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627-05-4

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627-05-4 Usage

General Description

Colorless liquid.

Air & Water Reactions

Highly flammable. Slightly water soluble .

Reactivity Profile

Nitroalkanes, such as 1-NITROBUTANE, range from slight to strong oxidizing agents. If mixed with reducing agents, including hydrides, sulfides and nitrides, they may begin a vigorous reaction that culminates in a detonation. Nitroalkanes are milder oxidizing agents, but still react violently with reducing agents at higher temperature and pressures. Nitroalkanes react with inorganic bases to form explosive salts. The presence of metal oxides increases the thermal sensitivity of nitroalkanes. Nitroalkanes with more than one nitro group are generally explosive. Nitroalkanes are insoluble in water. Flammable/combustible material. May be ignited by heat, sparks or flames.

Check Digit Verification of cas no

The CAS Registry Mumber 627-05-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 627-05:
(5*6)+(4*2)+(3*7)+(2*0)+(1*5)=64
64 % 10 = 4
So 627-05-4 is a valid CAS Registry Number.
InChI:InChI=1/C4H9NO2/c1-2-3-4-5(6)7/h2-4H2,1H3

627-05-4 Well-known Company Product Price

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  • Aldrich

  • (259489)  1-Nitrobutane  98%

  • 627-05-4

  • 259489-5G

  • 3,477.24CNY

  • Detail

627-05-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Butane, 1-nitro-

1.2 Other means of identification

Product number -
Other names n-butylnitrit

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:627-05-4 SDS

627-05-4Synthetic route

1-bromo-butane
109-65-9

1-bromo-butane

1-nitrobutane
627-05-4

1-nitrobutane

Conditions
ConditionsYield
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
butyraldehyde oxime
110-69-0

butyraldehyde oxime

1-nitrobutane
627-05-4

1-nitrobutane

Conditions
ConditionsYield
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.
trans-4-Octene
14850-23-8

trans-4-Octene

A

1-nitrobutane
627-05-4

1-nitrobutane

B

butyric acid
107-92-6

butyric acid

Conditions
ConditionsYield
A 90%
B n/a
N-butylamine
109-73-9

N-butylamine

1-nitrobutane
627-05-4

1-nitrobutane

Conditions
ConditionsYield
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.
butyl magnesium bromide
693-04-9

butyl magnesium bromide

1-nitrobutane
627-05-4

1-nitrobutane

Conditions
ConditionsYield
With dinitrogen tetraoxide In tetrahydrofuran -190 deg C -> room temperature;71%
1-nitrobut-1-ene
27675-37-2, 3156-71-6

1-nitrobut-1-ene

1-nitrobutane
627-05-4

1-nitrobutane

Conditions
ConditionsYield
With sodium tetrahydroborate; silica gel In i-Amyl alcohol; chloroform at 20℃; for 2h; Inert atmosphere;59%
n-butyllithium
109-72-8, 29786-93-4

n-butyllithium

1-nitrobutane
627-05-4

1-nitrobutane

Conditions
ConditionsYield
With dinitrogen tetraoxide In tetrahydrofuran -190 deg C -> room temperature;19%
1-bromo-butane
109-65-9

1-bromo-butane

A

n-Butyl nitrite
544-16-1

n-Butyl nitrite

B

1-nitrobutane
627-05-4

1-nitrobutane

Conditions
ConditionsYield
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;
1-nitroethylene
3638-64-0

1-nitroethylene

ethylmagnesium bromide
925-90-6

ethylmagnesium bromide

1-nitrobutane
627-05-4

1-nitrobutane

Conditions
ConditionsYield
With diethyl ether
1-iodo-butane
542-69-8

1-iodo-butane

A

n-Butyl nitrite
544-16-1

n-Butyl nitrite

B

1-nitrobutane
627-05-4

1-nitrobutane

Conditions
ConditionsYield
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;
potassium ethyl sulfate
563-17-7

potassium ethyl sulfate

1-nitrobutane
627-05-4

1-nitrobutane

Conditions
ConditionsYield
With potassium nitrite
With sodium nitrite
n-butane
106-97-8

n-butane

A

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

2-nitrobutane

B

1-nitrobutane
627-05-4

1-nitrobutane

Conditions
ConditionsYield
With nitric acid at 420℃;
With nitric acid In water at 200℃; under 77574.3 Torr; for 0.0333333h; Product distribution / selectivity;
n-butane
106-97-8

n-butane

1-nitrobutane
627-05-4

1-nitrobutane

Conditions
ConditionsYield
With nitric acid at 400 - 440℃;
butyraldehyde oxime
110-69-0

butyraldehyde oxime

A

propyl cyanide
109-74-0

propyl cyanide

B

1-nitrobutane
627-05-4

1-nitrobutane

Conditions
ConditionsYield
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;
n-Butyl chloride
109-69-3

n-Butyl chloride

1-nitrobutane
627-05-4

1-nitrobutane

Conditions
ConditionsYield
With perhydrodibenzo-18-crown-6; potassium nitrite at 70℃; for 5h; Yield given;
Cyclopentane
287-92-3

Cyclopentane

A

formic acid
64-18-6

formic acid

B

ethene
74-85-1

ethene

C

1-nitrobutane
627-05-4

1-nitrobutane

D

1-Nitropropane
108-03-2

1-Nitropropane

E

nitrocyclopentane
2562-38-1

nitrocyclopentane

Conditions
ConditionsYield
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;
n-butane
106-97-8

n-butane

A

n-Butyl nitrite
544-16-1

n-Butyl nitrite

B

butyl nitrate
928-45-0

butyl nitrate

C

sec-butyl nitrite
924-43-6

sec-butyl nitrite

D

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

2-nitrobutane

E

2-butyl nitrate
924-52-7

2-butyl nitrate

F

1-nitrobutane
627-05-4

1-nitrobutane

Conditions
ConditionsYield
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.
N-butylamine
109-73-9

N-butylamine

A

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

(E)-1,2-dibutyldiazene 1,2-dioxide

B

n-Butylnitrit
44426-95-1

n-Butylnitrit

C

1-nitrobutane
627-05-4

1-nitrobutane

Conditions
ConditionsYield
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.
sodium butylsulfate
1000-67-5

sodium butylsulfate

1-nitrobutane
627-05-4

1-nitrobutane

Conditions
ConditionsYield
With potassium nitrate; sodium nitrite at 190℃; Yield given;
With potassium nitrate; sodium nitrite Thermodynamic data; Heating; E;
1-bromo-butane
109-65-9

1-bromo-butane

silver nitrite

silver nitrite

A

n-Butyl nitrite
544-16-1

n-Butyl nitrite

B

1-nitrobutane
627-05-4

1-nitrobutane

1-iodo-butane
542-69-8

1-iodo-butane

silver nitrite

silver nitrite

A

n-Butyl nitrite
544-16-1

n-Butyl nitrite

B

1-nitrobutane
627-05-4

1-nitrobutane

nitric acid
7697-37-2

nitric acid

n-butane
106-97-8

n-butane

A

Nitroethane
79-24-3

Nitroethane

B

nitromethane
75-52-5

nitromethane

C

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

2-nitrobutane

D

1-nitrobutane
627-05-4

1-nitrobutane

Conditions
ConditionsYield
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;
nitric acid
7697-37-2

nitric acid

n-butane
106-97-8

n-butane

A

Nitroethane
79-24-3

Nitroethane

B

nitromethane
75-52-5

nitromethane

C

1-nitrobutane
627-05-4

1-nitrobutane

D

1-Nitropropane
108-03-2

1-Nitropropane

Conditions
ConditionsYield
at 370 - 450℃; in der Gasphase;
nitric acid
7697-37-2

nitric acid

pentane
109-66-0

pentane

A

Nitroethane
79-24-3

Nitroethane

B

nitromethane
75-52-5

nitromethane

C

1-nitrobutane
627-05-4

1-nitrobutane

D

1-Nitropropane
108-03-2

1-Nitropropane

Conditions
ConditionsYield
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;
1-nitroethylene
3638-64-0

1-nitroethylene

diethyl ether
60-29-7

diethyl ether

ethylmagnesium bromide
925-90-6

ethylmagnesium bromide

A

1-nitrobutane
627-05-4

1-nitrobutane

B

hexanone-(3)-oxime

hexanone-(3)-oxime

Conditions
ConditionsYield
at 10 - 15℃; und bei folgendem Kochen;
standardbutyl iodide

standardbutyl iodide

1-nitrobutane
627-05-4

1-nitrobutane

Conditions
ConditionsYield
With silver(I) nitrite
ethyl sulfate
540-82-9

ethyl sulfate

potassium nitrite

potassium nitrite

A

Nitroethane
79-24-3

Nitroethane

B

ethyl nitrite
109-95-5

ethyl nitrite

C

1-nitrobutane
627-05-4

1-nitrobutane

ethyl sulfate
540-82-9

ethyl sulfate

sodium nitrite

sodium nitrite

A

Nitroethane
79-24-3

Nitroethane

B

ethyl nitrite
109-95-5

ethyl nitrite

C

1-nitrobutane
627-05-4

1-nitrobutane

dibutyl ether
142-96-1

dibutyl ether

nitric acid
7697-37-2

nitric acid

A

Nitroethane
79-24-3

Nitroethane

B

nitromethane
75-52-5

nitromethane

C

1-nitrobutane
627-05-4

1-nitrobutane

D

1-Nitropropane
108-03-2

1-Nitropropane

Conditions
ConditionsYield
at 400℃; durch ein Glasrohr;Produkt 5:Butyl-nitrobutyl-aether;
1-nitrobutane
627-05-4

1-nitrobutane

Glyoxilic acid
298-12-4

Glyoxilic acid

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

2-hydroxy-3-nitrohexanoic acid

Conditions
ConditionsYield
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%
1-nitrobutane
627-05-4

1-nitrobutane

12percent nickel/Al-SBA-15 fiber

12percent nickel/Al-SBA-15 fiber

N-butylamine
109-73-9

N-butylamine

Conditions
ConditionsYield
With hydrogen In ethanol at 109.84℃; under 18751.9 Torr; for 7.5h; Autoclave; Green chemistry; chemoselective reaction;99%
1-nitrobutane
627-05-4

1-nitrobutane

3-methoxy 2-nitrobenzaldehyde
53055-05-3

3-methoxy 2-nitrobenzaldehyde

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

1-(3-methoxy-2-nitrophenyl)-2-nitropentanol

Conditions
ConditionsYield
With potassium fluoride; 18-crown-6 ether In isopropyl alcohol at 20℃; for 20h;97%
1-nitrobutane
627-05-4

1-nitrobutane

N-butylamine
109-73-9

N-butylamine

Conditions
ConditionsYield
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%
4-penten-3-one
1629-58-9

4-penten-3-one

1-nitrobutane
627-05-4

1-nitrobutane

6-nitro-3-nonanone

6-nitro-3-nonanone

Conditions
ConditionsYield
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%
1-nitrobutane
627-05-4

1-nitrobutane

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

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

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

(S,E)-ethyl 2-benzylidene-4-nitroheptanoate

Conditions
ConditionsYield
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%
1-nitrobutane
627-05-4

1-nitrobutane

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

dimethyl cis-but-2-ene-1,4-dioate

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

dimethyl (E)-2-butylidenesuccinate

Conditions
ConditionsYield
With 1,8-diazabicyclo[5.4.0]undec-7-ene In acetonitrile at 25℃; for 7h; Addition; Elimination;94%
1-nitrobutane
627-05-4

1-nitrobutane

methyl vinyl ketone
78-94-4

methyl vinyl ketone

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

(+/-)-1-(2-hydroxy-2-methyl-5-nitro-5-propylcyclohexyl)-1-ethanone

Conditions
ConditionsYield
With potassium carbonate In water at 20℃; for 24h; Cycloaddition;93%
With N-benzyl-trimethylammonium hydroxide; hydroquinone In 1,4-dioxane; methanol
1-nitrobutane
627-05-4

1-nitrobutane

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

ethyl 5-oxocyclopent-1-en-1-carboxylate

C12H19NO5
1236412-40-0

C12H19NO5

Conditions
ConditionsYield
With quinine In toluene at -20℃; for 72h; Michael condensation; optical yield given as %ee; enantioselective reaction;93%
1-nitrobutane
627-05-4

1-nitrobutane

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

cinnamyl methyl carbonate

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

(3R,4R)-(4-nitrohept-1-en-3-yl)benzene

Conditions
ConditionsYield
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%
1-nitrobutane
627-05-4

1-nitrobutane

4-chlorobenzaldehyde
104-88-1

4-chlorobenzaldehyde

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

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

Conditions
ConditionsYield
With CsNaX zeolite at 120℃; Condensation;92%
piperonal
120-57-0

piperonal

1-nitrobutane
627-05-4

1-nitrobutane

4-methoxy-aniline
104-94-9

4-methoxy-aniline

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

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

Conditions
ConditionsYield
With iron(III) chloride at 90℃; for 6h; Sealed tube; regioselective reaction;92%
C13H23N3O3

C13H23N3O3

1-nitrobutane
627-05-4

1-nitrobutane

C17H32N4O5

C17H32N4O5

Conditions
ConditionsYield
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%
1-nitrobutane
627-05-4

1-nitrobutane

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

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

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

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

Conditions
ConditionsYield
With tetrabutylammomium bromide; potassium hydroxide In tetrahydrofuran at 20℃; for 1h; Inert atmosphere;91%
1-nitrobutane
627-05-4

1-nitrobutane

4-methoxy-aniline
104-94-9

4-methoxy-aniline

4-bromo-benzaldehyde
1122-91-4

4-bromo-benzaldehyde

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

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

Conditions
ConditionsYield
With iron(III) chloride at 90℃; for 6h; Sealed tube; regioselective reaction;91%
1-nitrobutane
627-05-4

1-nitrobutane

N-butyl-N-propylhydroxylamine

N-butyl-N-propylhydroxylamine

Conditions
ConditionsYield
With cerium(III) chloride In tetrahydrofuran at -40℃; for 0.5h; other nitroalkanes, other Grignard reagents, var. temp.;90%
1-nitrobutane
627-05-4

1-nitrobutane

CH3CH2CH2MgX

CH3CH2CH2MgX

N-butyl-N-propylhydroxylamine

N-butyl-N-propylhydroxylamine

Conditions
ConditionsYield
With cerium(III) chloride In tetrahydrofuran at -40℃; for 0.5h;90%
1-nitrobutane
627-05-4

1-nitrobutane

n-butylamine hydrochloride
3858-78-4

n-butylamine hydrochloride

Conditions
ConditionsYield
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

C7H12N4O2

1-nitrobutane
627-05-4

1-nitrobutane

C11H21N5O4

C11H21N5O4

Conditions
ConditionsYield
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%
1-nitrobutane
627-05-4

1-nitrobutane

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

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

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

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

Conditions
ConditionsYield
With tetrabutylammomium bromide; potassium hydroxide In tetrahydrofuran at 20℃; for 1h; Inert atmosphere;90%
1-nitrobutane
627-05-4

1-nitrobutane

4-chlorobenzaldehyde
104-88-1

4-chlorobenzaldehyde

4-methoxy-aniline
104-94-9

4-methoxy-aniline

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

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

Conditions
ConditionsYield
With iron(III) chloride at 90℃; for 6h; Sealed tube; regioselective reaction;90%
C11H19N3O3

C11H19N3O3

1-nitrobutane
627-05-4

1-nitrobutane

C15H28N4O5

C15H28N4O5

Conditions
ConditionsYield
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%
1-nitrobutane
627-05-4

1-nitrobutane

benzaldehyde
100-52-7

benzaldehyde

aniline
62-53-3

aniline

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

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

Conditions
ConditionsYield
With N,N-dimethyl-cyclohexanamine; C23H25F6N3O3 In aq. acetate buffer at 0℃; for 5h; pH=5.5; Henry Nitro Aldol Condensation; stereoselective reaction;89%
1-nitrobutane
627-05-4

1-nitrobutane

ethyl acrylate
140-88-5

ethyl acrylate

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

ethyl 3-propyl-4,5-dihydroisoxazole-5-carboxylate

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

627-05-4Relevant articles and documents

Green synthesis of low-carbon chain nitroalkanes via a novel tandem reaction of ketones catalyzed by TS-1

Chu, Qingyan,He, Guangke,Xi, Yang,Wang, Ping,Yu, Haoxuan,Liu, Rui,Zhu, Hongjun

, p. 46 - 50 (2018/02/09)

A green and efficient one-pot method has been developed for the synthesis of low-carbon chain nitroalkanes via a novel TS-1 catalyzed tandem oxidation of ketones with H2O2 and NH3. The tandem reaction including ammoxidation, oximation and oxidation of oximes, afforded up to 88% yield and 98% chemo-selectivity requiring only 90 min, at 70 °C and atmospheric pressure. Moreover, this method was even amenable to 100-fold scale-up without loss of chemical efficiency with 87% yield, represents a significant advance towards industrial production of nitroalkanes. Furthermore, the plausible mechanism of TS-1 catalyzed tandem oxidation of ketones to prepare nitroalkanes was proposed.

BIS-HETEROARYL DERIVATIVES AS MODULATORS OF PROTEIN AGGREGATION

-

Paragraph 0203, (2017/02/24)

The present invention relates to certain bis-heteroaryl compounds, pharmaceutical compositions containing them, and methods of using them, including methods for preventing, reversing, slowing, or inhibiting protein aggregation, and methods of treating diseases that are associated with protein aggregation, including neurodegenerative diseases such as Parkinson's disease, Alzheimer's disease, Lewy body disease, Parkinson's disease with dementia, fronto- temporal dementia, Huntington's Disease, amyotrophic lateral sclerosis, and multiple system atrophy, and cancer including melanoma.

Core-shell palladium nanoparticle@metal-organic frameworks as multifunctional catalysts for cascade reactions

Zhao, Meiting,Deng, Ke,He, Liangcan,Liu, Yong,Li, Guodong,Zhao, Huijun,Tang, Zhiyong

supporting information, p. 1738 - 1741 (2014/03/21)

Uniform core-shell Pd@IRMOF-3 nanostructures, where single Pd nanoparticle core is surrounded by amino-functionalized IRMOF-3 shell, are prepared by a facile mixed solvothermal method. When used as multifunctional catalysts, the Pd@IRMOF-3 nanocomposites exhibit high activity, enhanced selectivity, and excellent stability in the cascade reaction. Both experimental evidence and theoretical calculations reveal that the high catalytic performance of Pd@IRMOF-3 nanocomposites originates from their unique core-shell structures.

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