58751-63-6

Basic information

• Product Name: 3-(2-nitrobenzene)-1-phenylpropan-1-one
• Synonyms: 3-(2-nitrobenzene)-1-phenylpropan-1-one
• CAS NO: 58751-63-6
• Molecular Weight: 255.273
• Mol File: 58751-63-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 3-(2-nitrobenzene)-1-phenylpropan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(2-nitrobenzene)-1-phenylpropan-1-one(58751-63-6)
• EPA Substance Registry System: 3-(2-nitrobenzene)-1-phenylpropan-1-one(58751-63-6)

Safety Data

• Hazardous Substances Data: 58751-63-6(Hazardous Substances Data)

Upstream product

• 98-86-2 acetophenone 
• 552-89-6 2-nitro-benzaldehyde 
• 1466-88-2 2-nitrocinnamic aldehyde 
• 98-80-6 phenylboronic acid 
• 53744-31-3 2-nitrochalcone 
• 13735-81-4 1-styrenyloxytrimethylsilane 
• 3958-60-9 2-nitrophenylmethyl bromide 
• 4393-06-0 1-Phenyl-2-propen-1-ol 
• 577-19-5 2-nitrophenyl bromide 
• 71-43-2 benzene 
• 1083-30-3 dihydrochalcone 

Downstream Products

• 3377-72-8 2-benzylindole 
• 612-96-4 2-Phenylquinoline 
• 108716-29-6 3-(2-nitro-phenyl)-1-phenyl-propan-1-ol 
• 24005-23-0 2-phenyl-1,2,3,4-tetrahydroquinoline 

Relevant articles and documents

The Heck reaction of allylic alcohols catalysed by an N-heterocyclic carbene-Pd(ii) complex and toxicity of the ligand precursor for the marine benthic copepod: Amphiascoides atopus

The palladium-catalysed reaction of aryl halides and allylic alcohols is an attractive method for obtaining α,β-unsaturated aldehydes and ketones, which represent key intermediates in organic synthesis. In this context, a 1,2,3-triazol-5-ylidene (aNHC)-based palladium(ii) complex formed in situ has been found to be a selective catalyst for the syntheses of building blocks from the corresponding aryl halides and allylic alcohols, with yields ranging from 50% to 90%. The lack of toxic effects of the ligand precursor (1,2,3-triazolium salt) of the palladium(ii) complex for the harpacticoid copepod Amphiascoides atopus allowed us to contrast the efficiency of the catalytic system with the potential impact of the principal waste chemical in global aquatic ecosystems, which has not been previously addressed.

Dirhodium(ii)/P(t-Bu)3 catalyzed tandem reaction of α,β-unsaturated aldehydes with arylboronic acids

Phosphine ligated dirhodium(ii) acetate is advocated as a catalyst for the synthesis of aryl alkyl ketones by the tandem reaction of α,β-unsaturated aromatic or aliphatic aldehydes with arylboronic acids. This tandem procedure included arylation followed by the isomerization reaction. This method exhibits good functional group tolerance and has a broad substrate scope. With the conjugated aldehydes, the one-step synthesis of γ,δ-unsaturated ketones was realized through this reaction. It is noteworthy that the length of the Rh-P bond is an important factor affecting catalytic reactions. The comparative analysis of the crystal structures of axially alkylphosphane and arylphosphane ligated dirhodium(ii) acetate revealed that the shorter Rh-P bond length favors the isomerization process as compared to the longer one. In addition, the dirhodium(ii) compound can be recovered after the completion of the reaction.

Visible-light-induced intermolecular atom-transfer radical addition of benzyl halides to olefins: Facile synthesis of tetrahydroquinolines

Cu(dap)2Cl has been utilized as a visible-light photoredox catalyst for the atom-transfer radical addition (ATRA) of benzyl halides to styrenes and silyl enol ethers. The resulting ATRA products can be readily converted into tetrahydroquinoline