20851-55-2

Basic information

• Product Name: 4-Hepten-1-ol
• Synonyms: 4-hepten-1-ol
• CAS NO: 20851-55-2
• Molecular Formula: C₇H₁₄O
• Molecular Weight: 114.19
• Mol File: 20851-55-2.mol

Chemical Properties

• Boiling Point: 174.4°C at 760 mmHg
• Flash Point: 68.9°C
• Appearance: /
• Density: 0.844g/cm³
• Vapor Pressure: 0.375mmHg at 25°C
• Refractive Index: 1.446
• PKA: 15.12±0.10(Predicted)
• CAS DataBase Reference: 4-Hepten-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Hepten-1-ol(20851-55-2)
• EPA Substance Registry System: 4-Hepten-1-ol(20851-55-2)

Safety Data

• Hazardous Substances Data: 20851-55-2(Hazardous Substances Data)

Usage

InChI:InChI=1/C7H14O/c1-2-3-4-5-6-7-8/h3-4,8H,2,5-7H2,1H3

Upstream product

• 138234-60-3 Hepten-3-saeure-ethylester 
• 98096-53-8 C₉H₂₁NO₂ 
• 6564-95-0 4-oxobutyl acetate 
• 6228-47-3 n-propyltriphenylphosphonium bromide 

Downstream Products

• 67114-38-9 5-(hex-3-en-1-yl)dihydrofuran-2(3H)-one 
• 6191-72-6 <(Z)-4-Heptenyl>-triphenylphosphonium-bromid 

Relevant articles and documents

Access to Saturated Thiocyano-Containing Azaheterocycles via Selenide-Catalyzed Regio-A nd Stereoselective Thiocyanoaminocyclization of Alkenes

An efficient route for the synthesis of saturated thiocyano-containing azaheterocycles by selenide-catalyzed regio-A nd stereoselective thiocyanoaminocyclization of alkenes is disclosed. The desired products were obtained in moderate to high yields under mild conditions. The generality of this method was elucidated by its efficient application in thiocyano oxycyclization of alkenes.

EVOLUTION THERMIQUE DE N-OXYDES DE DIMETHYLAMINO-5 ALCANOLS-1 SUBSTITUES EN 5. COMPETITION ENTRE REARRANGEMENTS DE COPE ET DE MEISENHEIMER

The effect of the substituent R in the 5 position was studied in the decomposition of 1,5-aminoalcohol N-oxides: Meisenheimer rearrangements takes place when R is the vinyl group but is not observed with the phenyl substituent; elimination to alkenol only