DayangChem exported this product to many countries and regions at best price. If you are looking for the material's manufacturer or supplier in China, DayangChem is your best choice. Pls contact with us freely for getting detailed product spe
Cas:529-23-7
Min.Order:1 Kilogram
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Min.Order:1 Gram
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Min.Order:5 Kiloliter
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inquiryTIANFUCHEM--529-23-7--2-Aminobenzaldehyde factory price Our company was built in 2009 with an ISO certificate.In the past 10 years, we have grown up as a famous fine chemicals supplier in China And we had established stable business rel
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Min.Order:1 Metric Ton
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Min.Order:1 Kilogram
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Type:Lab/Research institutions
inquiry2-Aminobenzaldehyde CAS:529-23-7 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality organic interm
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Min.Order:1 Gram
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Min.Order:1 Kilogram
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Hangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det
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Min.Order:0 Metric Ton
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Min.Order:1 Gram
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2-Aminobenzaldehyde Chemical Properties Melting point 38°C Boiling point 225.84°C (rough estimate) density 1.1344 (rough estimate) refractive index 1.5323 (estimate) Fp 113 °C storage temp. -20°C pka -0.01&p
Cas:529-23-7
Min.Order:1 Gram
FOB Price: $66.0
Type:Lab/Research institutions
inquiryHangzhou Huarong Pharm Co., Ltd.established since 2006 , has been actively developing specialty products for Finished Dosages, APIs, Intermediates, and Fine chemicals markets in North America, Europe, Korea, Japan, Mid-East and all over the World. Hu
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Min.Order:1 Kilogram
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Type:Lab/Research institutions
inquiryAppearance:95%+ Package:R&D,Pilot run Transportation:per client require Port:Express ,Air, Sea
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Name: o-aminobenzaldehyde CAS: 529-23-7 State: Gray Solid Content: 99% OLED intermediate Appearance:Gray Solid Storage:keep sealed and keep from direct light Package:According to client's requirements Application:OLED interm
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Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
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Cas:529-23-7
Min.Order:0
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Negotiable
Type:Lab/Research institutions
inquiryConditions | Yield |
---|---|
With formic acid; 2,5-hexanedione for 12h; Autoclave; Inert atmosphere; Green chemistry; | 100% |
With iron; acetic acid In ethanol; water for 0.25h; pH=4.5; | 100% |
With iron; ammonium chloride In ethanol; water for 1 - 4h; Heating / reflux; | 99% |
Conditions | Yield |
---|---|
With hydrotalcite; RuMn2; oxygen In toluene at 60℃; for 21h; atmospheric pressure; | 100% |
With 1,8-diazabicyclo[5.4.0]undec-7-ene; tris(2-methylphenyl)bismuth dichloride In toluene at 20℃; for 0.5h; | 99% |
With 1-methyl-1H-imidazole; [2,2]bipyridinyl; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; tetrakis(acetonitrile)copper(I) trifluoromethanesulfonate In acetonitrile at 20 - 50℃; for 1.75h; Sealed tube; chemoselective reaction; | 99% |
Conditions | Yield |
---|---|
With 2-bromo-2-nitropropane; zinc In methanol at 50℃; for 5h; Yields of byproduct given; | A 98% B n/a |
With potassium hexachloropalatinate(IV); triethanolamine In acetonitrile at 20℃; for 24h; Inert atmosphere; Green light irradiation; | A 71 %Chromat. B 22 %Chromat. |
With platinum on carbon; hydrogen In methanol at 30℃; under 760.051 Torr; for 3h; chemoselective reaction; | A 8 %Spectr. B 20 %Spectr. |
With hydrogen In methanol at 30℃; under 760.051 Torr; for 3h; Catalytic behavior; Solvent; Reagent/catalyst; Temperature; Pressure; chemoselective reaction; | A 91 %Spectr. B 9 %Spectr. |
2-(2'-aminophenyl)-1,3-dithiane
2-aminobenzaldehyde
Conditions | Yield |
---|---|
With ammonium iodide; dihydrogen peroxide; sodium dodecyl-sulfate In water at 20℃; for 0.5h; micellar medium; | 97% |
With 2,4,4,6-Tetrabromo-2,5-cyclohexadien-1-one; dihydrogen peroxide In water; acetonitrile at 20℃; for 1.5h; | 85% |
Conditions | Yield |
---|---|
With 2,3,4,5,7,8,9,10-octahydropyrimido[1,2-a]azepin-1-ium acetate In methanol at 60℃; for 3h; Temperature; Solvent; | 95.9% |
Conditions | Yield |
---|---|
With palladium on activated charcoal; tetrabutylammomium bromide; triethylamine; molybdenum hexacarbonyl In water at 80℃; for 18h; Catalytic behavior; Reagent/catalyst; Sealed tube; | 94% |
With hydrogen iodide; iodine; copper(II) bis(trifluoromethanesulfonate) In dimethyl sulfoxide at 120℃; for 2h; | 30% |
With water; triethylamine In 1,2-dimethoxyethane at 100℃; for 26h; Reagent/catalyst; Sealed tube; Inert atmosphere; | 18% |
With ammonia; iron(II) sulfate | |
at -263.16℃; UV-irradiation; Inert atmosphere; |
2-aminobenzaldehyde
Conditions | Yield |
---|---|
With sodium hydroxide In methanol for 10h; Schlenk technique; Reflux; | 89% |
2-[(1,1,2,2-tetramethyl-1-silapropoxy)methyl]phenylamine
2-aminobenzaldehyde
Conditions | Yield |
---|---|
With zinc dichromate(VI) at 20℃; | 88% |
2-[(trimethylsilyloxy)methyl]benzamine
2-aminobenzaldehyde
Conditions | Yield |
---|---|
With zinc dichromate(VI) at 20℃; | 88% |
2-aminobenzaldehyde
Conditions | Yield |
---|---|
With potassium hydroxide In methanol; water at 80℃; for 16h; | 88% |
2-<2-Amino-benzyloxy>-tetrahydro-pyran
2-aminobenzaldehyde
Conditions | Yield |
---|---|
With zinc dichromate(VI) at 20℃; | 86% |
2-azidobenzaldehyde
2-aminobenzaldehyde
Conditions | Yield |
---|---|
With samarium diiodide In tetrahydrofuran for 0.166667h; Ambient temperature; | 79% |
With hexamethyldisilathiane In methanol for 3h; Ambient temperature; | 78% |
With bis(N,N-diethyldithiocarbamato)dioxomolybdenum(VI); phenylsilane In toluene at 100℃; for 4h; | 70% |
With copper(l) iodide In water; N,N-dimethyl-formamide at 110℃; for 4h; Inert atmosphere; | 45% |
In methyl cyclohexane at -268.96℃; for 0.666667h; Solvent; Temperature; UV-irradiation; Inert atmosphere; |
(2-nitroethenyl)benzene
2-azidobenzaldehyde
A
2-phenyl-3-nitroquinoline
B
2-aminobenzaldehyde
Conditions | Yield |
---|---|
With copper(l) iodide In neat (no solvent) at 110℃; for 8h; Inert atmosphere; | A 75% B 18% |
Conditions | Yield |
---|---|
With dmap; pyridinium chlorochromate In dichloromethane at 0 - 20℃; for 5h; | 71.9% |
Conditions | Yield |
---|---|
Stage #1: anthranilic acid With lithium aluminium tetrahydride In tetrahydrofuran Stage #2: With manganese(IV) oxide In dichloromethane | 67% |
Multi-step reaction with 2 steps 1: lithium aluminium tetrahydride / tetrahydrofuran / 3 h / 20 °C 2: manganese(IV) oxide / dichloromethane / 24 h / 20 °C View Scheme | |
Multi-step reaction with 2 steps 1: lithium aluminium tetrahydride / tetrahydrofuran / 3 h / 20 °C 2: manganese(IV) oxide / dichloromethane / 24 h / 20 °C View Scheme |
Conditions | Yield |
---|---|
With copper(l) iodide; sodium azide; L-proline In dimethyl sulfoxide at 120℃; | 64% |
With copper(l) iodide; sodium azide; N,N,N,N,-tetramethylethylenediamine | 62% |
Conditions | Yield |
---|---|
With water; palladium diacetate; (S)-(1,1'-binaphthalene)-2,2'-diylbis(diphenylphosphine); triethylamine In 1,2-dimethoxyethane at 100℃; for 26h; Sealed tube; Inert atmosphere; | 64% |
methanol
2-nitro-benzaldehyde
A
1-(dimethoxymethyl)-2-nitrobenzene
B
anthranil
C
2-aminobenzaldehyde
Conditions | Yield |
---|---|
With indium; iodine at 50℃; for 2h; Product distribution; Further Variations:; reagents molar ratio, temperature; | A 21% B 55% C 10% |
3-methoxy-3H-1,4-benzodiazepine
2-aminobenzaldehyde
Conditions | Yield |
---|---|
In 1,4-dioxane; water for 20h; Heating; | 54% |
2,3-dimethoxy-2,3-dihydro-1H-benzo[e][1,4]diazepine
2-aminobenzaldehyde
Conditions | Yield |
---|---|
In 1,4-dioxane; water for 15h; Heating; | 52% |
carbon monoxide
2-Nitrobenzyl alcohol
A
2-Aminobenzyl alcohol
B
1,4-dihydro-2H-benzo[d][1,3]oxazin-2-one
C
2-aminobenzaldehyde
Conditions | Yield |
---|---|
With dodecacarbonyl-triangulo-triruthenium; tetraethylammonium chloride In various solvent(s) at 170℃; under 45600 Torr; for 1h; Product distribution; other Pd catalyst; other cocatalyst; var. solvents, reaction time, pressure and temperatures; also substituted benzyl alcohols; | A 22% B 51% C 17% |
2-aminobenzaldehyde
Conditions | Yield |
---|---|
With ammonium hydroxide; copper(ll) sulfate pentahydrate; sodium hydroxide In water at 25℃; for 24h; | 50% |
Conditions | Yield |
---|---|
With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In N,N-dimethyl-formamide at 100℃; for 5h; Catalytic behavior; Schlenk technique; Green chemistry; | A 41% B n/a |
quinazoline
benzoyl chloride
A
N-formylbenzamide
B
N-(2-formylphenyl)benzamide
C
2-aminobenzaldehyde
Conditions | Yield |
---|---|
In chloroform for 0.5h; | A 34% B 33% C 2% |
2-Aminobenzyl alcohol
benzamide
A
2-phenylquinazoline
B
2-aminobenzaldehyde
C
benzoic acid
Conditions | Yield |
---|---|
With cesiumhydroxide monohydrate In 1,4-dioxane at 100℃; for 24h; Schlenk technique; | A 33% B n/a C n/a |
Conditions | Yield |
---|---|
With 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; copper diacetate; silver trifluoromethanesulfonate In 1,2-dichloro-ethane at 110℃; Catalytic behavior; Sealed tube; | A 16% B 24% C 33% |
2-Aminobenzyl alcohol
benzonitrile
A
2-phenylquinazoline
B
2-aminobenzaldehyde
Conditions | Yield |
---|---|
With C39H32Cl2N5PRu; potassium tert-butylate In tert-Amyl alcohol at 130℃; for 0.5h; Sealed tube; | A 28% B 6% |
cyclohexanone
2-nitro-benzaldehyde
A
1,2,3,4-tetrahydroacridine
B
2-aminobenzaldehyde
Conditions | Yield |
---|---|
With chromium dichloride; 4 A molecular sieve; zinc(II) chloride In ethanol at 70℃; | A 23% B n/a |
2-Nitrobenzyl alcohol
sodium ethanolate
A
2-Aminobenzyl alcohol
B
anthranil
C
anthranilic acid
D
2-aminobenzaldehyde
2-aminobenzaldehyde
Conditions | Yield |
---|---|
In ethanol at 20℃; Inert atmosphere; | 100% |
2-aminobenzaldehyde
Conditions | Yield |
---|---|
With methanesulfonic acid In ethanol for 12h; Reflux; Inert atmosphere; | 100% |
2-aminobenzaldehyde
Conditions | Yield |
---|---|
With methanesulfonic acid In ethanol for 12h; Reflux; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
With methanesulfonic acid In ethanol Friedlaender Quinoline Synthesis; Reflux; | 100% |
BARBITURIC ACID
2-aminobenzaldehyde
pyrimido[4,5-b]quinoline-2,4-(1H,3H)-dione
Conditions | Yield |
---|---|
With water at 70℃; for 3h; Friedlaender reaction; | 99% |
With water at 100℃; |
Conditions | Yield |
---|---|
With water at 70℃; for 3h; Friedlaender reaction; | 99% |
With sodium ethanolate In ethanol for 2h; Friedlaender condensation; Heating; | 80% |
With diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate; magnesium triflate In toluene at 35℃; for 36h; Friedlaender Condensation; Molecular sieve; | 41% |
Conditions | Yield |
---|---|
With potassium hydroxide In ethanol for 0.5h; Heating; | 99% |
With potassium hydroxide In ethanol for 36h; Friedlaender Quinoline Synthesis; Reflux; | 97% |
With potassium hydroxide In water at 120℃; for 0.5h; | 96% |
Conditions | Yield |
---|---|
With water at 70℃; for 3h; Friedlaender reaction; | 99% |
With piperidine In ethanol at 100℃; for 24h; Sealed tube; | 57% |
With piperidine In ethanol at 100℃; for 24h; Sealed tube; | 57% |
2-aminobenzaldehyde
chloroacetyl chloride
2-chloro-N-(2-formylphenyl)acetamide
Conditions | Yield |
---|---|
In dichloromethane at 20℃; | 99% |
With pyridine In benzene at 5 - 20℃; for 0.25h; Inert atmosphere; | 56.4% |
Benzoylacetonitrile
2-aminobenzaldehyde
2-phenylquinoline-3-carbonitrile
Conditions | Yield |
---|---|
With water at 70℃; for 3h; Friedlaender reaction; | 99% |
Alkaline conditions; |
Conditions | Yield |
---|---|
With 1,3-dimethylimidazolium sulfate monomethyl ester; L-proline at 90℃; for 0.5h; Knoevenagel Condensation; Green chemistry; | 98% |
With Nafion NR50 In ethanol at 200℃; for 1h; Microwave irradiation; | 95% |
With water at 70℃; for 3h; Friedlaender reaction; | 91% |
2-aminobenzaldehyde
1-methyl-3-phenyl-2-pyrazolin-5-one
1-methyl-3-phenyl-pyrazolo<3,4-b>quinoline
Conditions | Yield |
---|---|
at 150℃; | 98% |
2-aminobenzaldehyde
7,8,9,10-tetrahydroazepino[2,1-b]quinazoline-6,12-dione
Conditions | Yield |
---|---|
With potassium hydroxide In ethanol Friedlaender condensation; Heating; | 98% |
17-isobutyl-3-methoxymorphinan-6-one
2-aminobenzaldehyde
6,7-didehydro-17-isobutyl-3-methoxy-quinolino[2',3':6,7]morphinan
Conditions | Yield |
---|---|
With methanesulfonic acid In ethanol for 20h; Inert atmosphere; Reflux; | 98% |
With methanesulfonic acid In ethanol at 100℃; |
Conditions | Yield |
---|---|
With scandium pentafluorobenzoate In toluene at 20℃; for 12h; | 98% |
2-aminobenzaldehyde
3,4-difluorobenzylamine
Conditions | Yield |
---|---|
With scandium pentafluorobenzoate In toluene at 90℃; for 12h; | 98% |
Conditions | Yield |
---|---|
With potassium tert-butylate In tert-Amyl alcohol at 130℃; for 2h; Reagent/catalyst; Sealed tube; | 98% |
With 1,10-Phenanthroline; iron(II) chloride tetrahydrate; cesiumhydroxide monohydrate In toluene at 130℃; for 24h; Reagent/catalyst; Inert atmosphere; | 95% |
With bromopentacarbonylmanganese(I); N,N,N',N'',N'''-pentamethyldiethylenetriamine; potassium tert-butylate In toluene at 130℃; for 36h; Reagent/catalyst; Sealed tube; Schlenk technique; Inert atmosphere; | 81% |
With cesiumhydroxide monohydrate In 1,4-dioxane at 100℃; for 24h; Schlenk technique; Inert atmosphere; Sealed tube; | 30% |
With potassium tert-butylate In 5,5-dimethyl-1,3-cyclohexadiene at 100℃; for 24h; Inert atmosphere; Schlenk technique; | 16% |
1,3-cylohexanedione
2-aminobenzaldehyde
1-Oxo-1,2,3,4-tetrahydroacridine
Conditions | Yield |
---|---|
With water at 70℃; for 3h; Friedlaender reaction; | 97% |
With tin dioxide for 0.333333h; Heating; Green chemistry; | 90% |
In N,N-dimethyl-formamide 1.) 100 deg C, 30 min, 2.) reflux, 30 min; | 79% |
Conditions | Yield |
---|---|
With potassium hydroxide In methanol; water at 60℃; | 97% |
With potassium hydroxide In ethanol for 12h; Inert atmosphere; Reflux; | 74% |
With potassium hydroxide In ethanol for 2h; Heating; | 36% |
With sodium hydroxide In ethanol Reflux; |
vinyl magnesium bromide
2-aminobenzaldehyde
1-(2'-aminophenyl)prop-2-en-1-ol
Conditions | Yield |
---|---|
In tetrahydrofuran at 60℃; for 2h; | 97% |
In tetrahydrofuran at 20 - 25℃; for 1h; | 59% |
N-tert-butyloxycarbonylpiperidin-4-one
2-aminobenzaldehyde
tert-butyl 3,4-dihydrobenzo[b][1,6]naphthyridine-2(1H)-carboxylate
Conditions | Yield |
---|---|
With 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide In ethyl acetate; N,N-dimethyl-formamide at 90℃; for 0.25h; Friedlaender reaction; Microwave irradiation; | 97% |
Conditions | Yield |
---|---|
With scandium pentafluorobenzoate In toluene at 20℃; for 12h; Reagent/catalyst; Solvent; Temperature; | 97% |
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