img _fcksavedurl="/UserAppearance:detailed see specifications Storage:Store in dry, dark and ventilated place. Package:according to the clients requirement Application:108-03-2 Transportation:by air or by sea Port:Shanghai
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Cas:108-03-2
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Cas:108-03-2
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inquiryhigh quality Appearance:White or off white powder Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea Port:shanghai
The above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi
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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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inquiryJ&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia
Massive Chemical is certified with ISO9001 and ISO14001 manufacturer for this product. We will offer all documents as requirement for the materials which includes, Certificate of Analysis, Material Safety Data Sheet, and Method of Analysis and
Zibo Hangyu Biotechnology Development Co., Ltd is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemi
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inquiry1-Nitropropane/108-03-2 /99% purity with low price in stockAppearance:white powder Storage:keep away from heat,sparks and flames Package:according to customers' requirements Application:1-Nitropropane/108-03-2 /99% purity with low price in stock Tran
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Cas:108-03-2
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inquiryhigh purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air Port:Beijing or Guangzhou
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Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
Cas:108-03-2
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1-Nitropropane CAS NO.108-03-2 Application:1-Nitropropane CAS NO.108-03-2
1-Nitropropane CAS NO.108-03-2Appearance:crystal, powder Storage:stay in dry, cool and well-sealed Package:as your request Application:Pharmaceutical intermediates Transportation:By express (Door to door) such as FEDEX, DHL, EMS for small amount. By
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inquiry1-Nitropropane/108-03-2 /99% purity with low price in stockAppearance:white powder Storage:keep away from heat,sparks and flames Package:1 gram/bag Application:1-Nitropropane/108-03-2 /99% purity with low price in stock Transportation:by air or by co
Cas:108-03-2
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Cas:108-03-2
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inquiry1-Nitropropane Basic information Product Name: 1-Nitropropane
Cas:108-03-2
Min.Order:100 Gram
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inquiryLong-term export and transportation experience, 100% processing your order!Fast and safe delivery!Packing: 1kg, 25kg..or base on your inquiy.Our advantages:Long-term export experience allows you to receive goods quickly and safely.1, High quality wit
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Good quality Appearance:Colorless or slightly yellow transparent liquid Package:1MT/IBC drum Application:Used as industrial solvents and pharmaceutical intermediates, explosives, rocket fuel, etc Port:shanghai
United Scientific Company Located in Shanghai of China , is a competitive player in the global specialty and fine chemical market. Fenghua has both the expertise and flexibility to produce a wide range of chemicals. Focusing on developing the innov
Cas:108-03-2
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inquiryConditions | Yield |
---|---|
With magnesium hydroxide; dihydrogen peroxide In propan-1-ol; water at 80℃; under 5250.53 Torr; | 95.5% |
With ammonium hydroxide; dihydrogen peroxide In methanol at 70℃; under 760.051 Torr; Green chemistry; chemoselective reaction; | 97 %Chromat. |
Conditions | Yield |
---|---|
With diethyl ether anschliessend Behandeln mit Wasser; |
Conditions | Yield |
---|---|
at 125 - 130℃; | |
beim Erhitzen; |
Conditions | Yield |
---|---|
With oxygen; nitric acid in der Gasphase; | |
With nitric acid; chlorine in der Gasphase; | |
With bromine; oxygen; nitric acid in der Gasphase; | |
With oxygen; nitric acid; chlorine in der Gasphase; |
Conditions | Yield |
---|---|
With nitric acid at 400℃; | |
With Nitrogen dioxide at 250 - 795℃; | |
With Nitrogen dioxide at 250℃; | |
With nitric acid In water at 285℃; under 72402.6 Torr; Product distribution / selectivity; |
Conditions | Yield |
---|---|
With silver(I) nitrite |
Conditions | Yield |
---|---|
With silver(I) nitrite | |
With poly(N-ethyl-4-vinylpyridinium)nitrite In hexane at 20℃; for 43h; |
Conditions | Yield |
---|---|
With silver(I) nitrite |
Conditions | Yield |
---|---|
With tetrahydrofuran; diethyl ether; Trimethyl borate; sodium at -70℃; |
Conditions | Yield |
---|---|
With nitric acid at 375℃; |
diethyl phosphorylchloridite
aci-1-nitropropane sodium salt
A
(1-nitro-propyl)-phosphonous acid diethyl ester
B
1-Nitropropane
Conditions | Yield |
---|---|
In diethyl ether |
propane
A
i-propyl nitrite
B
n-propyl nitrite
C
isopropyl nitrate
D
propyl nitrate
E
2-nitropropane
F
1-Nitropropane
Conditions | Yield |
---|---|
With dihydrogen peroxide; Nitrogen dioxide at 24.9℃; under 300.02 Torr; Rate constant; Product distribution; Mechanism; boric-acid-coated surface; various pressure and carrier-gas composition; | A 12 % Chromat. B 7 % Chromat. C 16 % Chromat. D 5 % Chromat. E 46 % Chromat. F 14 % Chromat. |
propane
A
i-propyl nitrite
B
isopropyl nitrate
C
propyl nitrate
D
2-nitropropane
E
1-Nitropropane
F
acetone
Conditions | Yield |
---|---|
With dihydrogen peroxide; oxygen; Nitrogen dioxide at 24.9℃; under 300.02 Torr; Rate constant; Product distribution; Mechanism; boric-acid-coated surface; various O2 concn.; |
Cyclopentane
A
formic acid
B
ethene
C
1-nitrobutane
D
1-Nitropropane
E
nitrocyclopentane
Conditions | Yield |
---|---|
With Nitrogen dioxide; sulphur hexafluoride for 0.0166667h; Product distribution; Irradiation; CO2 laser irradiation; products investigated on different reaction conditions; products identified with IR and MS spectra; further cycloalkanes measured; |
Conditions | Yield |
---|---|
With potassium nitrate; sodium nitrite at 150℃; Yield given; | |
With potassium nitrate; sodium nitrite Thermodynamic data; Heating; E; |
1-Nitropropane
Conditions | Yield |
---|---|
With sodium nitrite |
Conditions | Yield |
---|---|
With alkali nitrite | |
With alkaline earth nitrite |
Conditions | Yield |
---|---|
Product distribution; |
Conditions | Yield |
---|---|
Product distribution; |
butyric acid
A
isopropyl nitrate
B
hexane
C
isopropyl butyrate
D
1-Nitropropane
Conditions | Yield |
---|---|
Elektrolyse von Natriumbutyrat; Produkt5: Essigsaeure; Produkt6: Propionsaeure; Produkt7: Glycerin-nitrat(?); und andere Produkten; |
nitric acid
n-butane
A
Nitroethane
B
nitromethane
C
1-nitrobutane
D
1-Nitropropane
Conditions | Yield |
---|---|
at 370 - 450℃; in der Gasphase; |
nitric acid
pentane
A
Nitroethane
B
nitromethane
C
1-nitrobutane
D
1-Nitropropane
Conditions | Yield |
---|---|
at 400℃; bei der Nitrierung enstehen noch: 1-Nitro-pentan,2-Nitro-pentan,3-Nitro-pentan und Aethylen,Propylen und Buten-(1); | |
at 400℃; bei der Nitrierung enstehen noch: 1-Nitro-pentan,2-Nitro-pentan,3-Nitro-pentan; |
tetrahydrofuran
(E)-1-nitroprop-1-ene
diethyl ether
A
2-methyl-1,3-dinitro-pentane
B
1-Nitropropane
Conditions | Yield |
---|---|
at -70℃; |
tetrahydrofuran
(E)-1-nitroprop-1-ene
diethyl ether
A
2-methyl-1,3-dinitro-pentane
B
1-Nitropropane
Conditions | Yield |
---|---|
at -70℃; |
Dipropyl ether
nitric acid
A
Nitroethane
B
nitromethane
C
1-Nitropropane
Conditions | Yield |
---|---|
at 400℃; |
propionaldehyde oxime
A
propionohydroxamic acid
B
1-Nitropropane
propane
nitric acid
A
Nitroethane
B
nitromethane
C
2-nitropropane
D
1-Nitropropane
Conditions | Yield |
---|---|
at 250 - 795℃; in der Gasphase meist bei ca.400grad; weitere Produkte: Aethylen und Propylen; | |
at 250 - 795℃; in der Gasphase meist bei ca.400grad; | |
at 250 - 795℃; in der Gasphase meist bei ca.400grad; weitere Produkte: Propylalkohol und Isopropylalkohol; | |
at 410℃; under 5884.06 - 8826.09 Torr; |
propane
A
Nitroethane
B
nitromethane
C
2-nitropropane
D
1-Nitropropane
Conditions | Yield |
---|---|
at 250 - 795℃; in der Gasphase meist bei ca.400grad; | |
at 250 - 795℃; in der Gasphase meist bei ca.400grad; weitere Produkte: Aethylen und Propylen; | |
at 250 - 795℃; in der Gasphase meist bei ca.400grad; weitere Produkte: Propylalkohol und Isopropylalkohol; |
dibutyl ether
nitric acid
A
Nitroethane
B
nitromethane
C
1-nitrobutane
D
1-Nitropropane
Conditions | Yield |
---|---|
at 400℃; durch ein Glasrohr;Produkt 5:Butyl-nitrobutyl-aether; |
Conditions | Yield |
---|---|
With P(i-PrNCH2CH2)3N; magnesium sulfate for 1.25h; Ambient temperature; | 99% |
With tetrabutyl ammonium fluoride; tert-butyldimethylsilyl chloride; triethylamine In tetrahydrofuran for 0.0833333h; | 92% |
With Amberlyst A-21 for 10h; | 84% |
Yield given. Multistep reaction; | |
With potassium hydrogencarbonate |
1-Nitropropane
4-methylbenzaldehyde N-(tert-butoxycarbonyl)imine
tert-butyl (1R,2S)-2-nitro-1-p-tolylpropylcarbamate
Conditions | Yield |
---|---|
With N-((1R,2R)-2-(3-((1R,2R)-2-(dimethylamino)cyclohexyl)thioureido)-1,2-diphenylethyl)-3,5-bis(trifluoromethyl)benzenesulfonamide In acetonitrile at -20℃; Mannich reaction; Molecular sieve; | 99% |
Conditions | Yield |
---|---|
Stage #1: 1-Nitropropane With C19H20F2N2O4; Nd5O(OiPr)13; water; sodium hexamethyldisilazane In tetrahydrofuran at 0 - 20℃; Inert atmosphere; Stage #2: benzaldehyde In tetrahydrofuran at -40℃; for 20h; Inert atmosphere; optical yield given as %ee; diastereoselective reaction; | 99% |
methyl o-formylbenzoate
1-Nitropropane
3-(1-nitropropyl)-1(3H)-isobenzofuranone
Conditions | Yield |
---|---|
With potassium carbonate at 20℃; for 8h; Neat (no solvent); | 99% |
1-Nitropropane
tert-butyl N-(phenyl(phenylsulfonyl)methyl)carbamate
Conditions | Yield |
---|---|
With (S)-N-benzyl-2-(3-((S)-1-hydroxy-3-phenylpropan-2-yl)ureido)-N,N,3,3-tetramethylbutan-1-aminium bromide; potassium hydroxide In chloroform at -20℃; for 12h; Mannich Aminomethylation; stereoselective reaction; | 99% |
With C36H41N4O3(1+)*Br(1-); potassium hydroxide In chloroform at -20℃; for 12h; Mannich Aminomethylation; stereoselective reaction; | 95% |
Conditions | Yield |
---|---|
With hydrogen In ethanol at 109.84℃; under 18751.9 Torr; for 7.5h; Autoclave; Green chemistry; chemoselective reaction; | 99% |
3-nitro-benzaldehyde
1-Nitropropane
2-nitro-1-(3-nitro-phenyl)-butan-1-ol
Conditions | Yield |
---|---|
With N-benzyl-trimethylammonium hydroxide In tetrahydrofuran; water at 20℃; for 0.1h; | 98% |
With diethyl ether; sodium methylate | |
With triethylamine |
3-ethoxy-2-methyl-but-3-en-2-ol
1-Nitropropane
2-(5-Ethoxy-3-ethyl-4,5-dihydro-isoxazol-5-yl)-propan-2-ol
Conditions | Yield |
---|---|
With phenyl isocyanate; triethylamine In benzene | 98% |
1-methyl-3,6,8-trinitro-2-quinolone
1-Nitropropane
6,8-dinitro-1-methyl-4(1-nitropropyl)-2-quinolone
Conditions | Yield |
---|---|
With triethylamine In acetonitrile at 80℃; for 3h; regioselective reaction; | 98% |
N-(p-chlorobenzylidene)-p-toluenesulfonamide
1-Nitropropane
C17H19ClN2O4S
Conditions | Yield |
---|---|
With nanocrystalline magnesium oxide In N,N-dimethyl-formamide at 20℃; for 0.25h; aza-Henry reaction; | 98% |
1-Nitropropane
Conditions | Yield |
---|---|
With 1,8-diazabicyclo[5.4.0]undec-7-ene In toluene Aza-Henry Reaction; | 98% |
Conditions | Yield |
---|---|
With hydrogen at 100℃; under 7500.75 Torr; for 12h; Sealed tube; Autoclave; | 97% |
With sodium tetrahydroborate; nickel(II) chloride hexahydrate In water at 20℃; for 3h; Inert atmosphere; Green chemistry; | 96% |
Stage #1: 1-Nitropropane In water at 20℃; for 0.0166667h; Stage #2: With sodium tetrahydroborate In water at 50℃; for 0.133333h; | 95% |
Conditions | Yield |
---|---|
With P(i-PrNCH2CH2)3N; magnesium sulfate for 2.25h; Ambient temperature; | 97% |
With P(i-BuNCH2CH2)3N; magnesium sulfate at 25℃; for 2h; Henry reaction; | 96% |
With tetrabutyl ammonium fluoride; tert-butyldimethylsilyl chloride; triethylamine In tetrahydrofuran for 0.0833333h; | 90% |
Conditions | Yield |
---|---|
With aluminum oxide; potassium fluoride In tetrahydrofuran for 2h; | 97% |
ethyl 2-(2-oxoindolin-3-ylidene)cyanoacetate
1-Nitropropane
Conditions | Yield |
---|---|
With C26H36N4OS at -10℃; for 3h; Michael condensation; Neat (no solvent); optical yield given as %ee; enantioselective reaction; | A 97% B n/a |
Conditions | Yield |
---|---|
With 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; oxygen at 60℃; under 760.051 Torr; for 27h; | 97% |
Conditions | Yield |
---|---|
With sodium azide; ammonium acetate; acetic acid In N,N-dimethyl-formamide at 100℃; | 97% |
Stage #1: benzaldehyde With sodium azide; sodium hydrogen sulphite; sodium sulfite In dimethyl sulfoxide at 110℃; Inert atmosphere; Stage #2: 1-Nitropropane In dimethyl sulfoxide Inert atmosphere; | 50% |
1-Nitropropane
Conditions | Yield |
---|---|
With lithium methanolate In ethanol at 0 - 20℃; Inert atmosphere; | 97% |
2-hydrazinoquinoline
1-Nitropropane
1-ethyl-[1,2,4]triazolo[4,3-a]quinoline
Conditions | Yield |
---|---|
Stage #1: 1-Nitropropane With polyphosphoric acid at 130℃; Stage #2: 2-hydrazinoquinoline at 130℃; | 97% |
methyl crotonate
1-Nitropropane
methyl 3-methyl-4-nitrohexanoate
Conditions | Yield |
---|---|
With tetrabutyl ammonium fluoride In tetrahydrofuran at 30℃; under 10000 Torr; for 120h; | 96% |
With triethylamine In dichloromethane under 11250900 Torr; for 48h; Ambient temperature; | 95% |
Conditions | Yield |
---|---|
With aluminum oxide; potassium fluoride In tetrahydrofuran for 2h; | 96% |
With 1,8-diazabicyclo[5.4.0]undec-7-ene In acetonitrile Ambient temperature; | 77% |
With sodium methylate In methanol Heating; | 46% |
4-nitrobenzaldehdye
1-Nitropropane
2-nitro-1-(4-nitrophenyl)butan-1-ol
Conditions | Yield |
---|---|
With polymer supported 4-DMAP at 20℃; for 0.5h; Henry Nitro Aldol Condensation; | 96% |
With Streptorerticillium griseoverticillatum protein-glutamine γ-glutamyltransferase In dichloromethane; water at 30℃; for 72h; Henry reaction; Enzymatic reaction; optical yield given as %de; | 94% |
With polystyryl-diphenylphosphine-ethyl acrylate complex In neat (no solvent) at 20℃; for 3h; Henry Nitro Aldol Condensation; Green chemistry; | 94% |
dimethyl (Z)-2-(bromomethyl)fumarate
1-Nitropropane
(E)-1-ethyl-2,3-dimethoxycarbonyl buta-1,3-diene
Conditions | Yield |
---|---|
With sodium hydroxide In tetrahydrofuran at 20℃; for 4h; | 96% |
With sodium hydroxide In tetrahydrofuran at 20℃; for 2h; | 96% |
Conditions | Yield |
---|---|
With nanocrystalline magnesium oxide In N,N-dimethyl-formamide at 20℃; for 0.25h; aza-Henry reaction; | 96% |
Conditions | Yield |
---|---|
With copper(I) trifluoromethanesolfonate toluene complex; (+)-6,6'-(((1R,2R,4R,5R)-bicyclo[2.2.2]octane-2,5-diylbis(azanediyl))bis(methylene))bis(2,4-di-tert-butylphenol) In methanol at 40℃; for 24h; Henry Nitro Aldol Condensation; Molecular sieve; enantioselective reaction; | 96% |
methyl 2-oxo-2-phenylacetate
1-Nitropropane
Conditions | Yield |
---|---|
With tetrahydrofuran; 2-methyltetrahydrofuran; Nitroethane; neodymium(III) chloride hexahydrate; (S)-2-fluoro-N-(1-((4-fluoro-2-hydroxyphenyl)amino)-3,3-dimethyl-1-oxobutan-2-yl)-5-hydroxybenzamide; sodium t-butanolate at -78℃; for 48h; Kinetics; Reagent/catalyst; Aldol Addition; Inert atmosphere; stereoselective reaction; | 96% |
1-Nitropropane
propionic acid
Conditions | Yield |
---|---|
With acetic acid; zinc(II) iodide In toluene at 110℃; for 24h; Catalytic behavior; Reagent/catalyst; Solvent; | 95% |
With sulfuric acid | |
With water; benzenesulfonic acid |
Conditions | Yield |
---|---|
In aq. phosphate buffer at 20℃; for 72h; pH=7.0; Henry Nitro Aldol Condensation; Overall yield = 70%; Overall yield = 36.6 mg; diastereoselective reaction; | A n/a B 95% |
With n-butyllithium; acetic acid THF-DMPU-hexane, 1.) a.) -88 to -60 deg C, 75 min; b.) -70 to -60 deg C, 1.5 h; 2.) -90 to -85 deg C; Yield given. Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts; |
4-nitrobenzaldehdye
1-Nitropropane
2-nitro-1-(4-nitrophenyl)butan-1-ol
2-nitro-1-(4-nitrophenyl)butan-1-ol
Conditions | Yield |
---|---|
In aq. phosphate buffer at 20℃; for 50h; pH=7.0; Henry Nitro Aldol Condensation; Overall yield = 87%; Overall yield = 52.2 mg; diastereoselective reaction; | A n/a B 95% |
Product distribution; var. ratio of educts, var. nitroalkanes, var. aldehydes; | A 60% B n/a |
Yield given. Multistep reaction. Yields of byproduct given; |
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