

• Melting Point: 67-71 °C(lit.)
• Boiling Point: 312.4 °C at 760 mmHg
• Flash Point: 118.1 °C
• Appearance: /
• Density: 1.207 g/cm³
• Vapor Pressure: 0.000531mmHg at 25°C
• Refractive Index: 1.637
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• CAS DataBase Reference: 4-PHENYL-2-THIOPHENECARBOXALDEHYDE 96(CAS DataBase Reference)
• NIST Chemistry Reference: 4-PHENYL-2-THIOPHENECARBOXALDEHYDE 96(26170-87-6)
• EPA Substance Registry System: 4-PHENYL-2-THIOPHENECARBOXALDEHYDE 96(26170-87-6)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 26170-87-6(Hazardous Substances Data)

Usage

General Description

4-PHENYL-2-THIOPHENECARBOXALDEHYDE 96 is a chemical compound that consists of a phenyl group attached to a thiophene ring with a carboxaldehyde functional group. It is commonly used as an intermediate in the synthesis of pharmaceuticals and other organic compounds. This chemical is known for its strong and distinctive odor. Additionally, it is often utilized in research and development of new materials and as a building block in the production of various aromatic compounds. Overall, 4-PHENYL-2-THIOPHENECARBOXALDEHYDE 96 plays a crucial role in the creation and transformation of numerous important chemical products.

InChI:InChI=1/C11H8OS/c12-7-11-6-10(8-13-11)9-4-2-1-3-5-9/h1-8H

Upstream product

• 5558-04-3 1-cyclopropyl-1-phenylethanol 
• 18791-75-8 4-Bromothiophen-2-aldehyde 
• 24388-23-6 2-phenyl-4,4,5,5-tetramethyl-1,3,2-dioxoborole 
• 2404-87-7 3-phenylthiophene 
• 68-12-2 N,N-dimethyl-formamide 
• 60231-03-0 2-phenyl-3-chloropropenal 
• 21676-90-4 methyl 4-phenylthiophene-2-carboxylate 
• 98-80-6 phenylboronic acid 
• 79757-76-9 4-phenyl-2-thiophenemethanol 
• 98-03-3 thiophene-2-carbaldehyde 
• 71-43-2 benzene 

Downstream Products

• 1029571-41-2 C₁₆H₁₃N₃OS 
• 1008771-86-5 4-[(4-phenyl-2-thienyl)methyl]-N-pyrazin-2-ylpiperazine-1-carboxamide 
• 941281-24-9 (E)-2-methyl-3-(4-phenylthiophen-2-yl)acrylic acid 
• 2404-87-7 3-phenylthiophene 

Relevant articles and documents

Metal-Free Aerobic Oxidative Selective C-C Bond Cleavage in Heteroaryl-Containing Primary and Secondary Alcohols

A transition-metal-free aerobic oxidative selective C-C bond-cleavage reaction in primary and secondary heteroaryl alcohols is reported. This reaction was highly efficient and tolerated various heteroaryl alcohols, generating a carboxylic acid derivative and a neutral heteroaromatic compound. Experimental studies combined with density functional theory calculations revealed the mechanism underlying the selective C-C bond cleavage. This strategy also provides an alternative simple approach to carboxylation reaction.

Furan- and thiophene-2-carbonyl amino acid derivatives activate hypoxia-inducible factor via inhibition of factor inhibiting hypoxia-inducible factor-1

Induction of a series of anti-hypoxic proteins protects cells during exposure to hypoxic conditions. Hypoxia-inducible factor-α (HIF-α) is a major transcription factor that orchestrates this protective effect. To activate HIF exogenously, without exposing

Substituted furopyridinediones as novel inhibitors of α-glucosidase

The global preponderance of diabetes mellitus has prompted the medical community to opt for various therapeutic solutions to curb this menace. One of the means involved controlling the post prandial hyperglycemia. α-Glucosidase inhibitors are known to be