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Cas:22047-25-2
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Items Standard Result Assay (Ursolic acid) 98%min 98.22% ----------------------------------------------------------------
Cas:22047-25-2
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top quality 22047-25-2 99%min White powder/large production of Product Name: Acetylpyrazine Synonyms: 1-pyrazinylethanone;1-pyrazinyl-Ethanone;Ethanone, 1-pyrazinyl-;Ethanone,1-pyrazinyl-;K
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Min.Order:1 Kilogram
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inquiryProduct Description Product website: http://www.finerchem.com Product Name Acetylpyrazine CAS No. 22047-25-2 Appearance light yellow crystalline
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Min.Order:1 Gram
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Min.Order:1 Gram
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Min.Order:1 Kilogram
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Min.Order:10 Gram
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inquiry2-Acetylpyrazine CAS: 22047-25-2 Specification Item Standard Test Results Identification A.H-NMR:Comply with the structure Complies B.LC-MS:Comply with the
PRODUCT DETAILS
Cas:22047-25-2
Min.Order:500 Kilogram
FOB Price: $1.0 / 2.0
Type:Lab/Research institutions
inquiryConditions | Yield |
---|---|
With NH4S2O8; silver nitrate; trifluoroacetic acid In dichloromethane; water at 40℃; for 2.5h; | 100% |
With ferrous(II) sulfate heptahydrate; ammonium peroxydisulfate; sulfuric acid In dichloromethane; water at 40℃; Reagent/catalyst; Solvent; Minisci Aromatic Substitution; | 26% |
1-(pyrazin-2-yl)butan-1-one
A
acetylpyrazine
B
2-Methyl-1-pyrazin-2-yl-cyclopropanol
Conditions | Yield |
---|---|
In tert-butyl alcohol; benzene for 4h; Irradiation; | A 1% B 95% |
3-acetylpyrazine N-oxide
acetylpyrazine
Conditions | Yield |
---|---|
With Eosin Y; di-tert-butyl 1,4-dihydro-2,6-dimethyl-3,5-pyridine-dicarboxylate In acetonitrile at 20℃; for 3h; Inert atmosphere; Irradiation; chemoselective reaction; | 90% |
3-methyl-1-(pyrazin-2-yl)butan-1-one
A
acetylpyrazine
B
2,2-dimethyl-1-(pyrazin-2-yl)cyclopropanol
Conditions | Yield |
---|---|
In tert-butyl alcohol; benzene for 4h; Irradiation; | A 2% B 86% |
Conditions | Yield |
---|---|
Stage #1: methylene chloride With iodine; magnesium In tetrahydrofuran at 60℃; for 2h; Inert atmosphere; Stage #2: 2-pyrazine carbonitrile With copper(l) chloride In tetrahydrofuran at 50℃; for 14h; Inert atmosphere; Stage #3: With water In tetrahydrofuran Temperature; Reagent/catalyst; Solvent; Inert atmosphere; | 69% |
acetylpyrazine
Conditions | Yield |
---|---|
With sodium hydrogencarbonate; dimethyl sulfoxide at 80℃; for 6h; | 60% |
1,4-pyrazine
2-oxo-propionic acid
A
acetylpyrazine
B
1,1′-(pyrazine-2,5-diyl)diethanone
Conditions | Yield |
---|---|
With ferrous(II) sulfate heptahydrate; ammonium peroxydisulfate; formic acid; dimethyl sulfoxide In dichloromethane; water at 40℃; Catalytic behavior; Reagent/catalyst; Solvent; Minisci Aromatic Substitution; | A 58% B 10% |
With ferrous(II) sulfate heptahydrate; ammonium peroxydisulfate; sulfuric acid In water at 50℃; Minisci Aromatic Substitution; | A 26% B 33% |
Conditions | Yield |
---|---|
With tert.-butylhydroperoxide; di-tert-butyl peroxide; iron(II) sulfate In dichloromethane; sulfuric acid at 5℃; for 1h; | 50% |
Conditions | Yield |
---|---|
In diethyl ether at 20℃; for 1h; Addition; | 42% |
In diethyl ether at -10 - 10℃; for 1h; | 40% |
Stage #1: 2-pyrazine carbonitrile; methyl magnesium iodide In diethyl ether Stage #2: With water |
2-(3,3-dimethylbutyryl)pyrazine
acetylpyrazine
Conditions | Yield |
---|---|
In hexane for 20h; Irradiation; | 15% |
In tert-butyl alcohol; benzene for 5h; Quantum yield; Irradiation; |
Conditions | Yield |
---|---|
With diethyl ether |
1,4-pyrazine
acetaldehyde
A
acetylpyrazine
B
1,1′-(pyrazine-2,5-diyl)diethanone
Conditions | Yield |
---|---|
With tert.-butylhydroperoxide; sulfuric acid; iron(II) sulfate In water; benzene Yields of byproduct given; | A 28 % Chromat. B n/a |
Conditions | Yield |
---|---|
In dimethyl sulfoxide at 24.9℃; Equilibrium constant; |
pyrazinamide
acetylpyrazine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 85 percent / POCl3 / 1.5 h / 100 °C 2: 40 percent / diethyl ether / 1 h / -10 - 10 °C View Scheme |
2-pyrazine carbonitrile
acetylpyrazine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 2.) H+, H2O 2: 2-methyl-propan-2-ol; benzene / 5 h / Irradiation View Scheme |
L-serin
L-lysine
D-glucose
A
1,4-pyrazine
B
2-Methylpyrazine
C
2,5-dimethyl-pyrazine
D
2,3-dimethylpyrazine
E
acetylpyrazine
F
2-ethyl-3,6-dimethylpyrazine
G
2,6-dimethylpyrazine
H
2,3,5-trimethylpyrazine
I
2-ethyl-6-methylpyrazine
J
2-ethyl-5-methypyrazine
Conditions | Yield |
---|---|
In water at 130℃; for 2h; pH=8; Maillard reaction; |
L-lysine
D-glucose
A
1,4-pyrazine
B
2-Methylpyrazine
C
2,5-dimethyl-pyrazine
D
2,3-dimethylpyrazine
E
acetylpyrazine
F
2-ethyl-3,6-dimethylpyrazine
G
2,6-dimethylpyrazine
H
2,3,5-trimethylpyrazine
I
2-ethyl-3,5-dimethylpyrazine
J
2-ethyl-5-methypyrazine
Conditions | Yield |
---|---|
In water at 130℃; for 2h; pH=8; Maillard reaction; |
2-ethylpyrazine
acetylpyrazine
Conditions | Yield |
---|---|
With tert.-butylhydroperoxide In water at 60℃; for 12h; | 66 %Spectr. |
acetylpyrazine
2-bromo-1-pyrazin-2-yl-ethan-1-one hydrobromide
Conditions | Yield |
---|---|
With pyridinium hydrobromide perbromide; hydrogen bromide In water; acetic acid at 20℃; for 0.1h; | 100% |
With hydrogen bromide; bromine In water at 80 - 90℃; for 1h; | 82% |
With pyridinium hydrobromide perbromide; hydrogen bromide; acetic acid at 20℃; for 1h; | |
With hydrogen bromide; bromine; acetic acid at 23℃; for 4h; Inert atmosphere; |
Conditions | Yield |
---|---|
With acetic acid In ethanol Reflux; | 100% |
acetylpyrazine
Conditions | Yield |
---|---|
With tetrakis(triphenylphosphine) palladium(0) at 120℃; for 72h; | 96% |
Dimethyl oxalate
acetylpyrazine
4-(2-pyrazinyl)-2,4-dioxobutanoic acid methyl ester
Conditions | Yield |
---|---|
Stage #1: acetylpyrazine With lithium hexamethyldisilazane In tetrahydrofuran at -78℃; for 0.75h; Stage #2: Dimethyl oxalate In tetrahydrofuran for 0.166667h; | 96% |
acetylpyrazine
thieno[2,3-d]pyrimidin-4-ylhydrazine
Conditions | Yield |
---|---|
In ethanol for 24h; Reflux; | 96% |
acetylpyrazine
2-(1-hydroxyethyl)pyrazine
Conditions | Yield |
---|---|
Stage #1: acetylpyrazine With C27H43AlClN3Si3; 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane In neat (no solvent) at 20℃; for 16h; Stage #2: With silica gel at 20℃; Catalytic behavior; | 95% |
With sodium tetrahydroborate In methanol Ambient temperature; | |
With lithium aluminium tetrahydride In diethyl ether at -78℃; for 1h; |
Conditions | Yield |
---|---|
With formic acid In ethanol for 4h; Reflux; | 95% |
With formic acid In ethanol for 5h; Reflux; | 90% |
In methanol for 4h; Reflux; | 64% |
Conditions | Yield |
---|---|
dodecacarbonyl-triangulo-triruthenium In toluene at 140℃; for 20h; | 94% |
acetylpyrazine
2-benzyl-3-hydroxy-2,3-dihydro-isoindol-1-one
Conditions | Yield |
---|---|
With Sn(4+)*4C2F6NO4S2(1-)*8C2H6OS In toluene at 110℃; for 24h; Inert atmosphere; Sealed tube; | 94% |
acetylpyrazine
4-bromophenylhydrazine hydrochloride
Conditions | Yield |
---|---|
With sodium acetate In ethanol; chloroform for 12h; Ambient temperature; | 93.5% |
acetylpyrazine
1,3-benzothiazol-2-ylhydrazine
Conditions | Yield |
---|---|
With acetic acid In methanol at 80℃; | 93% |
acetylpyrazine
picolinic acid hydrazide
Conditions | Yield |
---|---|
With formic acid In ethanol for 5h; Reflux; | 93% |
In ethanol |
acetylpyrazine
Conditions | Yield |
---|---|
Stage #1: acetylpyrazine With trimethylaluminum; 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane; 3,3'-bis-(3,5-bis-trifluoromethyl-phenyl)-[1,1']binaphthalenyl-2,2'-diol In toluene at 20℃; for 2h; Glovebox; Inert atmosphere; Stage #2: With methanol for 0.5h; enantioselective reaction; | 93% |
acetylpyrazine
Conditions | Yield |
---|---|
With (R)-xylyl-WALPHOS; triphenylacetic acid; hydrogen; bis(cycloocta-1,5-diene)rhodium(I) trifluoromethanesulfonate In 1,2-dichloro-ethane at 40℃; under 760 Torr; | 92% |
acetylpyrazine
Conditions | Yield |
---|---|
Stage #1: acetylpyrazine With bis(acetylacetonate)nickel(II); (S,S)-2,2'-isopropylidenebis(4-phenyl-2-oxazoline) In isopropyl alcohol at 0℃; for 0.5h; Michael Addition; Schlenk technique; Inert atmosphere; Stage #2: C9H6F3NO2 In isopropyl alcohol at 0℃; for 96h; Michael Addition; Schlenk technique; Inert atmosphere; enantioselective reaction; | 92% |
acetylpyrazine
Conditions | Yield |
---|---|
With C28H29N3O; cobalt(II) aceylacetonate In tert-butyl methyl ether at 20℃; Michael Addition; Schlenk technique; Inert atmosphere; enantioselective reaction; | 92% |
Conditions | Yield |
---|---|
With acetic acid In ethanol Reflux; | 92% |
acetylpyrazine
N,N-dimethyl-formamide dimethyl acetal
3-(N,N-dimethylamino)-1-(pyrazin-2-yl)prop-2-en-1-one
Conditions | Yield |
---|---|
With guanidineacetic acid at 100℃; for 1h; | 91% |
With L-proline In neat (no solvent) at 80℃; for 1.5h; | 90% |
With triethylamine at 110℃; for 16h; | 81% |
acetylpyrazine
trans-1-(4-fluorophenyl)-2-nitro-ethene
(R)-3-(4-fluorophenyl)-4-nitro-1-(pyrazin-2-yl)butan-1-one
Conditions | Yield |
---|---|
With nickel(II) acetate tetrahydrate; (4R,4'R,5S,5'S)-2,2'-(propane-2,2-diyl)bis(4,5-diphenyl-4,5-dihydrooxazole) In isopropyl alcohol at 20℃; for 3h; Michael Addition; Inert atmosphere; enantioselective reaction; | 91% |
2-Aminonicotinaldehyde
acetylpyrazine
2-(pyrazin-2-yl)-1,8-naphthyridine
Conditions | Yield |
---|---|
With potassium hydroxide In methanol; water at 60℃; | 91% |
With potassium hydroxide In methanol at 60℃; Inert atmosphere; Schlenk technique; Reflux; | 85% |
acetylpyrazine
2,5-dihydroxybenzohydrazide
Conditions | Yield |
---|---|
With acetic acid In ethanol for 1h; Reflux; | 91% |
Conditions | Yield |
---|---|
With ammonium acetate In ethanol Reflux; | 91% |
Conditions | Yield |
---|---|
With acetic acid In ethanol Reflux; | 91% |
acetylpyrazine
N,N-dimethyl-formamide dimethyl acetal
3-dimethylamino-1-(3-pyrazinyl)-2-propene-1-one
Conditions | Yield |
---|---|
In 5,5-dimethyl-1,3-cyclohexadiene at 140℃; for 20h; Inert atmosphere; Schlenk technique; | 90.2% |
In xylene Heating; | 73% |
In methanol for 10h; Reflux; | 38% |
for 19h; Heating / reflux; | |
Reflux; |
acetylpyrazine
Conditions | Yield |
---|---|
Stage #1: acetylpyrazine With bis(acetylacetonate)nickel(II); (S,S)-2,2'-isopropylidenebis(4-phenyl-2-oxazoline) In isopropyl alcohol at 0℃; for 0.5h; Michael Addition; Schlenk technique; Inert atmosphere; Stage #2: C10H5F6NO2 In isopropyl alcohol at 0℃; Michael Addition; Schlenk technique; Inert atmosphere; enantioselective reaction; | 90% |
Conditions | Yield |
---|---|
With iodine at 110℃; for 3h; | 88% |
With iodine for 1h; Reflux; | 82% |
With iodine at 90℃; for 1.5h; | 48% |
acetylpyrazine
benzil dihydrazone
Conditions | Yield |
---|---|
for 5h; Heating; | 87% |
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