6398-51-2

Basic information

• Product Name: 4-(2-FURYL)-1-BUTEN-4-OL 97
• Synonyms: 4-(2-FURYL)-1-BUTEN-4-OL 97;2-FuranMethanol, a-2-propenyl-;α-2-propen-1-yl-2-FuranMethanol;1-(2-Furyl)-3-butenol;2-(1-Hydroxy-3-butenyl)furan;alpha-(2-Propenyl)-2-furanmethanol;alpha-Allylfurfuryl alcohol;NSC 75454
• CAS NO: 6398-51-2
• Molecular Formula: C₈H₁₀O₂
• Molecular Weight: 138.1638
• Mol File: 6398-51-2.mol
• Article Data: 155

Chemical Properties

• Boiling Point: 204-205 °C(lit.)
• Flash Point: 185 °F
• Appearance: /
• Density: 1.06 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.445mmHg at 25°C
• Refractive Index: n20/D 1.492(lit.)
• PKA: 13.89±0.20(Predicted)
• CAS DataBase Reference: 4-(2-FURYL)-1-BUTEN-4-OL 97(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(2-FURYL)-1-BUTEN-4-OL 97(6398-51-2)
• EPA Substance Registry System: 4-(2-FURYL)-1-BUTEN-4-OL 97(6398-51-2)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• WGK Germany: 2
• Hazardous Substances Data: 6398-51-2(Hazardous Substances Data)

Usage

General Description

4-(2-FURYL)-1-BUTEN-4-OL 97 is a chemical compound with the formula C8H10O2. It is a furan derivative with a 2-furyl group and a buten-4-ol chain. 4-(2-FURYL)-1-BUTEN-4-OL 97 is often used as a flavoring agent, imparting a sweet, sweet, burnt caramel and vanilla-like aroma to food and beverages. It is commonly found in many natural food sources, including coffee, baked goods, and cereal grains. Additionally, it is utilized in the production of fragrances and perfumes for its pleasant and unique scent. Furthermore, 4-(2-FURYL)-1-BUTEN-4-OL 97 is used in chemical synthesis as a versatile reagent for creating other organic compounds. Overall, this chemical compound has a wide range of applications in the food, fragrance, and chemical industries due to its distinctive flavor and aroma characteristics.

InChI:InChI=1/C8H10O2/c1-2-4-7(9)8-5-3-6-10-8/h2-3,5-7,9H,1,4H2

Upstream product

• 98-01-1 furfural 
• 1730-25-2 allylmagnesium bromide 
• 24850-33-7 allyltributylstanane 
• 132017-23-3 C₁₅H₃₂BrSb 
• 106-95-6 allyl bromide 
• 107-05-1 3-chloroprop-1-ene 
• 762-72-1 allyl-trimethyl-silane 
• 191732-48-6 (E)-(3-bromoprop-1-en-1-yl)tributylstannane 
• 113505-00-3 2-[(prop-2-en-1-yloxy)methyl]furan 
• 7393-43-3 tetraallyl tin 
• 108-24-7 acetic anhydride 
• 591-87-7 Allyl acetate 
• 107-37-9 allyltrichlorosilane 
• 72824-04-5 2-Allyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 

Downstream Products

• 119678-68-1 (R)-1-furan-2-yl-but-3-en-1-ol 
• 6398-51-2 (S)-1-(2-furyl)-3-buten-1-ol 
• 517907-50-5 (R)-(+)-1-(2-furyl)but-3-en-1-yl acetate 
• 1007313-65-6 2,4-bis-ethoxymethoxy-6-methyl-benzoic acid 1-furan-2-yl-but-3-enyl ester 
• 898552-02-8 (2S,6R)-2-Allyl-6-((2R,4aR,6S,7R,8aS)-7-hydroxy-4a-methyl-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-6-ylmethyl)-6-methoxy-6H-pyran-3-one 
• 898552-03-9 (2R,4aR,5aS,6aR,8S,10aS,11aR,12aS)-8-Allyl-6a-methoxy-4a-methyl-2-phenyl-decahydro-1,3,5,7,11-pentaoxa-naphthacen-9-one 
• 898552-05-1 (2R,4aR,5aS,6aR,8S,9S,10aS,11aR,12aS)-8-Allyl-6a-methoxy-4a-methyl-2-phenyl-dodecahydro-1,3,5,7,11-pentaoxa-naphthacen-9-ol 
• 898552-04-0 (2R,4aR,5aS,6aR,8S,9R,10aS,11aR,12aS)-8-Allyl-6a-methoxy-4a-methyl-2-phenyl-dodecahydro-1,3,5,7,11-pentaoxa-naphthacen-9-ol 
• 898552-00-6 (2S,6R)-2-Allyl-6-[(2R,4aR,6S,7R,8aS)-7-(tert-butyl-dimethyl-silanyloxy)-4a-methyl-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-6-ylmethyl]-6-methoxy-6H-pyran-3-one 
• 898551-97-8 (S)-1-{5-[(2R,4aR,6S,7R,8aS)-7-(tert-Butyl-dimethyl-silanyloxy)-4a-methyl-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-6-ylmethyl]-furan-2-yl}-but-3-en-1-ol 
• 634196-54-6 6-hydroxy-2-allyl-2H-pyran-3(6H)-one 

Relevant articles and documents

Nitrogen-Doped Carbon-Incarcerated Zinc Electrodes as Heterogeneous Catalysts for Electrochemical Allylation of Carbonyl Compounds

Electrochemical allylation reactions of carbonyl compounds using cathodes prepared from nitrogen-doped carbon (NDC)-incarcerated zinc catalysts have been developed. A range of aldehydes and ketones afforded the desired allylic alcohols in high yields with 10 mol % zinc leaching, and the heterogeneous nature of the active species was suggested. Compared with bulk zinc electrodes, NDC-stabilized zinc nanoparticle species were compatible with a broader range of heteroaromatic substrates and enabled the use of an undivided cell.

Indium-mediated allylation of carbonyl compounds in deep eutectic solvents

This study describes, for the first time, the in situ generation of indium organometallic reagents in environmentally friendly deep eutectic solvents (DESs). The allylation process of different carbonyl compounds is achieved mediated by indium metal and u

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.