Purity: 99% Excellent quality with competitive price Fast delivery Appearance:Colorless to light yellow oil liquid Storage:Store in cool dry place Package:drum packing Application:Used in food flavors,pharmaceutical intermediates. Port:Shangha
Cas:142-62-1
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Cas:142-62-1
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Cas:142-62-1
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inquiryItems Standard Result Appearance A clear intense yellow, viscous, oily liquid Conforms Assay ≥
Cas:142-62-1
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inquiryCaproic acid CAS RN: 142-62-1 Molecular formula: C6H12O2 Molecular weight: 116.16 Properties: Colorless to light yellow oily liquid with odor of cheese and swea
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High purity CAS 142-62-1 Hexanoic acid in stock Our main business covers the fields below: 1.Noble Metal Catalysts (Pt.Pd...) 2.Organic Phosphine Ligands (Tert-butyl-phosphine.Cyclohexyl-phosphine...) 3.OLED intermediates (Fluorene,Carb
Cas:142-62-1
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inquiryProduct Product name Hexanoic acid Synonyms Caproic acid CAS NO. 142-62-1 Molecu
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Cas:142-62-1
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inquirySuperior quality, moderate price & quick delivery. Appearance:colourless liquid Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:25kg/drum, or as per your request. Application:Used as Pharmaceutical Intermediat
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Cas:142-62-1
Min.Order:1 Gram
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Cas:142-62-1
Min.Order:1 Kilogram
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Type:Trading Company
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inquiryhigh purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:Foil bag; Drum; Plastic bottle Application:Pharma;Industry;Agricultural Transportation:by sea or air Port:any port in China
Conditions | Yield |
---|---|
With N-hydroxyphthalimide; trans-Re(O)Cl2(OC(CH3)2C(CH3)2O)2P(Ph)3; oxygen In acetonitrile at 30℃; under 760.051 Torr; for 1.1h; | 100% |
With diphenyl diselenide; dihydrogen peroxide In water at 20℃; for 3h; Green chemistry; | 99% |
With N-hydroxyphthalimide; oxygen In acetonitrile at 30℃; for 3h; Schlenk technique; | 99% |
Conditions | Yield |
---|---|
With air; potassium carbonate In water at 66.84℃; for 24h; | 100% |
With oxygen In water at 80℃; under 760.051 Torr; for 24h; | 99.3% |
Stage #1: hexan-1-ol With gold on titanium oxide In water at 90℃; for 0.166667h; Inert atmosphere; Stage #2: With dihydrogen peroxide In water at 90℃; for 1.08333h; Inert atmosphere; chemoselective reaction; | 99% |
hexanoyltrimethylsilane
hexanoic acid
Conditions | Yield |
---|---|
With ozone In dichloromethane at -78℃; | 99% |
potassium salt of 6-bromohexanoic acid
hexanoic acid
Conditions | Yield |
---|---|
With air; triethyl borane; bis{4-[2-(2-methoxyethoxy)ethoxy]phenyl}silane In tetrahydrofuran; water at 20℃; for 4h; Reduction; | 99% |
A
caprolactam
B
pentamide
C
5-hexenoic acid
D
hexanoic acid
E
valeric acid
Conditions | Yield |
---|---|
at 300℃; under 9000.9 Torr; for 5h; | A 99% B n/a C n/a D n/a E n/a |
Stage #1: caprolactam; 6-aminocaproic acid; 6-aminocaproic amide; nylon-6-oligomers; water; mixture of at 220℃; under 5250.53 - 52505.3 Torr; for 0.5h; Stage #2: at 300℃; under 9000.9 - 90009 Torr; for 5h; | A 99% B n/a C n/a D n/a E n/a |
Sb(C6H5)4(OOC(CH2)4CH3)
A
tetraphenylantimony(V) chloride
B
hexanoic acid
Conditions | Yield |
---|---|
With aq. HCl | A 99% B n/a |
Conditions | Yield |
---|---|
With water; zinc In acetonitrile at 25℃; for 3.5h; Sealed tube; Inert atmosphere; | 98% |
With water; zinc In acetonitrile at 80℃; for 4h; Inert atmosphere; Sealed tube; | 98% |
In n-heptane at 200℃; | 44% |
With N-ethyl-N,N-diisopropylamine In ethyl acetate; 1,2-dichloro-benzene |
n-hexanoic anhydride
2-Methylphenylboronic acid
A
1-(o-tolyl)hexan-1-one
B
hexanoic acid
Conditions | Yield |
---|---|
With P(p-CH3OC6H4)3; palladium diacetate In tetrahydrofuran; water at 60℃; for 16h; | A 98% B n/a |
Conditions | Yield |
---|---|
enzyme from Synechocystis sp. PCC 6803 In phosphate buffer at 30℃; for 12h; pH=7.2; | 97% |
With water; aluminum intercalated montmorillonite at 100℃; for 1h; Kinetics; microwave irradiation; | 40% |
With sulfuric acid |
hexylboronic acid
hexanoic acid
Conditions | Yield |
---|---|
With chromium(VI) oxide In dichloromethane; acetic acid at 25℃; for 12h; | 97% |
hexanoic acid
Conditions | Yield |
---|---|
With air; triethyl borane; bis[4-(2-hydroxyethoxy)phenyl]silane In tetrahydrofuran; water at 20℃; for 4h; Reduction; | 97% |
Conditions | Yield |
---|---|
With P(p-CH3OC6H4)3; palladium diacetate In tetrahydrofuran; water at 60℃; for 16h; | A n/a B 97% |
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; W(OTf)6; hydrogen at 135℃; under 760.051 Torr; for 12h; | 97% |
With palladium on activated carbon; W(OTf)6; hydrogen In neat (no solvent) at 135℃; under 760.051 Torr; for 12h; | 94% |
S-tert-butyl hexanethioate
hexanoic acid
Conditions | Yield |
---|---|
With lithium chloride In water; acetonitrile for 2h; Ambient temperature; electrolysis (undivided cell with platinum electrodes, 0.1 A constant current), other electrolytes, 1- and 2-propanol, or methanol instead of water; | 96% |
With lithium chloride In water; acetonitrile for 2h; Product distribution; Mechanism; Ambient temperature; electrolysis (undivided cell with platinum electrodes at a constant current of 0.1 A), other electrolyte, other solvents; (electrooxidative C-S-cleavage); | 96% |
S-tert-butyl hexanethioate
A
2-methylpropane-2-sulfinic acid
B
t-butylsulfonic acid
C
hexanoic acid
Conditions | Yield |
---|---|
With water; lithium bromide In acetonitrile electrolysis; further conditions: LiCl, electrolysis; | A n/a B n/a C 96% |
Conditions | Yield |
---|---|
With tricyclohexylphosphine; palladium diacetate In tetrahydrofuran; water at 60℃; for 16h; | A n/a B 96% |
5-hexanolide
hexanoic acid
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; W(OTf)6; hydrogen at 135℃; under 760.051 Torr; for 12h; | 96% |
With palladium on activated carbon; W(OTf)6; hydrogen In neat (no solvent) at 135℃; under 760.051 Torr; for 12h; | 96% |
With hydrogen; Al(OH)(2,2'-bipyridine-5,5'-dicarboxylic acid)0.81(PdCl2)0.48(OTf)0.38 In 1,2-dichloro-ethane at 130℃; under 15001.5 Torr; for 24h; Autoclave; | 55% |
Conditions | Yield |
---|---|
With nitric acid In dichloromethane at 0℃; for 2h; | A 60% B 95% |
n-hexanoic anhydride
phenylboronic acid
A
caprophenone
B
hexanoic acid
Conditions | Yield |
---|---|
With P(p-CH3OC6H4)3; palladium diacetate In tetrahydrofuran; water at 60℃; for 16h; | A 95% B n/a |
With palladium diacetate; triphenylphosphine In water; toluene at 55℃; for 3h; Inert atmosphere; Overall yield = 80.3 %; |
Conditions | Yield |
---|---|
With poly-4-vinylpyridine In N,N-dimethyl-formamide for 0.05h; microwave irradiation; | 94% |
In water for 0.25h; Decarboxylation; microwave irradiation; | 88% |
at 145℃; | |
With hydrogenchloride |
Conditions | Yield |
---|---|
Stage #1: carbon dioxide; n-pentylzinc bromide With [Ni(PCy3)2]2(N2) In tetrahydrofuran; toluene at 0℃; under 760.051 Torr; Inert atmosphere; Stage #2: With hydrogenchloride In tetrahydrofuran; water; ethyl acetate; toluene | 94% |
Conditions | Yield |
---|---|
With sodium hydroxide; sodium bromite; sodium bromide In water for 12h; Ambient temperature; | 93% |
(E)-oct-2-en-1-ol
hexanoic acid
Conditions | Yield |
---|---|
With potassium permanganate; H-montmorillonite In water; benzene at 25 - 30℃; for 1h; | 92% |
Conditions | Yield |
---|---|
With Na12(Ga4(1,5-bis(2,3-dihydroxybenzamido)naphthalene))6; [(DMPE)Rh(COD)][BF4]; hydrogen In aq. phosphate buffer at 20℃; for 20h; pH=8; Reagent/catalyst; | 92% |
With hydrogen; RhCl3 In benzene at 30℃; under 760 Torr; Rate constant; initial rate in the presence of 2-, 3- and 4-hexenoic acid; | |
With water; hydrogen; RhCl3 In benzene at 30℃; under 760 Torr; Rate constant; initial rate in the presence of 2-, 3- and 4-hexenoic acid; |
ethyl 3-oxo-2-(triphenylphosphoranylidene)octanoate
A
Triphenylphosphine oxide
B
hexanoic acid
Conditions | Yield |
---|---|
With sodium hydroxide; sodium hypochlorite In tetrahydrofuran at 25℃; for 4h; | A n/a B 92% |
dipentyl ketone
benzaldehyde
A
(E)-1-phenyl-1-hexene
B
hexanoic acid
Conditions | Yield |
---|---|
With boron trifluoride diacetate In hexane for 2.5h; Aldol-Grob reaction; Heating; | A n/a B 92% |
Conditions | Yield |
---|---|
With pyrographite; sodium hydroxide In water at 20℃; for 24h; Reagent/catalyst; Temperature; | 92% |
Multi-step reaction with 2 steps 1: 94 percent Chromat. / methyl iodide / toluene / 42 h / 90 - 115 °C 2: 12.3 g / H2O / 0.5 h View Scheme |
sodium caproate
hexanoic acid
Conditions | Yield |
---|---|
With hydrogenchloride In water | 92% |
Conditions | Yield |
---|---|
Product distribution; multistep reaction; via oxidation of a organoborane intermediate; other terminal alkenes; | 91% |
With chromium(VI) oxide; sodium tetrahydroborate; sulfuric acid; water; acetic acid; tert-butyl alcohol 1.) THF, a.) r.t., 2 h, b.) 50 deg C, 2 h, 2.) acetone, r.t., 10 h; Yield given. Multistep reaction; | |
Yield given. Multistep reaction; |
Conditions | Yield |
---|---|
Stage #1: 1-nitrohexane With potassium hydroxide In methanol Nef reaction; Continuous flow conditions; Stage #2: With potassium permanganate; disodium hydrogenphosphate; water In methanol at 25℃; for 0.166667h; Nef reaction; Sonication; Continuous flow conditions; Stage #3: With hydrogenchloride; sodium thiosulfate; sodium chloride In methanol; water; ethyl acetate | 91% |
With sodium hydroxide; disodium hydrogenphosphate; oxone 1.) MeOH, 1 h, 2.) room temperature, 1 h; Yield given. Multistep reaction; | |
Multi-step reaction with 2 steps 1: 56 percent / AcONH4 / acetic acid / 10 h / 100 °C 2: aq. H2O2; OH(-); 1-butyl-3-methylimidazolim trifluoromethanesulfonate / 16 h / 25 °C View Scheme |
Conditions | Yield |
---|---|
zirconium(IV) oxide for 5h; Heating; | 100% |
With 4-methyl-morpholine; 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride for 4h; | 93% |
With 8-hydroxyquinoline methanesulfonate at 85℃; for 3h; Temperature; Reagent/catalyst; Concentration; | 91.4% |
Conditions | Yield |
---|---|
With oxalyl dichloride In dichloromethane for 2h; | 100% |
With oxalyl dichloride In dichloromethane for 2.08333h; | 100% |
With thionyl chloride In toluene for 3h; Reflux; | 97.8% |
Conditions | Yield |
---|---|
With 18-crown-6 ether; potassium carbonate at 90 - 150℃; for 2h; | 100% |
2-methylmethoxybenzene
hexanoic acid
1-(4-methoxy-3-methylphenyl)-1-hexanone
Conditions | Yield |
---|---|
With tetrachlorosilane; 4-(trifluoromethyl)benzoic anhydride; silver perchlorate In dichloromethane for 24h; Ambient temperature; | 100% |
With tetrachlorosilane; 4-(trifluoromethyl)benzoic anhydride; silver perchlorate In dichloromethane for 24h; Ambient temperature; | 100% |
Conditions | Yield |
---|---|
Stage #1: hexanoic acid With dicyclohexyl-carbodiimide In dichloromethane for 0.25h; Inert atmosphere; Cooling with ice; Stage #2: methyl 9,10-dihydroxy stearate With dmap In dichloromethane at 20℃; for 14h; Cooling with ice; | 100% |
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0 - 20℃; for 16h; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
With Candida antarctica lipase; zinc(II) chloride In acetonitrile at 50℃; for 24h; | 99.8% |
With Candida antarctica lipase In acetonitrile at 50℃; for 24h; Kinetics; Product distribution; Further Variations:; Reaction partners; Reagents; Solvents; Temperatures; | 76.7% |
With Candida antarctica lipase In acetonitrile at 50℃; for 24h; Kinetics; | 76.7% |
Stage #1: 2,2'-iminobis[ethanol]; hexanoic acid With benzotriazol-1-ol; triethylamine In dichloromethane for 0.25h; Cooling with ice; Stage #2: With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; Cooling with ice; |
Conditions | Yield |
---|---|
With borane-ammonia complex In 5,5-dimethyl-1,3-cyclohexadiene for 6h; Reflux; | 99% |
With 1-methyl-pyrrolidin-2-one; 3,3'-(phenylphosphinylidene)bis<2(3H)-benzothiazolone; triethylamine for 2h; Ambient temperature; | 97% |
Stage #1: hexanoic acid With N-chlorobenzotriazole; triphenylphosphine In dichloromethane for 0.25h; Stage #2: benzylamine With triethylamine In dichloromethane at 20℃; for 1.16667h; | 92% |
Conditions | Yield |
---|---|
With thexylchloroborane-Me2SO4 In dichloromethane for 0.25h; Ambient temperature; | 99% |
With thexylchloroborane-Me2SO4 In dichloromethane for 0.25h; Product distribution; Ambient temperature; other aliphatic and aromatic acids, other products, other times; | 99% |
With thexylbromoborane dimethyl sulfide complex In carbon disulfide; dichloromethane at -20 - 20℃; for 1h; | 94% |
Conditions | Yield |
---|---|
With dicyclohexyl-carbodiimide In dichloromethane at 20℃; for 16h; | 99% |
With triethylamine; Phenyl N-phenylphosphoramidochloridate In dichloromethane for 0.75h; Ambient temperature; | 92% |
With N,N,N',N'-tetramethylchlorformamidinium chloride; triethylamine In dichloromethane at -30 - 0℃; for 5h; | 83% |
1-hydroxy-pyrrolidine-2,5-dione
hexanoic acid
hexanoic acid hydroxysuccinimide ester
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0 - 20℃; for 16h; Inert atmosphere; | 99% |
With dicyclohexyl-carbodiimide In 1,4-dioxane for 10h; 0 deg C to r.t.; | 74% |
With dicyclohexyl-carbodiimide In DMF (N,N-dimethyl-formamide) at 0℃; for 5h; | 74% |
benzyl 4-oxo-1-piperidinecarboxylate
hexanoic acid
Conditions | Yield |
---|---|
With lithium diisopropyl amide In tetrahydrofuran at -78 - 20℃; | 99% |
With n-butyllithium; diisopropylamine 1.) THF, 20 deg C, 20 min, 2.) THF, from -78 deg C to 20 deg C; Multistep reaction; |
Conditions | Yield |
---|---|
With sulfuric acid at 219.84℃; under 3.75038 Torr; Pressure; Temperature; | 99% |
With sulfonated graphene oxide In toluene at 110℃; for 6h; Catalytic behavior; Time; Reagent/catalyst; | 84% |
With toluene-4-sulfonic acid In toluene for 6h; Heating; |
oxalyl dichloride
N,O-dimethylhydroxylamine*hydrochloride
hexanoic acid
N-methoxy-N-methyl hexanamide
Conditions | Yield |
---|---|
Stage #1: oxalyl dichloride; hexanoic acid With N,N-dimethyl-formamide In dichloromethane at 20℃; for 1h; Stage #2: N,O-dimethylhydroxylamine*hydrochloride With pyridine In chloroform at 0 - 20℃; for 1h; | 99% |
Conditions | Yield |
---|---|
In di-isopropyl ether for 1.5h; Inert atmosphere; | 99% |
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