3-(2-phenylethenyl)pyridazine
pyridazine-3 carboxaldehyde
Conditions | Yield |
---|---|
With sodium periodate; osmium(VIII) oxide In water; acetone; tert-butyl alcohol at 20℃; for 48h; | 81% |
3-hydroxymethylpyridazine
pyridazine-3 carboxaldehyde
Conditions | Yield |
---|---|
With selenium(IV) oxide In 1,4-dioxane for 2h; Heating; | 52% |
With manganese(IV) oxide In 1,2-dichloro-ethane at 70℃; for 4h; |
Conditions | Yield |
---|---|
In methanol Heating; | 95% |
pyridazine-3 carboxaldehyde
4-(2-pyridylmethyl)thiosemicarbazide
C12H12N6S
Conditions | Yield |
---|---|
In methanol Heating; | 94% |
pyridazine-3 carboxaldehyde
pyridazine-3-carbaldehyde oxime
Conditions | Yield |
---|---|
With hydroxylamine hydrochloride; potassium carbonate In ethanol; water standing overnight in refrigerator; | 89% |
With hydroxylamine hydrochloride; potassium carbonate In ethanol at 80℃; for 2h; | 52% |
(E)-(2-nitrovinyl)cyclohexane
pyridazine-3 carboxaldehyde
(S)-2-cyclohexyl-3-nitro-1-(pyridazin-3-yl)propan-1-one
Conditions | Yield |
---|---|
With (5R,7R)-7-fluoro-5-isopropyl-2-(perfluorophenyl)-6,7-dihydro-5H-pyrrolo[2,1c][1,2,4]triazol-2-ium tetrafluoroborate; N-ethyl-N,N-diisopropylamine In methanol at 0℃; Stetter reaction; Inert atmosphere; optical yield given as %ee; enantioselective reaction; | 88% |
(E)-methyl 3-cyanoacrylate
pyridazine-3 carboxaldehyde
Methyl 3-(3-Pyridazinyl)-2-cyanoacrylate
Conditions | Yield |
---|---|
triethylamine In methanol 50-60 deg C, 30 seconds, then r.t., 2h; | 87% |
azepane-1-carbothioic acid hydrazide
pyridazine-3 carboxaldehyde
Conditions | Yield |
---|---|
With acetic acid In methanol for 2h; Heating; | 86% |
pyrrolidine-1-carbothioic acid hydrazide
pyridazine-3 carboxaldehyde
Conditions | Yield |
---|---|
With acetic acid In methanol for 2h; Heating; | 86% |
piperidine-1-carbothioic acid hydrazide
pyridazine-3 carboxaldehyde
Conditions | Yield |
---|---|
With acetic acid In methanol for 2h; Heating; | 85% |
hydrazinecarbodithioic acid methyl ester
pyridazine-3 carboxaldehyde
Conditions | Yield |
---|---|
In isopropyl alcohol at 65 - 70℃; for 1h; | 85% |
pyridazine-3 carboxaldehyde
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; for 1h; | 79% |
Conditions | Yield |
---|---|
In methanol Heating; | 74% |
(S)-{cyclopropyl[4-(difluoromethoxy)phenyl]methyl}amine
pyridazine-3 carboxaldehyde
[(R)-cyclopropyl-(4-difluoromethoxyphenyl)methyl]pyridazin-3-ylmethylarnine
Conditions | Yield |
---|---|
Stage #1: (S)-{cyclopropyl[4-(difluoromethoxy)phenyl]methyl}amine; pyridazine-3 carboxaldehyde With sodium tris(acetoxy)borohydride; acetic acid In 1,2-dichloro-ethane at 20 - 35℃; Inert atmosphere; Stage #2: With potassium carbonate In water; 1,2-dichloro-ethane | 73% |
3-azabicyclo<3.2.2>nonane-3-thiocarboxylic acid hydrazide
pyridazine-3 carboxaldehyde
Conditions | Yield |
---|---|
With acetic acid In methanol for 2h; Heating; | 72% |
pyridazine-3 carboxaldehyde
(6-chloropyridin-3-yl)(pyridazin-3-yl)methanone
Conditions | Yield |
---|---|
With 2-pentafluorophenyl-6,7-dihydro-5H-pyrrolo[2,1-c][1,2,4]triazol-2-ium tetrafluoroborate; dmap; water In dichloromethane at -40℃; for 16h; Inert atmosphere; | 63% |
1H-indene-1,3(2H)-dione
pyridazine-3 carboxaldehyde
Conditions | Yield |
---|---|
With piperidine In methanol for 1.5h; Heating; | 62% |
Conditions | Yield |
---|---|
In methanol Heating; | 60% |
pyridazine-3 carboxaldehyde
(triphenylphosphoranylidene)acetaldehyde
3-(3-Pirydazinyl)-propenal
Conditions | Yield |
---|---|
In benzene at 5℃; for 2h; | 59% |
Methyl diethylphosphonoacetate
pyridazine-3 carboxaldehyde
Conditions | Yield |
---|---|
Stage #1: Methyl diethylphosphonoacetate With sodium hydride In tetrahydrofuran; mineral oil at 0℃; for 0.5h; Inert atmosphere; Stage #2: pyridazine-3 carboxaldehyde In tetrahydrofuran; mineral oil at 0℃; for 1.5h; | 57% |
diethoxyphosphoryl-acetic acid ethyl ester
pyridazine-3 carboxaldehyde
ethyl (E)-3-(pyridazin-3-yl)acrylate
Conditions | Yield |
---|---|
Stage #1: diethoxyphosphoryl-acetic acid ethyl ester With sodium hydride In tetrahydrofuran; mineral oil at 0℃; for 0.5h; Stage #2: pyridazine-3 carboxaldehyde In tetrahydrofuran; mineral oil at 0 - 20℃; for 1h; | 50.97% |
Stage #1: diethoxyphosphoryl-acetic acid ethyl ester With sodium hydride In tetrahydrofuran; mineral oil at 0℃; for 0.5h; Stage #2: pyridazine-3 carboxaldehyde In tetrahydrofuran; mineral oil at 20℃; for 1h; | 50.97% |
With sodium hydride; N,N-dimethyl-formamide at 60℃; for 4h; | 44% |
acetoacetic acid methyl ester
pyridazine-3 carboxaldehyde
Dimethyl 2,6-Dimethyl-4-(3-pyridazinyl)-1,4-dihydropyridine-3,5-dicarboxylate
Conditions | Yield |
---|---|
With ammonium hydroxide In methanol for 1h; Heating; | 49% |
pyridazine-3 carboxaldehyde
malonic acid dimethyl ester
Dimethyl malonate
Conditions | Yield |
---|---|
diethylamine In methanol at -10℃; for 5h; | 45% |
1-(2-hydroxyethyl)piperazine
2-thioxo-4-thiazolidinone
pyridazine-3 carboxaldehyde
Conditions | Yield |
---|---|
With acetic acid In methanol for 4h; Reflux; Inert atmosphere; | 37.1% |
pyridazine-3 carboxaldehyde
malonic acid dimethyl ester
Dimethyl (3-Pyridazinylmethylene)malonate
Conditions | Yield |
---|---|
diethylamine In dichloromethane for 10h; Ambient temperature; | 30% |
isopropyl acetoacetate
pyridazine-3 carboxaldehyde
Diisopropyl 2,6-Dimethyl-4-(3-pyridazinyl)-1,4-dihydropyridine-3,5-dicarboxylate
Conditions | Yield |
---|---|
With ammonium hydroxide In methanol for 12h; Heating; | 28% |
malonic acid
pyridazine-3 carboxaldehyde
(E)-3-(pyridazin-3-yl)acrylic acid
Conditions | Yield |
---|---|
With pyridine at 80℃; for 2h; | 27% |
pyridazine-3 carboxaldehyde
Conditions | Yield |
---|---|
Stage #1: C11H10F3IN2O5S; pyridazine-3 carboxaldehyde With 2-pentafluorophenyl-6,7-dihydro-5H-pyrrolo[2,1-c][1,2,4]triazol-2-ium tetrafluoroborate; tert-butyl alcohol In 1,2-dichloro-ethane at 0℃; for 0.0833333h; Schlenk technique; Sealed tube; Inert atmosphere; Stage #2: With N,N,N,N,-tetramethylethylenediamine In 1,2-dichloro-ethane at 0℃; for 10h; Schlenk technique; Sealed tube; Inert atmosphere; | 26% |
ethyl acetoacetate
pyridazine-3 carboxaldehyde
Diethyl 2,6-Dimethyl-4-(3-pyridazinyl)-1,4-dihydropyridine-3,5-dicarboxylate
Conditions | Yield |
---|---|
With ammonium hydroxide In methanol for 1h; Heating; | 22% |
ethyl aminocrotonate
acetoacetic acid methyl ester
pyridazine-3 carboxaldehyde
Ethyl Methyl 2,6-Dimethyl-4-(3-pyridazinyl)-1,4-dihydropyridine-3,5-dicarboxylate
Conditions | Yield |
---|---|
1) EtOH, reflux, 10 min, 2) EtOH, reflux, 2.5h; Yield given. Multistep reaction; |
Molecule structure of Pyridazine-3-carbaldehyde (CAS NO.60170-83-4):
Molecular Weight: 108.0981 g/mol
Molecular Formula: C5H4N2O
Density: 1.235 g/cm3
Boiling Point: 300.361 °C at 760 mmHg
Flash Point: 139.901 °C
Index of Refraction: 1.581
Molar Refractivity: 29.188 cm3
Molar Volume: 87.547 cm3
Surface Tension: 57.072 dyne/cm
Enthalpy of Vaporization: 54.042 kJ/mol
Vapour Pressure: 0.001 mmHg at 25 °C
InChI: InChI=1/C5H4N2O/c8-4-5-2-1-3-6-7-5/h1-4H
InChIKey: YRUFRSUZZACWCW-UHFFFAOYAW
Product Categories of Pyridazine-3-carbaldehyde (CAS NO.60170-83-4): ALDEHYDE
Pyridazine-3-carbaldehyde (CAS NO.60170-83-4) is also named as 3-pyridazinecarboxaldehyde ; 3-Pyridazinecarbaldehyde, 97% ; 3-Pyridazinecarboxaldehyde (6CI, 9CI) .
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