216443-17-3

Basic information

• Product Name: 3'-METHYL [1,1'-BIPHENYL]-2-CARBOXALDEHYDE
• Synonyms: 3'-METHYL[1,1'-BIPHENYL]-2-CARBALDEHYDE;3'-METHYL [1,1'-BIPHENYL]-2-CARBOXALDEHYDE;3'-METHYL-BIPHENYL-2-CARBALDEHYDE;3'-METHYL-BIPHENYL-2-CARBOXALDEHYDE;AKOS BAR-0185;2-(3-Methylphenyl)benzaldehyde
• CAS NO: 216443-17-3
• Molecular Formula: C₁₄H₁₂O
• Molecular Weight: 196.24
• Mol File: 216443-17-3.mol
• Article Data: 22

Chemical Properties

• Boiling Point: 338.2 °C at 760 mmHg
• Flash Point: 184.7 °C
• Appearance: /
• Density: 1.074 g/cm³
• CAS DataBase Reference: 3'-METHYL [1,1'-BIPHENYL]-2-CARBOXALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 3'-METHYL [1,1'-BIPHENYL]-2-CARBOXALDEHYDE(216443-17-3)
• EPA Substance Registry System: 3'-METHYL [1,1'-BIPHENYL]-2-CARBOXALDEHYDE(216443-17-3)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 216443-17-3(Hazardous Substances Data)

Usage

General Description

3'-Methyl [1,1'-biphenyl]-2-carboxaldehyde is a chemical compound with the molecular formula C14H12O. It is a derivative of biphenyl, an aromatic hydrocarbon. This chemical has a benzaldehyde group, which is a common building block in organic synthesis. It has a strong odor and is used as a flavor and fragrance ingredient. Additionally, it has potential applications in medicinal chemistry and as a starting material for the synthesis of other organic compounds. However, it should be handled with caution as it may pose some health hazards if not used properly.

Upstream product

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• 89-98-5 2-chloro-benzaldehyde 

Downstream Products

• 1292302-47-6 3-methyl-9-[(4-methylphenyl)sulfonylamino]fluorene 
• 1304460-87-4 C₂₁H₁₉NO₂S 
• 1399841-58-7 C₂₀H₁₈O 
• 2523-39-9 3-methylfluorene 
• 1730-37-6 1-methylfluorene 

Relevant articles and documents

Electrochemical Decarboxylative Cyclization of α-Amino-Oxy Acids to Access Phenanthridine Derivatives

Phenanthridines are a class of useful heterocycles in the field of drug development. In this work, a method via electrochemical decarboxylative cyclization of α-amino-oxy acids to access phenanthridine derivatives was developed. This reaction proceeded th

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A facile gold-catalyzed oxidation terminal alkynes to synthesize substituted dihydronaphthalen-2(1H)-ones 3 and phenanthrenols 5 was realized. Various useful structures and drug precursors were generated in up to 99% yield under mild condition and low catalyst loading.