71787-53-6

Basic information

• Product Name: Benzonitrile, 4-(1-hydroxy-3-butenyl)-
• CAS NO: 71787-53-6
• Molecular Formula: C11H11NO
• Molecular Weight: 173.214
• Mol File: 71787-53-6.mol
• Article Data: 51

Chemical Properties

• CAS DataBase Reference: Benzonitrile, 4-(1-hydroxy-3-butenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzonitrile, 4-(1-hydroxy-3-butenyl)-(71787-53-6)
• EPA Substance Registry System: Benzonitrile, 4-(1-hydroxy-3-butenyl)-(71787-53-6)

Safety Data

• Hazardous Substances Data: 71787-53-6(Hazardous Substances Data)

Upstream product

• 762-73-2 trimethyl(allyl)stannane 
• 105-07-7 4-cyanobenzaldehyde 
• 107-05-1 3-chloroprop-1-ene 
• 556-56-9 allyl iodid 
• 106-95-6 allyl bromide 
• 591-87-7 Allyl acetate 
• 121598-69-4 4-(1-hydroxybut-3-yn-1-yl)benzonitrile 
• 107-37-9 allyltrichlorosilane 
• 1122-91-4 4-bromo-benzaldehyde 
• 7393-43-3 tetraallyl tin 
• 24850-33-7 allyltributylstanane 
• 107-18-6 allyl alcohol 
• 424819-51-2 allylgallium dichloride 
• 36971-15-0 3-isopropyl-2-methyl-hex-5-en-3-ol 

Downstream Products

• 71104-81-9 4-acetoxy-4-(p-cyanophenyl)-1-butene 
• 814-29-9 Tributylphosphine oxide 
• 227940-91-2 4-(1-{[1-(tert-butyl)-1,1-dimethylsilyl]-oxy}-3-butenyl)benzonitrile 
• 1033605-69-4 C₁₁H₁₀ClN 
• 959311-24-1 (E)-4-(but-2-enoyl)benzonitrile 
• 1620206-41-8 (E)-N-(1-bromo-4-(4-cyanophenyl)but-3-en-2-yl)-2,2,2-trichloroacetamide 
• 1620206-23-6 C₁₃H₁₁Cl₃N₂O 
• 116332-51-5 4-(1H-pyrrol-2-yl)benzonitrile 
• 1616603-26-9 C₁₃H₁₂N₂O₂ 
• 1403478-04-5 diethyl 1-((3-(4-4-cyanophenyl)-4,5-dihydroisoxazol-5-yl)methyl)hydrazine-1,2-dicarboxylate 
• 1403477-94-0 4-(5-(((2,2,6,6-tetramethylpiperidin-1-yl)oxy)methyl)-4,5-dihydroisoxazol-3-yl)benzonitrile 

Relevant articles and documents

Nickel-Catalyzed Reductive Allylation of Aldehydes with Allyl Acetates

Carbonyl allylation reactions constitute an important step in the formation of carbon-carbon reactions, and involve various related reactions that chiefly use allylmetal reagents. This report presents a nickel-catalyzed carbonyl allylation reaction using allyl acetate, which produces homoallyl alcohols in moderate to good yields, as an efficient methodology under reductive coupling conditions.

Copper-Impregnated Magnesium-Lanthanum Mixed Oxide: A Reusable Heterogeneous Catalyst for Allylation of Aldehydes and Ketones

Copper-impregnated magnesium-lanthanum mixed oxide [Cu(II)/Mg?La] was used as catalyst in synthesis of homoallylic alcohols from aldehydes and ketones using allyltributylstannane as the allylating source. The present protocol provides a great application

Cp2TiCl2-Catalyzed Photoredox Allylation of Aldehydes with Visible Light

A Barbier-type Cp2TiCl2-mediated (10 mol %) photoredox allylation of aldehydes under irradiation with visible light (blue light-emitting diodes (LEDs), 450 nm) and in the presence of an organic dye (3DPAFIPN, 5 mol %) with allylbromides is described.