2207-63-8

Basic information

• Product Name: 1-Propanone, 3-(2-furanyl)-1-phenyl-
• CAS NO: 2207-63-8
• Molecular Formula: C13H12O2
• Molecular Weight: 200.237
• Mol File: 2207-63-8.mol
• Article Data: 53

Chemical Properties

• CAS DataBase Reference: 1-Propanone, 3-(2-furanyl)-1-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Propanone, 3-(2-furanyl)-1-phenyl-(2207-63-8)
• EPA Substance Registry System: 1-Propanone, 3-(2-furanyl)-1-phenyl-(2207-63-8)

Safety Data

• Hazardous Substances Data: 2207-63-8(Hazardous Substances Data)

Usage

Type of compound

Ketone

Structural features

Furan ring and phenyl group

Usage

Synthesis of organic compounds and pharmaceuticals, building block for drug development, flavoring agent in food industry, development of advanced materials, reagent in organic chemistry reactions

Aromatic properties

Has a sweet, caramel-like aroma

Potential applications

Medicinal chemistry, flavoring agent, advanced materials development, organic chemistry reactions.

Upstream product

• 39511-12-1 (E)-3-(furan-2-yl)-1-phenyl-2-propen-1-one 
• 98-01-1 furfural 
• 98-86-2 acetophenone 
• 98-00-0 (2-furyl)methyl alcohol 
• 98-85-1 1-Phenylethanol 
• 536-74-3 phenylacetylene 
• 120134-60-3 (E)-3-(furan-2-yl)-1-phenylprop-2-en-1-ol 
• 4249-72-3 2-phenoxy-1-phenylethanol 
• 13331-23-2 fur-2-ylboronic acid 
• 936-59-4 3-chloropropiophenone 
• 717-21-5 3-(furan-1-yl)-1-phenyl-prop-2-en-1-one 
• 6118-51-0 exo-3,6-epoxy-1,2,3,6-tetrahydrophthalic anhydride 
• 64-17-5 ethanol 
• 67-56-1 methanol 

Downstream Products

• 5073-13-2 2-(3-phenylpropyl)furan 
• 93-89-0 benzoic acid ethyl ester 
• 1400793-00-1 1,1,1-trifluoro-4-(furan-2-yl)butan-2-one 
• 1436413-31-8 3-(furan-2-ylmethyl)-2-phenylquinoline 
• 5120-10-5 (+/-)(1Ξ,2Ξ)-1-(3-phenyl-propyl)-7-oxa-norborn-5-ene-2r,3c-dicarboxylic acid-anhydride 

Relevant articles and documents

Borane-Catalyzed, Chemoselective Reduction and Hydrofunctionalization of Enones Enabled by B-O Transborylation

The use of stoichiometric organoborane reductants in organic synthesis is well established. Here these reagents have been rendered catalytic through an isodesmic B-O/B-H transborylation applied in the borane-catalyzed, chemoselective alkene reduction and formal hydrofunctionalization of enones. The reaction was found to proceed by a 1,4-hydroboration of the enone and B-O/B-H transborylation with HBpin, enabling catalyst turnover. Single-turnover and isotopic labeling experiments supported the proposed mechanism of catalysis with 1,4-hydroboration and B-O/B-H transborylation as key steps.

Alkylation synthesis method of in-situ catalytic alcohol (by machine translation)

The method comprises VIB metal complexes, an auxiliary ligand and a base as a catalytic reaction system, wherein the alcohol serves as an alkylating agent, and the nucleophilic substrate is subjected to in-situ catalytic alkylation reaction in a solvent and an inert gas atmosphere. The catalytic system has a wide application range on a substrate, can catalyze the synthesis of C-N and C-C bond compounds of different structures under mild conditions, and can green synthesize a series of valuable N - alkylation and C - alkylation compounds. (by machine translation)

Chemoselective Hydrosilylation of the α,β-Site Double Bond in α,β- And α,β,γ,δ-Unsaturated Ketones Catalyzed by Macrosteric Borane Promoted by Hexafluoro-2-propanol

The B(C6F5)3-catalyzed chemoselective hydrosilylation of α,β- and α,β,γ,δ-unsaturated ketones into the corresponding non-symmetric ketones in mild reaction conditions is developed. Nearly 55 substrates including those bearing reducible functional groups such as alkynyl, alkenyl, cyano, and aromatic heterocycles are chemoselectively hydrosilylated in good to excellent yields. Isotope-labeling studies revealed that hexafluoro-2-propanol also served as a hydrogen source in the process.