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trans 6-phenyl-5-hexenoic acid
6-phenylhexanic acid
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In ethyl acetate at 25℃; under 1551.4 Torr; for 1h; | 95% |
With platinum(IV) oxide; hydrogen In tetrahydrofuran at 20℃; for 1h; |
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; water; sodium hydrogencarbonate at 80℃; under 600.06 Torr; for 9h; Reagent/catalyst; Time; | 95% |
1-Diazo-6-phenylhexan-2-one
6-phenylhexanic acid
Conditions | Yield |
---|---|
With lithium perchlorate In acetonitrile at 26.85℃; Wolff rearrangement; Electrochemical reaction; | 94% |
With silver nanocluster In 1,4-dioxane; water at 60℃; | 92% |
Conditions | Yield |
---|---|
With [2,2]bipyridinyl; bis(1,5-cyclooctadiene)nickel (0); zinc In N,N-dimethyl acetamide at 80℃; for 12h; | 90% |
Conditions | Yield |
---|---|
With oxygen; vanadium(V) oxychloride In acetic acid at 65℃; for 52h; | 81% |
With potassium hydroxide In 5,5-dimethyl-1,3-cyclohexadiene Reflux; | 78% |
Conditions | Yield |
---|---|
With 10% rhodium on carbon; water; sodium hydroxide at 100℃; under 675.068 Torr; for 6h; Pressure; | A 11% B 80% |
Conditions | Yield |
---|---|
With indium; ammonium chloride In tetrahydrofuran for 24h; Heating; | A 60% B 27% |
6-oxo-6-phenyl-hexanoic acid methyl ester
6-phenylhexanic acid
Conditions | Yield |
---|---|
With hydrazine hydrate | 56% |
Multi-step reaction with 2 steps 1: aq. NaOH / acetone / 25 °C / other temp., ΔΔH excit., ΔΔS excit. View Scheme |
carbon dioxide
2-bromo-5-phenylpentane
6-phenylhexanic acid
Conditions | Yield |
---|---|
With rubidium carbonate; diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate; (4s,6s)-2,4,5,6-tetra(9H-carbazol-9-yl)isophthalonitrile; (6,6’-dimethyl-2,2'-bipyridine)nickel(II) dibromide In N,N-dimethyl-formamide at 10℃; under 750.075 Torr; for 20h; Schlenk technique; Sealed tube; Irradiation; | 52% |
6-phenyl-1-hexanol
A
pentylbenzene
B
6-phenylhexanic acid
C
1-pentenylbenzene
Conditions | Yield |
---|---|
With 10% rhodium on carbon; sodium hydroxide In water at 100℃; for 24h; Inert atmosphere; | A n/a B 50% C n/a |
The Benzenehexanoic acid, with the CAS registry number 5581-75-9, has the systematic name of 6-phenylhexanoic acid. It is a kind of white solid, and belongs to the product category of Aromatics Compounds. And the molecular formula of the chemical is C12H16O2.
The characteristics of Benzenehexanoic acid are as followings: (1)ACD/LogP: 3.23; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 2.43; (4)ACD/LogD (pH 7.4): 0.64; (5)ACD/BCF (pH 5.5): 26.85; (6)ACD/BCF (pH 7.4): 1; (7)ACD/KOC (pH 5.5): 217.74; (8)ACD/KOC (pH 7.4): 3.49; (9)#H bond acceptors: 2; (10)#H bond donors: 1; (11)#Freely Rotating Bonds: 6; (12)Polar Surface Area: 26.3 Å2; (13)Index of Refraction: 1.523; (14)Molar Refractivity: 55.89 cm3; (15)Molar Volume: 182.9 cm3; (16)Polarizability: 22.15×10-24cm3; (17)Surface Tension: 41.7 dyne/cm; (18)Density: 1.051 g/cm3; (19)Flash Point: 240.2 °C; (20)Enthalpy of Vaporization: 59.2 kJ/mol; (21)Boiling Point: 319.2 °C at 760 mmHg; (22)Vapour Pressure: 0.000144 mmHg at 25°C.
Preparation of Benzenehexanoic acid: This chemical can be prepared by 6-phenylhex-5-enoic acid. The reaction will need reagent H2, catalyst 5% Pd/C, and the menstruum ethyl acetate. The reaction time is 1 hour with temperature of 25°C and pressure of 1551.4Pa, and the yield is about 95%.
Uses of Benzenehexanoic acid: It can be used to produce 6-phenyl-hexanoic acid. This reaction will need reagent LiAlH4, and the menstruum diethyl ether. The reaction time is 4 hours with temperature of 25°C, and the yield is about 91%.
You should be cautious while dealing with this chemical. It irritates to eyes, respiratory system and skin. Therefore, you had better take the following instructions: Wear suitable gloves and eye/face protection, and if in case of contacting with eyes, rinse immediately with plenty of water and seek medical advice.
Addtionally, the following datas could be converted into the molecular structure:
(1)SMILES: O=C(O)CCCCCc1ccccc1
(2)InChI: InChI=1/C12H16O2/c13-12(14)10-6-2-5-9-11-7-3-1-4-8-11/h1,3-4,7-8H,2,5-6,9-10H2,(H,13,14)
(3)InChIKey: JTXZPQIXIXYMDY-UHFFFAOYAZ