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Cas:143-07-7
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inquiryUnique advantages for Lauric acid Cas 143-07-7 Guaranteed the purity High quality & competitive price Quality control Fast feedback Prompt shipment Appearance:Liquid Storage:Store below +30°C Package:200kg/drum Application:Food Transport
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inquiryCompany Name: Hefei TNJ Chemical Industry Co.,Ltd. Registered Address: B911 Xincheng Business Center,South of Dongliu Road, Zhengwu District, Hefei, Anhui,China
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ProName: Cycloheptane-1,3-Dione CasNo: 1194-18-9 Molecular Formula: C7H10O2 Appearance: Look at the detailed information Application: intermediates DeliveryTime: according to the clients requirement PackAge: according to
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Lauric acid Basic information Product Name: Lauric acid Synonyms: Emery651;Hen-decane-1-carbosylicacid;Hydrofol acid 1255;Hydrofol acid 1295;hydrofolacid1255;hydrof
Cas:143-07-7
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inquiryProduct Description Product website: http://www.finerchem.com Product Name Lauric acid CAS No. 143-07-7 App
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inquiryLauric acid Lauric acid CAS NO 143-07-7 Appearance White crystalline powder Assay 99.0-101.0% Grade Pharmaceutical grade
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inquiryProduct Name: Lauric acid CAS: 143-07-7 MF: C12H24O2 MW: 200.32 EINECS: 205-582-1 Mol File: 143-07-7.mol Lauric acid Structure Lauric acid Chemical Properties Melting point 44-46 °C (lit.) Boiling point 225 °C/100
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Cas:143-07-7
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inquiryConditions | Yield |
---|---|
With air; sodium nitrite In trifluoroacetic acid at 0 - 20℃; for 5h; | 100% |
With Iron(III) nitrate nonahydrate; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; potassium chloride; oxygen In 1,2-dichloro-ethane at 25℃; for 12h; | 100% |
With Iron(III) nitrate nonahydrate; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; potassium chloride; oxygen In 1,2-dichloro-ethane at 20℃; for 12h; Reagent/catalyst; Schlenk technique; | 100% |
S-tert-butyl dodecanethioate
lauric acid
Conditions | Yield |
---|---|
With water; hydrophobic polystyrene-supported sulfonic acid for 168h; Heating; | 100% |
3-oxo-2-phenylsulfanyltetradecanamide
lauric acid
Conditions | Yield |
---|---|
With sodium hydrogencarbonate; 2-oxopropanal In methanol; water at 20℃; for 1h; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
With aluminum tri-bromide; ethanethiol for 0.5h; Ambient temperature; | 99.2% |
With magnesium iodide In toluene for 48h; Heating; | 70% |
Conditions | Yield |
---|---|
With iron oxide; oxygen; ethyl acetoacetate at 75 - 80℃; under 760.051 Torr; for 24h; Green chemistry; | 99% |
With oxygen; copper(II) acetate monohydrate; cobalt(II) diacetate tetrahydrate In water at 40℃; under 760.051 Torr; for 3h; | 97% |
With Iron(III) nitrate nonahydrate; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; potassium chloride; oxygen In 1,2-dichloro-ethane at 25℃; for 12h; | 94% |
Conditions | Yield |
---|---|
With sodium hypochlorite; sodium hydrogencarbonate; potassium bromide; [4-(TEMPO-4-yloxymethyl)-1H-[1,2,3]triazol-1-ylmethyl]-PS In dichloromethane at 0℃; for 0.5h; | A n/a B 99% |
With C30H24N2O7W; dihydrogen peroxide In water; acetonitrile for 22h; Reflux; | A 1% B 82% |
With 2,2,6,6-tetramethyl-piperidine-N-oxyl; oxone; potassium bromide; methyltrioxorhenium(VII) In acetonitrile at 0℃; for 4h; | A 6% B 53% |
Conditions | Yield |
---|---|
In d(4)-methanol at 20℃; Conversion of starting material; light irradiation; | A 99% B n/a |
Conditions | Yield |
---|---|
Stage #1: bromobutyric acid With 1-methyl-pyrrolidin-2-one; tert-butylmagnesium chloride In tetrahydrofuran at -78℃; for 0.166667h; Inert atmosphere; Stage #2: n-octylmagnesium chloride With buta-1,3-diene; nickel dichloride In tetrahydrofuran under 760.051 Torr; for 1h; Inert atmosphere; Cooling with ice; | 99% |
Conditions | Yield |
---|---|
With aluminum tri-bromide; ethanethiol for 48h; Ambient temperature; | 98.7% |
With AlBrCl3(1-)*C5H5N*H(1+) at 140℃; for 3h; | 98% |
With iodine; aluminium In acetonitrile at 80℃; for 18h; | 97% |
S-phenyl dodecanethioate
lauric acid
Conditions | Yield |
---|---|
With water; hydrophobic polystyrene-supported sulfonic acid for 24h; Heating; | 98% |
Conditions | Yield |
---|---|
With sodium hydroxide In ethanol for 1h; Reflux; | 98% |
With aquivion perfluorosulfonic superacid loaded on H+ In neat (no solvent) at 100℃; under 760.051 Torr; for 8h; Reagent/catalyst; |
Conditions | Yield |
---|---|
With AlBrCl3(1-)*C5H5N*H(1+) at 140℃; for 3h; | 97% |
With 2C33H37N*H2O7S2; water at 60℃; for 20h; | 83% |
With aluminum tri-bromide; ethanethiol for 792h; Ambient temperature; | 73.5% |
With 2C33H37N*H2O7S2; water at 80℃; | 83 %Spectr. |
With Novozym 435 from Candida antarctica at 0 - 40℃; for 32h; |
lauric acid
Conditions | Yield |
---|---|
With iodine In cyclohexane for 6h; Ambient temperature; | 97% |
Conditions | Yield |
---|---|
With C18-alkylated polystyrene-supported sulfonic acid; water for 24h; Heating; | A 96% B n/a |
With water; hydrophobic polystyrene-supported sulfonic acid for 72h; Heating; | A 95% B 95% |
With C18-alkylated polystyrene-supported sulfonic acid; water for 24h; Heating; |
S-dodecyl dodecanethioate
A
lauric acid
B
didodecyl sulfide
C
1-dodecylthiol
Conditions | Yield |
---|---|
With water; hydrophobic polystyrene-supported sulfonic acid for 72h; Heating; | A 95% B 2% C n/a |
Conditions | Yield |
---|---|
With tert.-butylnitrite; water at 29℃; for 0.583333h; | 95% |
lauric acid
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; W(OTf)6; hydrogen at 135℃; under 760.051 Torr; for 12h; | 94% |
With palladium on activated carbon; W(OTf)6; hydrogen In neat (no solvent) at 135℃; under 760.051 Torr; for 12h; | 94% |
Conditions | Yield |
---|---|
With water; hydrophobic polystyrene-supported sulfonic acid for 36h; Heating; | 93% |
Conditions | Yield |
---|---|
With hydrogen In ethanol; water at 240℃; under 25066.7 Torr; for 144h; | A 6% B 93% |
2-chloroethyl dodecanoate
lauric acid
Conditions | Yield |
---|---|
With sodium tetrahydroborate; selenium In N,N-dimethyl-formamide for 3h; Ambient temperature; also with NaHTe as cat.; | 92% |
2,2,2-Trichloroethyl dodecanoate
lauric acid
Conditions | Yield |
---|---|
With sodium tetrahydroborate; selenium In N,N-dimethyl-formamide at 40 - 50℃; for 1h; | 92% |
Conditions | Yield |
---|---|
With 2C33H37N*H2O7S2; water at 60℃; for 24h; | 92% |
With 2C33H37N*H2O7S2; water at 80℃; | 92 %Spectr. |
benzyl dodecanoate
toluene
A
lauric acid
B
1-methyl-3-(phenylmethyl)-benzene
C
1-methyl-4-(phenylmethyl)benzene
D
2-benzyltoluene
Conditions | Yield |
---|---|
With boron trifluoride diethyl etherate; water at 80℃; for 2h; regioselective reaction; | A 92% B n/a C n/a D n/a |
Conditions | Yield |
---|---|
With [2,2]bipyridinyl; bis(1,5-cyclooctadiene)nickel (0); zinc In N,N-dimethyl acetamide at 80℃; for 12h; | 92% |
lauric anhydride
phenylboronic acid
A
lauric acid
B
dodecanophenone
Conditions | Yield |
---|---|
With P(p-CH3OC6H4)3; palladium diacetate In tetrahydrofuran; water at 60℃; for 16h; | A n/a B 90% |
Conditions | Yield |
---|---|
With H2SO4*2NH2OH; Rh(OH)x/Al2O3 In water for 9h; Heating; | A 6 % Chromat. B 89% C 5 % Chromat. |
Conditions | Yield |
---|---|
With Oxone; 2-iodo-3,4,5,6-tetramethylbenzoic acid In water; acetonitrile for 24h; | 86% |
With Oxone In water; acetonitrile for 24h; Reflux; | 61% |
With sodium permanganate In hexane at 69℃; for 24h; | 13% |
Conditions | Yield |
---|---|
With oxygen; lithium bromide In ethyl acetate at 20℃; for 6h; UV-irradiation; | A 7% B 86% |
B
5-hydroxy-4-methyl-3-phenylsulfanyl-3-pyrrolin-2-one
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In tetrahydrofuran; water at 20℃; for 24h; Inert atmosphere; | A 86% B 7.8 mg C 18.2 mg D 2.5 mg E 2.3 mg |
thiophenol
(1R,5R)-1-dodecanoyl-4-hydroxy-4-methyl-6-oxa-3-azabicyclo[3.1.0]hexan-2-one
A
lauric acid
B
3-oxo-2-phenylsulfanyltetradecanamide
C
diphenyldisulfane
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In methanol; water at 20℃; for 0.5h; Inert atmosphere; | A 20% B 9% C 85% |
Conditions | Yield |
---|---|
With boron trifluoride at 65℃; for 0.333333h; | 100% |
With ethenetetracarbonitrile for 48h; Ambient temperature; | 99% |
polyaniline hydrocloride at 70℃; for 24h; | 99% |
Conditions | Yield |
---|---|
With thionyl chloride In N,N-dimethyl-formamide at 78℃; for 3h; | 100% |
With thionyl chloride; N,N-dimethyl-formamide at 88℃; for 2h; | 99% |
With thionyl chloride; sodium dodecanoylglycinate at 25℃; for 6h; Reagent/catalyst; Inert atmosphere; | 99.8% |
Conditions | Yield |
---|---|
With pyridine; phenylsulphur trifluoride; hydrogen fluoride at 50℃; for 24h; Product distribution / selectivity; Neat (no solvent); | 100% |
With phenylsulphur trifluoride at 20 - 100℃; for 2h; Product distribution / selectivity; Neat (no solvent); | 83% |
With 4-tert-butyl-2,6-dimethylphenylsulfur trifluoride at 100℃; for 2h; Reactivity; | 55% |
Conditions | Yield |
---|---|
With dicyclohexyl-carbodiimide In dichloromethane for 24h; | 100% |
With N-(3-dimethylaminopropyl)-N-ethylcarbodiimide In dichloromethane for 3h; | 98% |
With dicyclohexyl-carbodiimide In ethyl acetate for 6h; | 98% |
Conditions | Yield |
---|---|
With dodecylbenzene-sulphonic acid In water at 40℃; for 48h; | 100% |
With para-dodecylbenzenesulfonic acid In water at 40℃; for 48h; | 99% |
With triphenylphosphine-sulfur trioxide adduct In neat (no solvent) at 110℃; for 2h; Green chemistry; | 82% |
lauric acid
Conditions | Yield |
---|---|
With camphor sulphuric acid for 18h; Heating; | 100% |
lauric acid
2-chloro-1,3-dimethylimidazolinium chloride
A
1,3-dimethyl-2-imidazolidinone
B
n-dodecanoyl chloride
Conditions | Yield |
---|---|
In toluene | A 94% B 100% |
lauric acid
2-chloro-1,3-dimethylimidazolinium chloride
n-dodecanoyl chloride
Conditions | Yield |
---|---|
In toluene | 100% |
Conditions | Yield |
---|---|
With sodium hydrogencarbonate; 2-oxopropanal In methanol; water at 20℃; for 1h; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
In isopropyl alcohol for 1.5h; Product distribution / selectivity; | 100% |
Conditions | Yield |
---|---|
In water at 20℃; | 100% |
In water at 100℃; for 24h; |
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 40℃; for 1h; | 100% |
lauric acid
levobupivacaine
Conditions | Yield |
---|---|
In acetonitrile at 50℃; for 6h; | 100% |
Conditions | Yield |
---|---|
With sodium hypochlorite; sodium hydrogencarbonate; potassium bromide; [4-(TEMPO-4-yloxymethyl)-1H-[1,2,3]triazol-1-ylmethyl]-PS In dichloromethane at 0℃; for 0.5h; | A n/a B 99% |
With C30H24N2O7W; dihydrogen peroxide In water; acetonitrile for 22h; Reflux; | A 1% B 82% |
With 2,2,6,6-tetramethyl-piperidine-N-oxyl; oxone; potassium bromide; methyltrioxorhenium(VII) In acetonitrile at 0℃; for 4h; | A 6% B 53% |
(4-oxo-3-phenyl-4H-1,1-dioxothiochromen-2-yl)methyl dodecanoate
A
lauric acid
B
C16H10O3S
Conditions | Yield |
---|---|
In d(4)-methanol at 20℃; Conversion of starting material; light irradiation; | A 99% B n/a |
Conditions | Yield |
---|---|
Stage #1: bromobutyric acid With 1-methyl-pyrrolidin-2-one; tert-butylmagnesium chloride In tetrahydrofuran at -78℃; for 0.166667h; Inert atmosphere; Stage #2: n-octylmagnesium chloride With buta-1,3-diene; nickel dichloride In tetrahydrofuran under 760.051 Torr; for 1h; Inert atmosphere; Cooling with ice; | 99% |
lauric acid
Conditions | Yield |
---|---|
With tert.-butylnitrite; water at 29℃; for 0.583333h; | 95% |
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; W(OTf)6; hydrogen at 135℃; under 760.051 Torr; for 12h; | 94% |
With palladium on activated carbon; W(OTf)6; hydrogen In neat (no solvent) at 135℃; under 760.051 Torr; for 12h; | 94% |
ethyl dodecanethionate
lauric acid
Conditions | Yield |
---|---|
With water; hydrophobic polystyrene-supported sulfonic acid for 36h; Heating; | 93% |
ethyl 7-(5-methyltetrahydrothran-2-yl)-5-oxoheptanoate
ethyl 5-hydroxy-7-(5-methyltetrahydrothran-2-yl)heptanoate
A
lauric acid
B
ethyl laurate
Conditions | Yield |
---|---|
With hydrogen In ethanol; water at 240℃; under 25066.7 Torr; for 144h; | A 6% B 93% |
Conditions | Yield |
---|---|
With oxygen; lithium bromide In ethyl acetate at 20℃; for 6h; UV-irradiation; | A 7% B 86% |
methanol
3-oxo-2-phenylsulfanyltetradecanamide
2-oxopropanal
A
lauric acid
B
5-hydroxy-4-methyl-3-phenylsulfanyl-3-pyrrolin-2-one
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In tetrahydrofuran; water at 20℃; for 24h; Inert atmosphere; | A 86% B 7.8 mg C 18.2 mg D 2.5 mg E 2.3 mg |
lauric acid
pregabilin
(S)-3-(aminomethyl)-5-methylhexanoic acid laurate
Conditions | Yield |
---|---|
In isopropyl alcohol for 1.5h; Product distribution / selectivity; | 100% |
lauric acid
cholinium hydrogen carbonate
2-hydroxyethyltrimethylammonium laurate
Conditions | Yield |
---|---|
In water at 20℃; | 100% |
In water at 100℃; for 24h; |
Conditions | Yield |
---|---|
Stage #1: Fmoc-glycine-2-chlorotrityl resin With piperidine In N,N-dimethyl-formamide 2-Cl-Trt-Resin; Stage #2: N-(fluoren-9-ylmethoxycarbonyl)glycine With benzotriazol-1-ol; diisopropyl-carbodiimide In N,N-dimethyl-formamide at 20℃; for 1h; 2-Cl-Trt-Resin; Stage #3: lauric acid; Fmoc-Lys-OH Further stages; | 100% |
Conditions | Yield |
---|---|
In cyclohexane at 40℃; Solvent; | 100% |
Conditions | Yield |
---|---|
With zirconium(IV) oxychloride In 1,3,5-trimethyl-benzene at 162℃; for 24h; | 99.9% |
With choline chloride; zinc(II) chloride at 110℃; for 8h; | 99% |
lipase In hexane for 4h; | 94% |
lauric acid
trichlorovinylsilane
Octanoic acid
n-tetradecanoic acid
C36H68O6Si
Conditions | Yield |
---|---|
In toluene at 60 - 150℃; for 4h; | 99.82% |
lauric acid
copper
copper(II) laurate
Conditions | Yield |
---|---|
With ammonium acetate In ethanol; water at 27℃; for 4h; Concentration; Reagent/catalyst; Electrochemical reaction; | 99.69% |
Conditions | Yield |
---|---|
With Amberlyst 15 ion exchange resin In ethanol; water at 60℃; for 3h; Temperature; | 99.2% |
With sulfuric acid | |
With sulfuric acid at 40℃; | |
With lipase from Candida antarctica type B (Chirazyme(R) L-2 C2) In acetone at 50℃; | |
With Chirazyme(R) L-2 C2 In acetone at 55℃; for 24h; |
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