33342-29-9

Basic information

• Product Name: 2-Furanmethanol, 5-(4-chlorophenyl)-
• Synonyms: 2-Furanmethanol, 5-(4-chlorophenyl)-
• CAS NO: 33342-29-9
• Molecular Formula: C₁₁H₉ClO₂
• Molecular Weight: 208.65
• Mol File: 33342-29-9.mol
• Article Data: 8

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Furanmethanol, 5-(4-chlorophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Furanmethanol, 5-(4-chlorophenyl)-(33342-29-9)
• EPA Substance Registry System: 2-Furanmethanol, 5-(4-chlorophenyl)-(33342-29-9)

Safety Data

• Hazardous Substances Data: 33342-29-9(Hazardous Substances Data)

Upstream product

• 57753-80-7 5-(4-chloro-phenyl)-furan-2-carbonyl chloride 
• 88-14-2 2-furanoic acid 
• 41019-45-8 5-(4-chlorophenyl)-2-furoic acid 
• 1584709-72-7 (S)-3-(benzyloxy)-1-(4-chlorophenyl)-3-((S)-2,2-dimethyl-1,3-dioxolan-4-yl)propan-1-one 
• 106-47-8 4-chloro-aniline 
• 98-01-1 furfural 
• 1679-18-1 4-Chlorophenylboronic acid 
• 344943-62-0 4-methylbenzenesulfonyl N'-(5-(4-bromophenyl)furan-2-ylmethylene)hydrazide 
• 34035-03-5 5-(4-chlorophenyl)-2-furaldehyde 

Downstream Products

• 1032338-25-2 C₁₉H₁₂Cl₃NO₄ 
• 1032338-02-5 C₁₉H₁₂ClF₂NO₄ 
• 62645-46-9 Bis-<5-(4-Chlorphenyl)-2-furyl>-methan 
• 17221-37-3 2-(4-chlorophenyl)furan 
• 62806-34-2 (E)-3-[5-(4-chlorophenyl)-2-furyl]-2-propenoic acid 

Relevant articles and documents

Synthesis and bioactivity of phenyl substituted furan and oxazole carboxylic acid derivatives as potential PDE4 inhibitors

In this present study, a series of 5-phenyl-2-furan and 4-phenyl-2-oxazole derivatives were designed and synthesized as phosphodiesterase type 4 (PDE4) inhibitors. In vitro results showed that the synthesized compounds exhibited considerable inhibitory ac

PROCESS FOR THE SYNTHESIS OF ARYLDIAZONIUM SALTS USING NITROGEN OXIDES IN OXYGEN-CONTAINING GAS STREAMS, ESPECIALLY FROM INDUSTRIAL WASTE GASES

The present invention relates to a process for the synthesis of aryldiazonium salts using nitrogen oxides in oxygen-containing gas streams, especially from industrial waste gases.

2-amino-3-(5-phenylfuran-2-yl)propionic acids and 5-phenylfuran-2-ylacrylic acids are novel substrates of phenylalanine ammonia-lyase

Both racemic 2-amino-3-(5-phenylfuran-2-yl)propionic acids and 5-phenylfuran-2-ylacrylic acids were synthesized and spectroscopically characterized (UV, EI-MS, 1H-NMR and 13C-NMR). The phenyl group of the 5-phenylfuranyl residue carried no (rac-la) para-Br (rac-lb) or Cl para or ortho (rac-lc, d) substituents. The novel furanylalanines were used as substrates of recombinant phenylalanine ammonia-lyase (PAL). When 50% of the racemic 5-phenylfuranylalanines were converted into the corresponding acrylates, the D-enantiomers of the substrates could be isolated. The L-enantiomers could be prepared from the substituted acrylates when the PAL reaction was reversed in the presence of 6 M ammonia at pH 10. The Japan Institute of Heterocyclic Chemistry.