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inquiryItems Standard Result Appearance Colorless to light yellow liquid Complies Assay 99%min
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inquiryProduct name 3-Methylbenzaldehyde Synonym M-Tolualdehyde CAS No 620-23-5 Molecular formula
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inquirySuperior quality, moderate price & quick delivery. Appearance:Colorless or beige liquid Storage:in shade Package:25kg/drum, or as per your request. Application:For medicine , pesticide intermediates Transportation:as per your request. Port:
Product name: 3-Methylbenzaldehyde CAS No.:620-23-5 Molecule Formula:C8H8O Molecule Weight:120.14 Purity: 99% Package: 200kg/drum Description:Colorless liquid Manufacture Standards:Enterprise Standard TESTING ITEMS
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inquirym-Tolualdehyde Chemical Properties Melting point <25 °C Boiling point 199 °C(lit.) density 1.019 g/mL at 25 °C(lit.) FEMA 3068 | TOLUALDEHYDES (MIXED O,M,P) refractive index n20/D 1.541(lit.) Fp 173 °F stora
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inquiryConditions | Yield |
---|---|
With triethylsilane; palladium diacetate; sodium hydrogencarbonate; sodium carbonate at 20℃; under 760.051 Torr; for 48h; | 90% |
With rhodium(III) chloride trihydrate; hydrogen; triethylamine; triphenylphosphine In N,N-dimethyl acetamide at 90℃; under 7500.75 Torr; for 12h; Autoclave; | 90% |
With sodium formate In N,N-dimethyl-formamide at 110℃; under 760.051 Torr; for 5h; | 86% |
With sodium formate In N,N-dimethyl-formamide at 100℃; under 760.051 Torr; for 10h; | 84% |
With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride In benzene at 110℃; under 66195.7 Torr; for 2h; | 68 % Chromat. |
3-methylbenzaldehyde oxime
m-tolyl aldehyde
Conditions | Yield |
---|---|
With N,N'-dichlorophenobarbital In acetonitrile at 20℃; | 95% |
With molybdenum(V) chloride; zinc In acetonitrile at 20℃; for 0.0833333h; | 94% |
With potassium permanganate; 1-n-butyl-3-methylimidazolim bromide at 20℃; for 1h; Ionic liquid; chemoselective reaction; | 91% |
1,1-diacetoxy-1-(3-methylphenyl)-methane
m-tolyl aldehyde
Conditions | Yield |
---|---|
With sulphated zirconia In acetonitrile at 60℃; for 0.3h; Microwave irradiation; | 100% |
With sulfonated rice husk ash In acetonitrile at 60℃; for 0.0333333h; | 91% |
With saccharin sulfonic acid at 90℃; for 0.05h; Neat (no solvent); | 90% |
Conditions | Yield |
---|---|
With dihydrogen peroxide In water; acetonitrile at 25℃; for 10h; UV-irradiation; | 92% |
With potassium 12-tungstocobaltate(III) In water; acetonitrile for 0.166667h; Microwave irradiation; | 90% |
With dipotassium peroxodisulfate In water at 90℃; for 12h; Green chemistry; | 80% |
With oxygen; copper diacetate In dimethyl sulfoxide at 120℃; for 18h; Sealed tube; | 71% |
With iron(III) chloride; oxygen In N,N-dimethyl-formamide at 110℃; | 67% |
Conditions | Yield |
---|---|
With dichloro [1,1'-bis(diphenylphosphino)propane]palladium(II); 1,8-diazabicyclo[5.4.0]undec-7-ene In N,N-dimethyl-formamide at 80℃; under 7500.75 Torr; for 20h; Autoclave; Green chemistry; | 86% |
With carbon supported Pd nanoparticles; 1,8-diazabicyclo[5.4.0]undec-7-ene In acetonitrile at 80℃; under 7500.75 Torr; for 12h; Sealed tube; Green chemistry; | 82% |
With rhodium(III) iodide; hydrogen; acetic anhydride; triethylamine; triphenylphosphine In N,N-dimethyl acetamide at 100℃; for 24h; Autoclave; | 80% |
Conditions | Yield |
---|---|
With iodine; triethylamine; triphenylphosphine In toluene at 80℃; Inert atmosphere; Sealed tube; | 81% |
With iodine; triethylamine; triphenylphosphine In toluene at 80℃; for 2h; Sealed tube; | 77% |
With palladium diacetate; triethylamine; dicyclohexyl-carbodiimide; tricyclohexylphosphine In N,N-dimethyl-formamide at 80℃; for 10h; Inert atmosphere; Sealed tube; | 67% |
Conditions | Yield |
---|---|
With water; sodium hydroxide at 20℃; for 0.05h; Microwave irradiation; | 98% |
With 4-methylmorpholine N-oxide; 1-ethyl-3-methyl-1H-imidazol-3-ium chloride; potassium iodide at 100℃; for 0.0333333h; Microwave irradiation; Ionic liquid; | 90% |
With 4-methylmorpholine N-oxide In tetrahydrofuran at 20℃; for 12h; Reflux; | 80% |
Conditions | Yield |
---|---|
With iodosylbenzene; Cl-CH2-PS supported 5-amino-1,10-phenanthroline-Ru In acetonitrile at 60℃; for 2h; | 100% |
Stage #1: 3-methylbenzyl alcohol With iron(III) chloride hexahydrate; oxygen; silica gel In toluene for 0.0833333h; Autoclave; Stage #2: With 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical In toluene at 80℃; under 3750.38 Torr; for 8h; Autoclave; | 99% |
With dihydrogen peroxide In water at 100℃; for 6.5h; chemoselective reaction; | 99% |
Conditions | Yield |
---|---|
With dipotassium hydrogenphosphate; fac-tris(2-phenylpyridinato-N,C2')iridium(III); tris-(trimethylsilyl)silane; dimethyl dicarbonate In acetonitrile at 20℃; for 6h; Schlenk technique; Inert atmosphere; Sealed tube; Irradiation; | 90% |
With potassium phosphate; sodium hypophosphite; 2,2-dimethylpropanoic anhydride; palladium diacetate; tricyclohexylphosphine In tetrahydrofuran at 60℃; for 16h; | 73% |
ueber <3-Methyl-α-phenylimino-benzyl>-phenyl-carbamidsaeure-aethylester; |
Conditions | Yield |
---|---|
With bis-triphenylphosphine-palladium(II) chloride; 2,2'-azobis(isobutyronitrile); oxygen; triethylamine In N,N-dimethyl-formamide at 110℃; under 760.051 Torr; for 4h; Schlenk technique; Sealed tube; | 63% |
Conditions | Yield |
---|---|
With formic acid; platinum(IV) oxide In water at 55 - 60℃; for 3h; | 92% |
With C13H26B(1-)*K(1+) In tetrahydrofuran for 24h; Ambient temperature; | 89% |
With diisobutylaluminium hydride In diethyl ether at 20℃; for 5h; | 76% |
Conditions | Yield |
---|---|
With bis-triphenylphosphine-palladium(II) chloride; 2,2'-azobis(isobutyronitrile); oxygen; triethylamine In N,N-dimethyl-formamide at 110℃; under 760.051 Torr; for 5h; Schlenk technique; Sealed tube; | 52% |
Conditions | Yield |
---|---|
With quinoline; Pd-BaSO4; xylene Hydrogenation; | |
With thexyl-s-butoxyborane In tetrahydrofuran at 25℃; for 120h; Yield given; | |
Multi-step reaction with 2 steps 1: 83 percent / pyridine / 0 °C 2: anhydrous potassium carbonate / methanol / 118 h / Heating View Scheme |
Conditions | Yield |
---|---|
With tetra-n-butylammonium peroxomonosulfate In dichloromethane at 20℃; for 0.5h; | |
With oxygen In water at 80℃; under 760.051 Torr; for 8h; | |
With Oxone In water at 50℃; for 21h; | |
With potassium peroxymonosulfate sulfate; tetrabutylammomium bromide In water at 70℃; for 4h; Reagent/catalyst; Green chemistry; |
Conditions | Yield |
---|---|
With bis-{4-methoxy-phenyl}-selenoxyde; sodium hydrogencarbonate In acetonitrile at 75℃; for 5h; | 93% |
With potassium hydrogencarbonate; dimethyl sulfoxide for 0.05h; Microwave irradiation; | 89% |
With hexamethylenetetramine durch Behandeln mit Wasser oder verd. Alkohol; | |
Multi-step reaction with 3 steps 1: 99 percent / Na2CO3 2: 99 percent / permaleic acid 3: 1.) trifluoroacetic anhydride; 2.) NBS / 1.) 10 min, r.t.; 2.) 80percent CH3CN, 20 min, r.t. View Scheme | |
With hexamethylenetetramine durch Behandeln mit Wasser oder verd. Alkohol; |
Conditions | Yield |
---|---|
With sodium tris(diethylamino)aluminum hydride In tetrahydrofuran; dodecane at -78℃; for 24h; | 89% |
With lithium-tris(diethylamino)hydridoaluminate In tetrahydrofuran at -78℃; for 3h; Reduction; | |
With Na(1+)*C12H27AlNO5(1-) In tetrahydrofuran; toluene at 0 - 20℃; for 0.5h; | 99 %Chromat. |
Conditions | Yield |
---|---|
With N,N,N,N,-tetramethylethylenediamine; hydrogen; palladium diacetate; propyl di-tert-butylphosphinite In toluene at 100℃; under 3750.38 Torr; for 20h; Inert atmosphere; | 89% |
With poly-γ-(p-diphenylphosphinophenyl)propylsiloxane Pd; sodium acetate In N,N-dimethyl-formamide at 110℃; for 12h; | 53% |
3-methylstyrene
A
3-methylstyrene oxide
B
m-tolyl aldehyde
Conditions | Yield |
---|---|
With [Cu(2,2'-bipyridine)(2-hap)(ClO4)]; dihydrogen peroxide In acetonitrile at 60℃; for 8h; | A 85% B n/a |
With tert.-butylhydroperoxide In acetonitrile at 65 - 68℃; for 24h; | A 63% B 23% |
With tert.-butylhydroperoxide; Gd2(N3)(nic)2(OH)3(Hnic)(H2O) In acetonitrile at 68 - 70℃; for 24h; | A 60% B 35% |
Conditions | Yield |
---|---|
With lithium diisobutylmorpholinoaluminum hydride In tetrahydrofuran; hexane at 0℃; for 0.5h; | 97 %Chromat. |
With benzoic acid ethyl ester; copper diisobutyl-t-butoxyaluminum hydride In tetrahydrofuran at 20℃; for 12h; Temperature; Solvent; Inert atmosphere; chemoselective reaction; | 95 %Chromat. |
With acetophenone In tetrahydrofuran at 0℃; for 0.5h; Inert atmosphere; | 33 %Chromat. |
(E)-3,3'-dimethylstilbene
m-tolyl aldehyde
Conditions | Yield |
---|---|
With iodine; oxygen; trifluoroacetic acid In methanol for 20h; Irradiation; | 83% |
Conditions | Yield |
---|---|
With carbon tetrabromide; oxygen In acetonitrile at 20℃; for 2.5h; Irradiation; Green chemistry; | 90% |
With 1,4-bis(triphenylphosphonium)butane cerium nitrate In water; acetic acid for 0.5h; Reflux; | 88% |
With 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione In fluorobenzene; dimethyl sulfoxide at 85℃; for 16h; | 85% |
3-methylbenzyl alcohol
aniline
A
N-(3-methylbenzylidene)aniline
B
N-(3-methylbenzyl)aniline
C
m-tolyl aldehyde
Conditions | Yield |
---|---|
With PdAu alloy nanoparticles encapsulated inside MIL-100(Fe) cavities In acetonitrile for 24h; Irradiation; Inert atmosphere; Schlenk technique; Sealed tube; | A 14% B 77% C 36% |
With Pd nanoparticles encapsulated inside a MIL100(Fe) cavity In acetonitrile for 24h; Sealed tube; Irradiation; Inert atmosphere; | A 16% B 62% C 24% |
2-(m-tolyl)-1,3-dithiolane
m-tolyl aldehyde
Conditions | Yield |
---|---|
With silica gel; ferric nitrate In hexane at 50℃; for 0.166667h; | 98% |
With indium (III) iodide; dihydrogen peroxide In water; toluene at 20℃; for 15h; Inert atmosphere; Sealed tube; | 82 mg |
Conditions | Yield |
---|---|
With rhodium(III) iodide; dichloro [1,1'-bis(diphenylphosphino)propane]palladium(II); hydrogen; acetic anhydride; triethylamine; triphenylphosphine In N,N-dimethyl acetamide at 100℃; for 24h; Autoclave; | 90% |
With dichloro [1,1'-bis(diphenylphosphino)propane]palladium(II); 1,8-diazabicyclo[5.4.0]undec-7-ene In N,N-dimethyl-formamide at 100℃; under 7500.75 Torr; for 20h; Autoclave; Green chemistry; | 76% |
m-xylene
A
3-methylbenzyl alcohol
B
m-tolyl aldehyde
C
m-Toluic acid
Conditions | Yield |
---|---|
With zinc(II) 1,8,15,22-tetrachlorophthalocyanine; C60H60BrFeN4; oxygen; nickel diacetate at 125℃; under 4500.45 - 7500.75 Torr; for 1.5h; Reagent/catalyst; Pressure; Temperature; | |
Stage #1: m-xylene at 220℃; under 18001.8 Torr; Stage #2: With water at 182℃; under 12001.2 Torr; | |
With [(copper(II))3(μ3-1κN3,2κN2O,3κN-N′-(di(pyridin-2-yl)methylene)pyrazine-2-carbohydrazide)(μ-nitrate)(nitrate)3(H2O)3]*(nitrate); dihydrogen peroxide In acetonitrile at 50℃; for 3h; Time; Reagent/catalyst; Microwave irradiation; | A 15.3 %Chromat. B 5.9 %Chromat. C 3.4 %Chromat. |
1-(3'-methylphenyl)-1,2-dihydroxyethane
m-tolyl aldehyde
Conditions | Yield |
---|---|
With oxygen; sodium carbonate In water at 20℃; for 5h; Irradiation; Green chemistry; | 79% |
2-(3-methylphenyl)-1,3-dithiane
m-tolyl aldehyde
Conditions | Yield |
---|---|
Stage #1: 2-(3-methylphenyl)-1,3-dithiane With trichloroisocyanuric acid; silica gel at 20℃; for 0.05h; Stage #2: With water at 20℃; | 94% |
With tetrachlorosilane; dimethyl sulfoxide In dichloromethane at 20℃; for 0.583333h; | 93% |
Conditions | Yield |
---|---|
In ethanol Heating; | 100% |
In benzene Heating; |
Conditions | Yield |
---|---|
at 20℃; for 12h; | 100% |
In methanol at 25℃; Mechanism; Rate constant; Thermodynamic data; ΔH(excit.), ΔS(excit.), kinetic solvent isotope effect; | |
With sodium sulfate In dichloromethane for 2h; |
Conditions | Yield |
---|---|
(1S)-1-(9-piperidylfluoren-9-yl)ethanol In hexane; toluene at 0℃; for 4h; Addition; | 100% |
Stage #1: diethylzinc With 2,2'-(propane-2,2-diyl)bis(6,6-dimethyl-5,6,7,8-tetrahydro-5,7-methanoquinoline-8,2-diyl)bis(diphenylmethanol) In toluene at 20℃; for 0.166667h; Inert atmosphere; Stage #2: m-tolyl aldehyde In toluene at -20℃; for 57h; Inert atmosphere; enantioselective reaction; | 95% |
Stage #1: m-tolyl aldehyde With (E,4R,5S)-N-allyl-5-cyclohexyl-5-hydroxy-4-morpholinopent-2-enamide In toluene at 20℃; for 0.333333h; Inert atmosphere; Stage #2: diethylzinc In hexane; toluene at 20℃; for 6h; Reagent/catalyst; Inert atmosphere; enantioselective reaction; | 95% |
Conditions | Yield |
---|---|
Stage #1: diethylzinc; m-tolyl aldehyde With (1S,2R,3S,5S)-6,6-dimethyl-2-morpholinobicyclo[3.1.1]heptan-3-ol; (1R,2S,3R,5R)-6,6-dimethyl-2-morpholinobicyclo[3.1.1]heptan-3-ol In hexane at -15 - 0℃; for 18h; Inert atmosphere; Stage #2: With water; ammonium chloride In hexane at 0℃; optical yield given as %ee; enantioselective reaction; | 100% |
With 4-methyl-N-{[(1S,2S)-2-(pyrrolidin-1-yl)cyclohexyl]methyl}benzenesulfonamide In hexane at 0℃; for 24h; Inert atmosphere; optical yield given as %ee; enantioselective reaction; | 97% |
With titanium(IV) isopropylate In dichloromethane at 0℃; | 96% |
1-amino-2-propene
m-tolyl aldehyde
Allyl-[1-m-tolyl-meth-(E)-ylidene]-amine
Conditions | Yield |
---|---|
With magnesium sulfate In dichloromethane at 20℃; for 20h; | 100% |
With 3 A molecular sieve In benzene at 65℃; |
Conditions | Yield |
---|---|
With potassium hydroxide In acetonitrile at 20℃; for 4h; Darzens condensation; | 100% |
With potassium hydroxide In dichloromethane at 20℃; Darzens condensation; | 76% |
Conditions | Yield |
---|---|
at 20℃; for 12h; | 100% |
at 20℃; for 1h; | |
In benzene for 2h; Reflux; |
Conditions | Yield |
---|---|
In methanol at 20℃; Molecular sieve; | 100% |
In methanol at 20℃; Molecular sieve; |
m-tolyl aldehyde
trimethyl orthoformate
1,1-dimethoxy-1-(3-methylphenyl)methane
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In methanol at 20℃; for 18h; | 100% |
With Pd(PhCN)2(OTf)2 at 20℃; for 0.5h; Inert atmosphere; | 91% |
With toluene-4-sulfonic acid In methanol at 20℃; for 2h; Molecular sieve; |
Conditions | Yield |
---|---|
Stage #1: N-prenyl-N-propargyltosylamide With ethylmagnesium bromide In tetrahydrofuran at 50℃; for 1h; Stage #2: m-tolyl aldehyde In tetrahydrofuran at 20℃; for 3h; | 100% |
Stage #1: N-prenyl-N-propargyltosylamide With ethylmagnesium bromide In tetrahydrofuran at 50℃; for 1h; Stage #2: m-tolyl aldehyde In tetrahydrofuran at 20℃; for 3h; |
dimethyl (2-oxo-2-(1H-pyrrol-1-yl)ethyl)phosphonate
m-tolyl aldehyde
(E)-1-(1H-pyrrol-1-yl)-3-(m-tolyl)prop-2-en-1-one
Conditions | Yield |
---|---|
Stage #1: dimethyl (2-oxo-2-(1H-pyrrol-1-yl)ethyl)phosphonate With N-ethyl-N,N-diisopropylamine; lithium chloride In acetonitrile at 0℃; for 0.333333h; Stage #2: m-tolyl aldehyde In acetonitrile at 20℃; for 15h; | 100% |
1,3-dimethylbarbituric acid
diethylamine
m-tolyl aldehyde
5,5'-(3-tolylmethylene)bis(1,3-dimethylpyrimidine-2,4,6(1H,3H,5H)-trione) diethylaminium salt
Conditions | Yield |
---|---|
In water at 20℃; Inert atmosphere; | 100% |
With water; dimedone at 20℃; Green chemistry; | 97% |
Conditions | Yield |
---|---|
In water at 20℃; Inert atmosphere; | 100% |
1-ethyl-4-ethynylbenzene
m-tolyl aldehyde
1-(4′-methylphenyl)isoquinoline
Conditions | Yield |
---|---|
With palladium diacetate; sodium carbonate; triphenylphosphine In toluene at 80℃; for 2h; Inert atmosphere; | 100% |
1-ethyl-4-ethynylbenzene
m-tolyl aldehyde
Conditions | Yield |
---|---|
Stage #1: 1-ethyl-4-ethynylbenzene With n-butyllithium In tetrahydrofuran at -78℃; for 0.5h; Inert atmosphere; Stage #2: m-tolyl aldehyde In tetrahydrofuran at -78℃; for 3h; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
With magnesium sulfate In dichloromethane at 20℃; for 15h; Inert atmosphere; | 100% |
trimethyl phosphonoacetate
m-tolyl aldehyde
(E)-methyl 3-methylcinnamate
Conditions | Yield |
---|---|
Stage #1: trimethyl phosphonoacetate With sodium hydride In tetrahydrofuran; paraffin oil at 0 - 20℃; for 0.5h; Inert atmosphere; Stage #2: m-tolyl aldehyde In tetrahydrofuran; paraffin oil at -78 - 20℃; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
With alumina; isopropyl alcohol at 180℃; under 11251.1 Torr; for 0.666667h; Microwave irradiation; Sealed tube; | 99% |
With Candida boidinii formate dehydrogenase; Geobacillus stearothermophilus ε‐deaminating L‐lysine dehydrogenase variant 27; nicotinamide adenine dinucleotide In aq. buffer at 30℃; for 24h; pH=7; Reagent/catalyst; Enzymatic reaction; | 99% |
With triethylamine; isopropyl alcohol; lithium bromide at 20℃; for 48h; Meerwein-Ponndorf-Verley reaction; | 98% |
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