CAS No.627-05-4,1-NITROBUTANE Suppliers,MSDS download

Dayang Chem (Hangzhou) Co.,Ltd.

As a leading manufacturer and supplier of chemicals in China, DayangChem not only supply popular chemicals, but also DayangChem's R&D center offer custom synthesis services. DayangChem can provide different quantities of custom synthesis ch

1-Nitrobutane

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Chemwill Asia Co., Ltd.

Our main production base is located in Xuzhou industry park. We are certified both to the ISO 9001 and ISO 14001 Standards, have a safety management system in place.Our R&D team masters core technology for process-design of target building block

1-Nitrobutane

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Zibo Hangyu Biotechnology Development Co., Ltd

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

High Purity 1-nitrobutane

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Zhuozhou Wenxi import and Export Co., Ltd

Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard

factory directly supply CAS 627-05-4 with competitive price

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Antimex Chemical Limied

Ansciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali

Butane, 1-nitro-

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Henan Tianfu Chemical Co., Ltd.

Butane, 1-nitro- Application:Organic Chemicals

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Changzhou Extraordinary Pharmatech co.,LTD

Changzhou Extraordinary Pharmatech co., LTD. As a leading chemical manufacturer and supplier in China.DAS authentication is passed.We can provide the popular precursor chemicals, we have our own strong R & D team, have our own laboratories and fa

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Shanghai united Scientific Co.,Ltd.

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 innovat

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Nanjing Raymon Biotech Co., Ltd.

1-nitrobutane Storage:Store in dry and cool condition Package:25kg or according to cutomer's demand Application:Chemical research/Pharmaceutical intermediates Transportation:By Sea,by Air,By courier like DHL or Fedx. Port:Shanghai/Shenzhen

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Hebei Ruishun Trade Co.,Ltd

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Debye Scientific

Debyesci is here who supplied several kinds of chemical products to global pharmaceutical, drug discovery, agrochemical and biotechnology industries for four yearsOur key scientific leadership team has gained experience in top research and developmen

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Changzhou Foreign Trade Corp

CFTC?PharmaChem?is?a?service?based?company?in?China,?a?pharmachem?division?of?Changzhou?Foreign?Trade?Corp.,supplying?raw?materials,?intermediates,?APIs?and?fine?chemicals?for?the?pharmaceutical?and?specialty?chemical?industries?worldwide. Applicatio

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Chemical Co.Ltd

Manufacturer,strong R&D,professional team Storage:Store in a cool, dry place. Store in a tightly closed container. Package:according to your requirement Application:ZhiShang Chemical is owned by ZhiShang Group, is a professional new-type chemicals en

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NovaChemistry

high purity Application:Drug intermediates Materials intermediates and active molecules

1-nitrobutane

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Sigma-Aldrich Chemie GmbH

Low-energy velocity map photoelectron imaging of 1-nitrobutane anions by photoelectron spectroscopy has been reported. Hydrothermal reaction of 1-nitrobutane in high-temperature water has been reported. Package:5 g in glass bottle

1-Nitrobutane

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Synthetic route

: 109-65-9
1-bromo-butane

: 627-05-4
1-nitrobutane

Conditions

Conditions	Yield
With poly(vinylbenzyltriphenylphosphonium nitrite) In toluene at 100℃; for 8h;	98%
With poly(N-butyl-4-vinylpyridinium)nitrite In hexane at 20℃; for 72h;	90%
With poly(vinylbenzyltriphenylphosphonium)*NO2(-) In benzene for 24h; Ambient temperature;	21%
With silver(I) nitrite In dimethyl sulfoxide

: 110-69-0
butyraldehyde oxime

: 627-05-4
1-nitrobutane

Conditions

Conditions	Yield
With triethanolamine; dihydrogen peroxide In water; acetonitrile at 85℃; under 4650.47 Torr;	95.8%
With ammonium hydroxide; dihydrogen peroxide In methanol at 70℃; under 760.051 Torr; Green chemistry; chemoselective reaction;	96 %Chromat.

: 14850-23-8
trans-4-Octene

A: 627-05-4
1-nitrobutane

B: 107-92-6
butyric acid

Conditions

Conditions	Yield
	A 90% B n/a

: 109-73-9
N-butylamine

: 627-05-4
1-nitrobutane

Conditions

Conditions	Yield
With tert.-butylhydroperoxide; chromium silicalite-2 In methanol at 65℃; for 5h;	80%
With tert.-butylhydroperoxide; molecular sieve In methanol for 5h; Heating;	80%
With 3,3-dimethyldioxirane In acetone for 0.5h; Ambient temperature;	84 % Chromat.

: 693-04-9
butyl magnesium bromide

: 627-05-4
1-nitrobutane

Conditions

Conditions	Yield
With dinitrogen tetraoxide In tetrahydrofuran -190 deg C -> room temperature;	71%

: 27675-37-2, 3156-71-6
1-nitrobut-1-ene

: 627-05-4
1-nitrobutane

Conditions

Conditions	Yield
With sodium tetrahydroborate; silica gel In i-Amyl alcohol; chloroform at 20℃; for 2h; Inert atmosphere;	59%

: 109-72-8, 29786-93-4
n-butyllithium

: 627-05-4
1-nitrobutane

Conditions

Conditions	Yield
With dinitrogen tetraoxide In tetrahydrofuran -190 deg C -> room temperature;	19%

: 109-65-9
1-bromo-butane

A: 544-16-1
n-Butyl nitrite

B: 627-05-4
1-nitrobutane

Conditions

Conditions	Yield
With tetraphenylphosphonium nitrite (ionic form) Yield given. Yields of byproduct given;
With silver(I) nitrite; diethyl ether
With silver(I) nitrite; Petroleum ether
With tetraphenylphosphonium nitrite (ionic form) Yield given. Yields of byproduct given;

: 3638-64-0
1-nitroethylene

: 925-90-6
ethylmagnesium bromide

: 627-05-4
1-nitrobutane

Conditions

Conditions	Yield
With diethyl ether

: 542-69-8
1-iodo-butane

A: 544-16-1
n-Butyl nitrite

B: 627-05-4
1-nitrobutane

Conditions

Conditions	Yield
With tetraphenylphosphonium nitrite (ionic form) Yield given. Yields of byproduct given;
With silver(I) nitrite; Petroleum ether
With silver(I) nitrite; diethyl ether
With tetraphenylphosphonium nitrite (ionic form) Yield given. Yields of byproduct given;

: 563-17-7
potassium ethyl sulfate

: 627-05-4
1-nitrobutane

Conditions

Conditions	Yield
With potassium nitrite
With sodium nitrite

: 106-97-8
n-butane

A: 600-24-8, 116783-22-3
2-nitrobutane

B: 627-05-4
1-nitrobutane

Conditions

Conditions	Yield
With nitric acid at 420℃;
With nitric acid In water at 200℃; under 77574.3 Torr; for 0.0333333h; Product distribution / selectivity;

: 106-97-8
n-butane

: 627-05-4
1-nitrobutane

Conditions

Conditions	Yield
With nitric acid at 400 - 440℃;

: 110-69-0
butyraldehyde oxime

A: 109-74-0
propyl cyanide

B: 627-05-4
1-nitrobutane

Conditions

Conditions	Yield
With potassium phosphate; D-glucose 6-phosphate; phenobarbital-induced rat liver microsomes; potassium chloride; nicotinamide adenine dinucleotide phosphate; magnesium chloride; glucose 6-phosphate dehydrogenase Mechanism; multistep reaction; dehydration of n-butyraldoxime catalyzed by cytochrome P-450;

: 109-69-3
n-Butyl chloride

: 627-05-4
1-nitrobutane

Conditions

Conditions	Yield
With perhydrodibenzo-18-crown-6; potassium nitrite at 70℃; for 5h; Yield given;

: 287-92-3
Cyclopentane

A: 64-18-6
formic acid

B: 74-85-1
ethene

C: 627-05-4
1-nitrobutane

D: 108-03-2
1-Nitropropane

E: 2562-38-1
nitrocyclopentane

Conditions

Conditions	Yield
With Nitrogen dioxide; sulfur(VI) 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;

...Expand

: 106-97-8
n-butane

A: 544-16-1
n-Butyl nitrite

B: 928-45-0
butyl nitrate

C: 924-43-6
sec-butyl nitrite

D: 600-24-8, 116783-22-3
2-nitrobutane

E: 924-52-7
2-butyl nitrate

F: 627-05-4
1-nitrobutane

Conditions

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 6 % Chromat. B 0.3 % Chromat. C 31 % Chromat. D 51 % Chromat. E 3 % Chromat. F 7 % Chromat.

...Expand

: 109-73-9
N-butylamine

A: 3378-31-2, 26049-02-5
(E)-1,2-dibutyldiazene 1,2-dioxide

B: 44426-95-1
n-Butylnitrit

C: 627-05-4
1-nitrobutane

Conditions

Conditions	Yield
With oxaziridinium tetrafluoroborate derived from N-methyl-1,2,3,4-tetrahydroisoquinoline In dichloromethane at 20℃; for 48h; Yields of byproduct given;	A n/a B n/a C 15 % Spectr.

...Expand

: 1000-67-5
sodium butylsulfate

: 627-05-4
1-nitrobutane

Conditions

Conditions	Yield
With potassium nitrate; sodium nitrite at 190℃; Yield given;
With potassium nitrate; sodium nitrite Thermodynamic data; Heating; E;

: 109-65-9
1-bromo-butane

silver nitrite: silver nitrite

A: 544-16-1
n-Butyl nitrite

B: 627-05-4
1-nitrobutane

...Expand

: 542-69-8
1-iodo-butane

silver nitrite: silver nitrite

A: 544-16-1
n-Butyl nitrite

B: 627-05-4
1-nitrobutane

...Expand

: 7697-37-2
nitric acid

: 106-97-8
n-butane

A: 79-24-3
Nitroethane

B: 75-52-5
nitromethane

C: 600-24-8, 116783-22-3
2-nitrobutane

D: 627-05-4
1-nitrobutane

Conditions

Conditions	Yield
at 420℃; Produkt ist noch:1-Nitro-propan;
at 420℃; Produkte sind noch: 1-Nitro-propan, Aethylen, Propylen, Buten-(1) und Buten-(2);
at 420℃; Produkt ist noch:1-Nitro-propan;

...Expand

: 7697-37-2
nitric acid

: 106-97-8
n-butane

A: 79-24-3
Nitroethane

B: 75-52-5
nitromethane

C: 627-05-4
1-nitrobutane

D: 108-03-2
1-Nitropropane

Conditions

Conditions	Yield
at 370 - 450℃; in der Gasphase;

...Expand

: 7697-37-2
nitric acid

: 109-66-0
pentane

A: 79-24-3
Nitroethane

B: 75-52-5
nitromethane

C: 627-05-4
1-nitrobutane

D: 108-03-2
1-Nitropropane

Conditions

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;

...Expand

: 3638-64-0
1-nitroethylene

: 60-29-7
diethyl ether

: 925-90-6
ethylmagnesium bromide

A: 627-05-4
1-nitrobutane

B hexanone-(3)-oxime: hexanone-(3)-oxime

Conditions

Conditions	Yield
at 10 - 15℃; und bei folgendem Kochen;

...Expand

standardbutyl iodide: standardbutyl iodide

: 627-05-4
1-nitrobutane

Conditions

Conditions	Yield
With silver(I) nitrite

: 540-82-9
ethyl sulfate

potassium nitrite: potassium nitrite

A: 79-24-3
Nitroethane

B: 109-95-5
ethyl nitrite

C: 627-05-4
1-nitrobutane

...Expand

: 540-82-9
ethyl sulfate

sodium nitrite: sodium nitrite

A: 79-24-3
Nitroethane

B: 109-95-5
ethyl nitrite

C: 627-05-4
1-nitrobutane

...Expand

: 142-96-1
dibutyl ether

: 7697-37-2
nitric acid

A: 79-24-3
Nitroethane

B: 75-52-5
nitromethane

C: 627-05-4
1-nitrobutane

D: 108-03-2
1-Nitropropane

Conditions

Conditions	Yield
at 400℃; durch ein Glasrohr;Produkt 5:Butyl-nitrobutyl-aether;

...Expand

: 627-05-4
1-nitrobutane

: 298-12-4
Glyoxilic acid

: 367258-42-2
2-hydroxy-3-nitrohexanoic acid

Conditions

Conditions	Yield
With triethylamine In methanol; water at 0 - 20℃;	99%
With triethylamine In methanol at 0 - 20℃;	99%
With triethylamine In methanol at 0 - 20℃;	99%

: 627-05-4
1-nitrobutane

12percent nickel/Al-SBA-15 fiber: 12percent nickel/Al-SBA-15 fiber

: 109-73-9
N-butylamine

Conditions

Conditions	Yield
With hydrogen In ethanol at 109.84℃; under 18751.9 Torr; for 7.5h; Autoclave; Green chemistry; chemoselective reaction;	99%

: 627-05-4
1-nitrobutane

: 53055-05-3
3-methoxy 2-nitrobenzaldehyde

: 350821-45-3
1-(3-methoxy-2-nitrophenyl)-2-nitropentanol

Conditions

Conditions	Yield
With potassium fluoride; 18-crown-6 ether In isopropyl alcohol at 20℃; for 20h;	97%

: 627-05-4
1-nitrobutane

: 109-73-9
N-butylamine

Conditions

Conditions	Yield
Stage #1: 1-nitrobutane In water; acetonitrile at 20℃; for 0.0833333h; Stage #2: With sodium tetrahydroborate In water; acetonitrile at 20℃; for 0.333333h;	95%
Stage #1: 1-nitrobutane In water at 20℃; for 0.0166667h; Stage #2: With sodium tetrahydroborate In water at 50℃; for 0.166667h;	93%
With triethylamine In water at 80℃; for 6h; Inert atmosphere; Green chemistry; chemoselective reaction;	91%

: 1629-58-9
4-penten-3-one

: 627-05-4
1-nitrobutane

: 6-nitro-3-nonanone

Conditions

Conditions	Yield
With tri-n-octylmethylphosphonium hydrogen carbonate at 4℃; for 2h; Michael condensation;	95%
With triethylamine at 20℃; for 6h; Michael reaction;	83%
With cetyltrimethylammonium hydroxide at 20℃; for 1h; Michael reaction;	75%

: 627-05-4
1-nitrobutane

: ethyl 2-((tert-butoxycarbonyloxy)(phenyl)methyl)acrylate

: 1344660-46-3
(S,E)-ethyl 2-benzylidene-4-nitroheptanoate

Conditions

Conditions	Yield
With N-[3,5-bis(trifluoromethyl)phenyl]-N'-[(9R)-6'-methoxycinchonan-9-yl]thiourea In tetrahydrofuran at 20℃; for 48h; Neat (no solvent); optical yield given as %ee; enantioselective reaction;	95%

: 627-05-4
1-nitrobutane

: 624-48-6
dimethyl cis-but-2-ene-1,4-dioate

: 254098-83-4
dimethyl (E)-2-butylidenesuccinate

Conditions

Conditions	Yield
With 1,8-diazabicyclo[5.4.0]undec-7-ene In acetonitrile at 25℃; for 7h; Addition; Elimination;	94%

: 627-05-4
1-nitrobutane

: 78-94-4
methyl vinyl ketone

: 7404-75-3
(+/-)-1-(2-hydroxy-2-methyl-5-nitro-5-propylcyclohexyl)-1-ethanone

Conditions

Conditions	Yield
With potassium carbonate In water at 20℃; for 24h; Cycloaddition;	93%
With N-benzyl-trimethylammonium hydroxide; hydroquinone In 1,4-dioxane; methanol

: 627-05-4
1-nitrobutane

: 57020-97-0
ethyl 5-oxocyclopent-1-en-1-carboxylate

: 1236412-40-0
C12H19NO5

Conditions

Conditions	Yield
With quinine In toluene at -20℃; for 72h; Michael condensation; optical yield given as %ee; enantioselective reaction;	93%

: 627-05-4
1-nitrobutane

: 85217-69-2, 87802-71-9
cinnamyl methyl carbonate

: 1444826-33-8
(3R,4R)-(4-nitrohept-1-en-3-yl)benzene

Conditions

Conditions	Yield
With 1,4-diaza-bicyclo[2.2.2]octane; tris(dibenzylideneacetone)dipalladium(0) chloroform complex; C40H41FeN2O3P In tetrahydrofuran; dimethyl sulfoxide at 0℃; Inert atmosphere; enantioselective reaction;	93%

: 627-05-4
1-nitrobutane

: 104-88-1
4-chlorobenzaldehyde

: 1-Chloro-4-((E)-2-nitro-pent-1-enyl)-benzene

Conditions

Conditions	Yield
With CsNaX zeolite at 120℃; Condensation;	92%

: 120-57-0
piperonal

: 627-05-4
1-nitrobutane

: 104-94-9
4-methoxy-aniline

: 2-(benzo[d][1,3]dioxol-5-yl)-4-ethyl-6-methoxyquinoline

Conditions

Conditions	Yield
With iron(III) chloride at 90℃; for 6h; Sealed tube; regioselective reaction;	92%

...Expand

: C13H23N3O3

: 627-05-4
1-nitrobutane

: C17H32N4O5

Conditions

Conditions	Yield
Stage #1: 1-nitrobutane With sodium methylate at 20℃; for 0.25h; Stage #2: C13H23N3O3 at 20℃; for 1.5h; Michael addition; Further stages.;	91%

: 627-05-4
1-nitrobutane

: (R)-2-((benzyloxy)methyl)-2,4-dimethylcyclopent-4-ene-1,3-dione

: 303142-74-7
(S)-2-((benzyloxy)methyl)-4-butyl-2,5-dimethylcyclopent-4-ene-1,3-dione

Conditions

Conditions	Yield
With tetrabutylammomium bromide; potassium hydroxide In tetrahydrofuran at 20℃; for 1h; Inert atmosphere;	91%

: 627-05-4
1-nitrobutane

: 104-94-9
4-methoxy-aniline

: 1122-91-4
4-bromo-benzaldehyde

: 2-(4-bromophenyl)-4-ethyl-6-methoxyquinoline

Conditions

Conditions	Yield
With iron(III) chloride at 90℃; for 6h; Sealed tube; regioselective reaction;	91%

...Expand

: 627-05-4
1-nitrobutane

: N-butyl-N-propylhydroxylamine

Conditions

Conditions	Yield
With cerium(III) chloride In tetrahydrofuran at -40℃; for 0.5h; other nitroalkanes, other Grignard reagents, var. temp.;	90%

: 627-05-4
1-nitrobutane

CH3CH2CH2MgX: CH3CH2CH2MgX

: N-butyl-N-propylhydroxylamine

Conditions

Conditions	Yield
With cerium(III) chloride In tetrahydrofuran at -40℃; for 0.5h;	90%

: 627-05-4
1-nitrobutane

: 3858-78-4
n-butylamine hydrochloride

Conditions

Conditions	Yield
Stage #1: 1-nitrobutane With C36H56Cl3CrN2O; magnesium; 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane In tetrahydrofuran at 60℃; for 24h; Inert atmosphere; Schlenk technique; Stage #2: With hydrogenchloride In tetrahydrofuran; water; ethyl acetate at 20℃;	90%
Stage #1: 1-nitrobutane With hydrazine hydrate; zinc In methanol at 20℃; for 0.1h; Stage #2: With hydrogenchloride	75%
Stage #1: 1-nitrobutane With formic acid; nickel In methanol at 20℃; for 0.133333h; Reduction; Stage #2: With hydrogenchloride Addition;	60%

: C7H12N4O2

: 627-05-4
1-nitrobutane

: C11H21N5O4

Conditions

Conditions	Yield
Stage #1: 1-nitrobutane With sodium methylate at 20℃; for 0.25h; Stage #2: C7H12N4O2 at 20℃; for 1.5h; Michael addition; Further stages.;	90%

: 627-05-4
1-nitrobutane

: (S)-2-((benzyloxy)methyl)-2,4-dimethylcyclopent-4-ene-1,3-dione

: 1383003-83-5
(R)-2-((benzyloxy)methyl)-4-butyl-2,5-dimethylcyclopent-4-ene-1,3-dione

Conditions

Conditions	Yield
With tetrabutylammomium bromide; potassium hydroxide In tetrahydrofuran at 20℃; for 1h; Inert atmosphere;	90%

: 627-05-4
1-nitrobutane

: 104-88-1
4-chlorobenzaldehyde

: 104-94-9
4-methoxy-aniline

: 2-(4-chlorophenyl)-4-ethyl-6-methoxyquinoline

Conditions

Conditions	Yield
With iron(III) chloride at 90℃; for 6h; Sealed tube; regioselective reaction;	90%

...Expand

: C11H19N3O3

: 627-05-4
1-nitrobutane

: C15H28N4O5

Conditions

Conditions	Yield
Stage #1: 1-nitrobutane With sodium methylate at 20℃; for 0.25h; Stage #2: C11H19N3O3 at 20℃; for 0.5h; Michael addition; Further stages.;	89%

: 627-05-4
1-nitrobutane

: 100-52-7
benzaldehyde

: 62-53-3
aniline

: N-((1S,2R)-2-nitro-1-phenylpentyl)aniline

Conditions

Conditions	Yield
With N,N-dimethyl-cyclohexanamine; C23H25F6N3O3 In aq. acetate buffer at 0℃; for 5h; pH=5.5; Henry Nitro Aldol Condensation; stereoselective reaction;	89%

...Expand

: 627-05-4
1-nitrobutane

: 140-88-5
ethyl acrylate

: 120802-96-2
ethyl 3-propyl-4,5-dihydroisoxazole-5-carboxylate

Conditions

Conditions	Yield
With dmap; di-tert-butyl dicarbonate In acetonitrile at 25℃; for 5h;	89%

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