215320-36-8

Basic information

• Product Name: 4-(3-FLUOROPHENYL)-1-BUTEN-4-OL
• Synonyms: 4-(3-FLUOROPHENYL)-1-BUTEN-4-OL
• CAS NO: 215320-36-8
• Molecular Formula: C₁₀H₁₁FO
• Molecular Weight: 166.19
• Mol File: 215320-36-8.mol
• Article Data: 12

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-(3-FLUOROPHENYL)-1-BUTEN-4-OL(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(3-FLUOROPHENYL)-1-BUTEN-4-OL(215320-36-8)
• EPA Substance Registry System: 4-(3-FLUOROPHENYL)-1-BUTEN-4-OL(215320-36-8)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 215320-36-8(Hazardous Substances Data)

Upstream product

• 107-05-1 3-chloroprop-1-ene 
• 456-48-4 3-Fluorobenzaldehyde 
• 1730-25-2 allylmagnesium bromide 
• 24850-33-7 allyltributylstanane 
• 106-95-6 allyl bromide 
• 2622-05-1 allylmagnesium bromide 
• 107-18-6 allyl alcohol 
• 556-56-9 allyl iodid 

Downstream Products

• 865776-79-0 1-fluoro-3-(1-methoxy-but-3-enyl)-benzene 
• 1027966-05-7 C₁₅H₂₁FOSi 
• 1616603-14-5 2-(3-fluorophenyl)-1H-pyrrole 
• 1616603-23-6 C₁₂H₁₂FNO₂ 
• 904672-48-6 1-(3-fluorophenyl)but-3-en-1-one oxime 
• 939024-94-9 C₁₆H₂₀F₄O₂Si 
• 1027300-26-0 C₁₄H₂₁FOSi 
• 1027172-29-7 C₁₃H₁₇FOSi 
• 904672-61-3 1-(3-fluoro-phenyl)-but-3-en-1-one 
• 406486-91-7 4β-acetoxy-2β,6β-diethyl-tetrahydropyran 
• 456-48-4 3-Fluorobenzaldehyde 
• 865776-93-8 2-amino-5-[2-(3-fluoro-phenyl)-2-methoxy-ethyl]-thiazole-4-carboxylic acid methyl ester 
• 865777-11-3 5-[2-(3-fluoro-phenyl)-2-methoxy-ethyl]-thiazole-4-carboxylic acid 
• 865777-02-2 5-[2-(3-fluoro-phenyl)-2-methoxy-ethyl]-thiazole-4-carboxylic acid methyl ester 

Relevant articles and documents

Visible Light-Promoted Recyclable Carbon Nitride-Catalyzed Dioxygenation of β,γ-Unsaturated Oximes

A visible-light-induced dioxygenation of β,γ-unsaturated oximes for the synthesis of diverse useful isoxazolines bearing a hydroxyl moiety was developed by employing graphitic carbon nitride (g-C3N4) as a heterogeneous photocatalyst under an air atmosphere. Noted that, the eminent advantages of this metal-free protocol include step economy, easy operation, a recyclable photocatalyst, external reductant-/oxidant-free and mild reaction conditions. Additionally, mechanistic studies indicated hydroxyl radical was generated under the photocatalysis of g-C3N4.

Copper-Promoted 6- endo-trig Cyclization of β,γ-Unsaturated Hydrazones for the Synthesis of 1,6-Dihydropyridazines

A novel and efficient strategy for the synthesis of 1,6-dihydropyridazines via copper-promoted 6-endo-trig cyclization of readily available β,γ-unsaturated hydrazones have been developed. A series of 1,6-dihydropyridazines have been synthesized by this method with good yields, high functional group tolerance, and remarkable regioselectivity under mild conditions. Importantly, the 1,6-dihydropyridazines can be efficiently converted to biologically important pyridazines in the presence of NaOH.

Copper-catalyzed 5-endo-trig cyclization of ketoxime carboxylates: A facile synthesis of 2-arylpyrroles

A novel and facile copper-catalyzed 5-endo-trig cyclization of ketoxime carboxylates for the synthesis of 2-arylpyrroles has been developed. The reaction tolerates a range of functional groups and is a practical procedure for rapid synthesis of 2-arylpyrroles in high yields under mild conditions. the Partner Organisations 2014.