22927-31-7

Basic information

• Product Name: Butanal, 4-(benzoyloxy)-
• CAS NO: 22927-31-7
• Molecular Formula: C11H12O3
• Molecular Weight: 192.214
• Mol File: 22927-31-7.mol
• Article Data: 14

Chemical Properties

• CAS DataBase Reference: Butanal, 4-(benzoyloxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Butanal, 4-(benzoyloxy)-(22927-31-7)
• EPA Substance Registry System: Butanal, 4-(benzoyloxy)-(22927-31-7)

Safety Data

• Hazardous Substances Data: 22927-31-7(Hazardous Substances Data)

Upstream product

• 201230-82-2 carbon monoxide 
• 583-04-0 vinyl benzoate 
• 29264-40-2 5-pentenylbenzoate 
• 32651-37-9 4-benzoyloxybutan-1-ol 
• 2749-68-0 2-phenyl-[1,3]dioxepane 
• 122471-85-6 3-butynyl benzoate 
• 98-88-4 benzoyl chloride 
• 18203-32-2 3-butenyl benzoate 
• 65-85-0 benzoic acid 

Downstream Products

• 84629-13-0 8-(Benzoyloxy)-2,5-octandion 
• 605671-58-7 2-[3'-(benzoyloxy)propyl]-1,3-dithiolane 
• 1203584-31-9 ethyl (E)-6-(benzoyloxy)-2-methylhex-2-enoate 
• 1193376-74-7 C₄₃H₅₄O₇SSi 
• 1192815-37-4 C₃₄H₄₃ClO₄Si 
• 1192815-38-5 C₃₄H₄₃ClO₄Si 
• 1238759-86-8 methyl 2-(3-(benzoyloxy)propyl)-2,5-dihydrooxazole-4-carboxylate 
• 1253282-54-0 C₁₈H₁₉NO₃ 
• 1253282-53-9 C₁₈H₁₉NO₃ 
• 100-42-5 styrene 
• 1442649-93-5 (R)-4-(naphthalen-2-yl)pentyl benzoate 
• 1442649-52-6 (S)-4-(2-(methylthio)acetoxy)-4-(naphthalen-2-yl)butylbenzoate 
• 1430475-45-8 (S)-4-hydroxy-4-(naphthalen-2-yl)butyl benzoate 
• 854759-73-2 benzoic acid 6-(1-methyl-2,5-dioxo-cyclopentyl)-4-oxo-hexyl ester 

Relevant articles and documents

Micellar Catalysis for Sustainable Hydroformylation

It is here reported a fully sustainable and generally applicable protocol for the regioselective hydroformylation of terminal alkenes, using cheap commercially available catalysts and ligands, in mild reaction conditions (70 °C, 9 bar, 40 min). The process can take advantages from both micellar catalysis and microwave irradiation to obtain the linear aldehydes as the major or sole regioisomers in good to high yields. The substrate scope is largely explored as well as the application of hydroformylation in tandem with intramolecular hemiacetalization thus demonstrating the compatibility with a broad variety of functional groups. The reaction is efficient even in large scale and the catalyst and micellar water phase can be reused at least 5 times without any impact in reaction yields. The efficiency and sustainability of this protocol is strictly related to the in situ transformation of the aldehyde into the corresponding Bertagnini's salt that precipitates in the reaction mixture avoiding organic solvent mediated purification steps to obtain the final aldehydes as pure compounds.

Design, synthesis, and in vitro evaluation of 4-aminoalkyl-1(2H)-phthalazinones as potential multifunctional anti-Alzheimer's disease agents

A series of 4-aminoalkyl-1(2H)-phthalazinone derivatives was designed and synthesized as potential multifunctional agents for Alzheimer's disease (AD) treatment. In vitro biological assay results demonstrated that most synthesized compounds exhibited sign

Axial-to-Central Chirality Transfer for Construction of Quaternary Stereocenters via Dearomatization of BINOLs

All-carbon quaternary stereocenters are versatile building blocks, and their asymmetric construction has attracted much attention. Herein, we disclose an axial-to-central chirality transfer strategy for the synthesis of chiral quaternary stereocenters via dearomatization of (S)-BINOLs. The reaction proceeded smoothly with a wide range of propargyl carbonates to afford chiral spiro-compounds in high yields with excellent enantioselectivities. In addition, the strategy was extended to kinetic resolution of rac-BINOLs albeit with moderate s value.