CAS No.75-04-7,Ethylamine Suppliers

: 75-05-8
acetonitrile

: 75-04-7
ethylamine

Conditions

Conditions	Yield
With sodium tetrahydroborate In water; dimethyl sulfoxide at 60℃; for 4.5h; High pressure; Green chemistry;	99.9%
With borane-ammonia complex; copper cobaltite In methanol; water at 50℃; under 1125.11 Torr; for 5h; Catalytic behavior; Reagent/catalyst; Pressure; Concentration; Sealed tube;	98%
With hydrogen In ethanol at 99.84℃; under 22502.3 Torr; Autoclave;	81%

: 79-24-3
Nitroethane

: 75-04-7
ethylamine

Conditions

Conditions	Yield
With borane-ammonia complex In methanol; water at 20℃; for 0.0833333h;	99%
With ammonia borane; Pd/MIL-101 In methanol; water at 20℃; for 0.025h;	99%
With sodium tetrahydroborate In methanol; water at 20℃; for 0.0666667h; Sealed tube; Green chemistry;	99%

: 79-24-3
Nitroethane

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

: 75-04-7
ethylamine

Conditions

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

: 107-12-0
propiononitrile

: 75-04-7
ethylamine

Conditions

Conditions	Yield
Stage #1: propiononitrile In methanol; water at 20℃; for 0.0833333h; Stage #2: With ammonia borane In methanol; water at 20℃;	98%

: 79-24-3
Nitroethane

A: 75-04-7
ethylamine

B: 624-81-7
ethylhydroxylamine

Conditions

Conditions	Yield
With hydrogen In para-xylene; isopropyl alcohol at 25℃; under 760.051 Torr; for 2h; Catalytic behavior; Reagent/catalyst;	A 6% B 94%
Pt-Rh catalysts Product distribution; electrochemical reduction;
With sulfuric acid; palladium Product distribution; electrocatalytic hydrogenation, oth. catalysts;
With 5% Pd/SiO2; hydrogen In isopropyl alcohol at 20℃; under 750.075 Torr; for 2h;	A 9 %Spectr. B 91 %Spectr.

: 5300-22-1
(R/S)-2-(ethylamino)-1-phenylethanol

A: 52500-61-5
2-hydroxy-1-phenylpropylamine

B: 50-00-0
formaldehyd

C: 100-52-7
benzaldehyde

D: 75-04-7
ethylamine

E: 75-07-0
acetaldehyde

Conditions

Conditions	Yield
With water at 25℃; Product distribution; Mechanism; anodic oxidation, carbonate buffer, pH 10; effect of substituents investigated with different types of β-alkanolamines;	A 1.9% B 67% C 75% D 79% E 10%

...Expand

: 3710-84-7
N-ethyl-N-hydroxy-ethanamine

A: 50-00-0
formaldehyd

B: 624-78-2
N-Ethylmethylamine

C: 75-04-7
ethylamine

D: 75-07-0
acetaldehyde

Conditions

Conditions	Yield
With phosphorus pentachloride In toluene at 18 - 20℃; Mechanism; Product distribution; object of study: Stieglitz rearrangement (prototype);	A n/a B 1.4% C 76% D n/a

...Expand

: 19528-69-9
{(C2H5NH2)2BH2}(1+)*{SC2H5}(1-)={(C2H5NH2)2BH2}{SC2H5}

A: 7360-03-4
N,N',N''-triethylborazine

B: 75-04-7
ethylamine

C: 856627-30-0
ethylamine borane complex

D: 75-08-1
ethanethiol

Conditions

Conditions	Yield
In neat (no solvent) pyrolysis;;	A 20% B n/a C 36% D 75%
In neat (no solvent)

...Expand

: 100-37-8
2-(Diethylamino)ethanol

A: 50-00-0
formaldehyd

B: 75-04-7
ethylamine

C: 75-07-0
acetaldehyde

D: 109-89-7
diethylamine

E: 110-73-6
2-(Ethylamino)ethanol

Conditions

Conditions	Yield
With water at 25℃; Product distribution; Mechanism; anodic oxidation, carbonate buffer, pH 10; effect of substituents investigated with different types of β-alkanolamines;	A 5% B 1.6% C 72% D 20% E 73%

...Expand

: 623-76-7
N,N'-diethylurea

: 18522-92-4
sodium p-toluenesulfonamide

A: 1467-23-8
N-(ethylcarbamoyl)-4-methylbenzenesulfonamide

B: 75-04-7
ethylamine

Conditions

Conditions	Yield
at 145℃; for 5h; Product distribution; other time;;	A 71.6% B n/a
at 145℃; for 5h;	A 71.6% B n/a

...Expand

: 82922-12-1
2-Diethylamino-pentan-3-ol

A: 75-04-7
ethylamine

B: 75-07-0
acetaldehyde

C: 123-38-6
propionaldehyde

: 100910-76-7
2-Ethylamino-pentan-3-ol

E: 109-89-7
diethylamine

Conditions

Conditions	Yield
With water at 25℃; Product distribution; Mechanism; anodic oxidation, carbonate buffer, pH 10; effect of substituents investigated with different types of β-alkanolamines;	A n/a B 70% C 36% D n/a E 46%

...Expand

: 82922-13-2
2-(ethylamino)-2-methylpropanol hydrochloride

A: 50-00-0
formaldehyd

B: 75-04-7
ethylamine

C: 124-68-5
2-Amino-2-methyl-1-propanol

D: 75-07-0
acetaldehyde

E: 67-64-1
acetone

Conditions

Conditions	Yield
With water at 25℃; Product distribution; Mechanism; anodic oxidation, carbonate buffer, pH 10; effect of substituents investigated with different types of β-alkanolamines;	A 50% B 44% C 14% D 26% E 66%

...Expand

: 82922-13-2
2-(ethylamino)-2-methylpropanol hydrochloride

A: 50-00-0
formaldehyd

B: 75-04-7
ethylamine

C: 124-68-5
2-Amino-2-methyl-1-propanol

D: 67-64-1
acetone

Conditions

Conditions	Yield
With water at 25℃; anodic oxidation, pH 10, carbonate buffer; Further byproducts given;	A 50% B 44% C 14% D 66%

...Expand

: 107-29-9
Acetaldehyde oxime

: 75-04-7
ethylamine

Conditions

Conditions	Yield
With ammonium formate; zinc In methanol for 0.05h; Heating;	62%
With ammonium amalgam
With ammonium formate; magnesium In methanol at 20℃; for 0.666667h;

: 2683-58-1
1-diethylamino-butan-2-ol

A: 50-00-0
formaldehyd

B: 68058-17-3
1-ethylamino-butan-2-ol

C: 75-04-7
ethylamine

D: 75-07-0
acetaldehyde

E: 123-38-6
propionaldehyde

F: 109-89-7
diethylamine

Conditions

Conditions	Yield
With water at 25℃; Product distribution; Mechanism; anodic oxidation, carbonate buffer, pH 10; effect of substituents investigated with different types of β-alkanolamines;	A 17% B 59% C 3% D 60% E 18% F 32%

...Expand

: trans-bisdinitrogenbis(1,2-diphenylphosphinoethane)molybdenum(0)

: 55-18-5
N-Nitrosodiethylamine

A: 74-85-1
ethene

: trans-bis[1,2-bis(diphenylphosphino)ethane]hydroxo(nitrosyl)molybdenum-tetrahydrofuran (1/2)

C: 7727-37-9
nitrogen

D: 75-04-7
ethylamine

Conditions

Conditions	Yield
With K2CO3; THF In tetrahydrofuran Irradiation (UV/VIS); Et2NNO and K2CO3 added to soln. of Mo complex in THF, heated under reflux under N2 with W-light irrdn. for 4 h; filtered hot, cooled to room temp., crystals recrystd. from THF; elem. anal.;	A n/a B 60% C n/a D n/a

...Expand

: 38451-07-9
1,6-diethyl-2,5-dithiobiurea

A: 75-04-7
ethylamine

B: 13625-52-0
4-ethyl-[1,2,4]triazolidine-3,5-dithione

Conditions

Conditions	Yield
With sodium hydroxide In water Heating;	A n/a B 56%

: 86465-00-1
1-Ethoxy-3-ethylamino-propan-2-ol

A: 50-00-0
formaldehyd

B: 75-04-7
ethylamine

C: 75-07-0
acetaldehyde

Conditions

Conditions	Yield
With chlorine dioxide In water for 1h; Product distribution; Ambient temperature;	A 4% B 55% C 53%

...Expand

: 86464-98-4
1-Cyclohexyloxy-3-ethylamino-propan-2-ol

A: 50-00-0
formaldehyd

B: 75-04-7
ethylamine

C: 75-07-0
acetaldehyde

D: 108-93-0
cyclohexanol

Conditions

Conditions	Yield
With chlorine dioxide In water for 1h; Product distribution; Ambient temperature;	A 5% B 54% C 55% D 18%

...Expand

: 58461-93-1
1-ethylamino-3-phenoxy-propan-2-ol

A: 50-00-0
formaldehyd

B: 75-04-7
ethylamine

C: 75-07-0
acetaldehyde

D: 108-95-2
phenol

Conditions

Conditions	Yield
With chlorine dioxide In water for 1h; Product distribution; Ambient temperature;	A 3% B 49% C 50% D 30%

...Expand

: 64-17-5
ethanol

: 112-53-8
1-dodecyl alcohol

: 75-05-8
acetonitrile

A: 112-40-3
dodecane

B: 74-84-0
ethane

C: 35902-57-9
N-n-dodecyl-ethylamine

D: 4271-27-6
diethyllaurylamine

E: 75-04-7
ethylamine

F: 121-44-8
triethylamine

Conditions

Conditions	Yield
With hydrogen; aluminum oxide; copper at 240℃; under 7600 Torr; Product distribution; other catalyst and composition;	A n/a B n/a C 15% D 30% E n/a F 50%

...Expand

: 110-73-6
2-(Ethylamino)ethanol

A: 50-00-0
formaldehyd

B: 75-04-7
ethylamine

C: 141-43-5
ethanolamine

D: 75-07-0
acetaldehyde

Conditions

Conditions	Yield
With water at 25℃; anodic oxidation, pH 10, carbonate buffer; Further byproducts given;	A 14% B 43% C 45% D 44%

...Expand

: 110-73-6
2-(Ethylamino)ethanol

A: 50-00-0
formaldehyd

B: 75-04-7
ethylamine

C: 141-43-5
ethanolamine

D: 75-07-0
acetaldehyde

E: 141-46-8
Glycolaldehyde

Conditions

Conditions	Yield
With water at 25℃; Product distribution; Mechanism; anodic oxidation, carbonate buffer, pH 10; effect of substituents investigated with different types of β-alkanolamines;	A 14% B 43% C 45% D 44% E n/a

...Expand

: 125908-31-8
1-ethyl-6-tolyl-2,5-dithiobiurea

A: 14731-25-0
2-(4'-methylphenylamino)-Δ2-1,3,4-thiadiazoline-5-thione

B: 106-49-0
p-toluidine

C: 75-04-7
ethylamine

D: 13625-52-0
4-ethyl-[1,2,4]triazolidine-3,5-dithione

Conditions

Conditions	Yield
With sodium hydroxide In water Heating;	A 44% B n/a C n/a D 31%

...Expand

: 73825-96-4
1-(ethylamino)-2-methylpropan-2-ol

A: 75-04-7
ethylamine

B: 2854-16-2
1-Amino-2-methyl-propan-2-ol

C: 75-07-0
acetaldehyde

D: 67-64-1
acetone

Conditions

Conditions	Yield
With water at 25℃; anodic oxidation, pH 10, carbonate buffer; Further byproducts given;	A 35% B 18% C 34% D 43%

...Expand

: 73825-96-4
1-(ethylamino)-2-methylpropan-2-ol

A: 50-00-0
formaldehyd

B: 75-04-7
ethylamine

C: 2854-16-2
1-Amino-2-methyl-propan-2-ol

D: 75-07-0
acetaldehyde

E: 67-64-1
acetone

Conditions

Conditions	Yield
With water at 25℃; Product distribution; Mechanism; anodic oxidation, carbonate buffer, pH 10; effect of substituents investigated with different types of β-alkanolamines;	A 18% B 35% C 18% D 34% E 43%

...Expand

: 125908-34-1
1-ethyl-6-(4'-ethoxyphenyl)-2,5-dithiobiurea

A: 68161-60-4
2-(4'-ethoxyphenylamino)-Δ2-1,3,4-thiadiazoline-5-thione

B: 75-04-7
ethylamine

C: 156-43-4
4-Ethoxyaniline

D: 13625-52-0
4-ethyl-[1,2,4]triazolidine-3,5-dithione

Conditions

Conditions	Yield
With sodium hydroxide In water Heating;	A 41% B n/a C n/a D 32%

...Expand

: 125908-33-0
1-ethyl-6-(4'-methoxyphenyl)-2,5-dithiobiurea

A: 37844-24-9
2-(4'-methoxyphenylamino)-Δ2-1,3,4-thiadiazoline-5-thione

B: 104-94-9
4-methoxy-aniline

C: 75-04-7
ethylamine

D: 13625-52-0
4-ethyl-[1,2,4]triazolidine-3,5-dithione

Conditions

Conditions	Yield
With sodium hydroxide In water Heating;	A 40% B n/a C n/a D 34%

...Expand

: 61784-88-1
1-ethyl-6-phenyl-2,5-dithiobiurea

A: 75-04-7
ethylamine

B: 62-53-3
aniline

C: 10253-83-5
5-phenylamino-3H-[1,3,4]thiadiazole-2-thione

D: 13625-52-0
4-ethyl-[1,2,4]triazolidine-3,5-dithione

Conditions

Conditions	Yield
With sodium hydroxide In water Heating;	A n/a B n/a C 38% D 33%

...Expand

: 123-56-8
Succinimide

: 75-04-7
ethylamine

: 3025-98-7
N-ethyl-succinic diamide

Conditions

Conditions	Yield
at 20℃; under 600.048 - 750.06 Torr; Addition; soid-gas reaction; ring cleavage;	100%
With water

: 5022-29-7
N-ethylphthalimide

: 75-04-7
ethylamine

: 22011-24-1
N,N'-diethylphthalic diamide

Conditions

Conditions	Yield
at 20℃; under 600.048 - 750.06 Torr; Addition; solid-gas reaction; ring cleavage;	100%

: 555-16-8
4-nitrobenzaldehdye

: 75-04-7
ethylamine

: 25105-58-2
N-(p-nitrobenzylidene)ethylamine

Conditions

Conditions	Yield
at 20℃; under 750.06 Torr; Solid phase reaction; gas-solid reaction;	100%
With water
In ethanol at 50℃;
In tetrahydrofuran; ethanol at 20℃; for 12h; Inert atmosphere;
In ethanol at 20℃; for 12h;

: 3460-18-2
1,4-dibromo-2-nitrobenzene

: 75-04-7
ethylamine

: 56136-82-4
(4-bromo-2-nitrophenyl)ethylamine

Conditions

Conditions	Yield
In water at 100℃; for 24h; Sealed vessel;	100%

: 459-57-4
4-fluorobenzaldehyde

: 75-04-7
ethylamine

: 82605-86-5
(E)-N-(4-fluorobenzylidene)ethanamine

Conditions

Conditions	Yield
With magnesium sulfate In dichloromethane; water at 24.84℃; for 4h;	100%
In diethyl ether for 2h;	74%

: 100-44-7
benzyl chloride

: 75-04-7
ethylamine

: 14321-27-8
N-ethylbenzylamine

Conditions

Conditions	Yield
	100%

: 99735-46-3
methyl (3S)-1-<(R)-1-phenylethyl>-5-oxo-3-pyrrolidinecarboxylate

: 75-04-7
ethylamine

: (S)-5-Oxo-1-((R)-1-phenyl-ethyl)-pyrrolidine-3-carboxylic acid ethylamide

Conditions

Conditions	Yield
In water at -10℃; for 1h;	100%

: 115975-33-2
N,N-Dimethyl-2,4-bis(trifluoroacetyl)-1-naphthylamine

: 75-04-7
ethylamine

: 115975-37-6
1-[1-Ethylamino-4-(2,2,2-trifluoro-acetyl)-naphthalen-2-yl]-2,2,2-trifluoro-ethanone

Conditions

Conditions	Yield
In water; acetonitrile for 2h; Ambient temperature;	100%

: 75-04-7
ethylamine

: 84054-96-6
ethyl 4-formyl-2-hydroxybenzoate

: 84054-99-9
4-[(Z)-Ethyliminomethyl]-2-hydroxy-benzoic acid ethyl ester

Conditions

Conditions	Yield
for 0.333333h;	100%

: 75-04-7
ethylamine

: 100890-40-2
1-Methyl-6-methylsulfanyl-2,4-dioxo-3-phenyl-1,2,3,4-tetrahydro-pyrimidine-5-carbonitrile

: 105736-29-6
6-Ethylamino-1-methyl-2,4-dioxo-3-phenyl-1,2,3,4-tetrahydro-pyrimidine-5-carbonitrile

Conditions

Conditions	Yield
In acetonitrile for 0.0833333h; Ambient temperature;	100%

: 75-04-7
ethylamine

: 2,4,6,8-Tetrachloro-N,N''-diethyl-N',N',N''',N'''-tetramethyl-2λ5,4λ5,6λ5,8λ5-[1,3,5,7,2,4,6,8]tetrazatetraphosphocine-2,4,6,8-tetraamine

: C16H48N12P4

Conditions

Conditions	Yield
In diethyl ether Heating;	100%

: 75-04-7
ethylamine

: N,N''-Di-tert-butyl-2,4,6,8-tetrachloro-N',N'''-diethyl-2λ5,4λ5,6λ5,8λ5-[1,3,5,7,2,4,6,8]tetrazatetraphosphocine-2,4,6,8-tetraamine

: C20H56N12P4

Conditions

Conditions	Yield
In diethyl ether Heating;	100%

: 75-04-7
ethylamine

: 2,4,6,8-Tetrachloro-N,N''-diethyl-N',N'''-dimethyl-N',N'''-diphenyl-2λ5,4λ5,6λ5,8λ5-[1,3,5,7,2,4,6,8]tetrazatetraphosphocine-2,4,6,8-tetraamine

: C26H52N12P4

Conditions

Conditions	Yield
In diethyl ether Heating;	100%

: 75-04-7
ethylamine

: 22113-86-6
ethylammonium nitrate

Conditions

Conditions	Yield
With nitric acid In water at 10℃; pH=7.3;	100%
With nitric acid In water for 1h; pH=7.3; Cooling with ice;	100%
With acide nitrique at 0℃;

: 27210-68-0
1-diethylamino-2,4-dinitronaphthalene

: 75-04-7
ethylamine

A: 27210-67-9
N-ethyl-2,4-dinitro-1-naphthylamine

B: 109-89-7
diethylamine

Conditions

Conditions	Yield
In water at 30℃; for 1h;	A 100% B n/a

...Expand

: 75-04-7
ethylamine

: 168697-54-9
tetraethyl ethylenebisbenzoyloxymalonate

: tetraethylamide of 1,2-ethylenebistartronic acid

Conditions

Conditions	Yield
In methanol at 20℃; for 72h;	100%

: 23596-82-9
3,4-bis(diphenylmethylene)-1,2-cyclobutanedione

: 75-04-7
ethylamine

: N-ethyl-3,4-bis(diphenylmethylene)succinimide

Conditions

Conditions	Yield
With bromine In tetrachloromethane for 0.5h; Ambient temperature;	100%

: 75-04-7
ethylamine

: 221636-53-9
N,N-dimethyl-5,7-bis(trifluoroacetyl)-8-quinolylamine

: 1-[8-Ethylamino-5-(2,2,2-trifluoro-acetyl)-quinolin-7-yl]-2,2,2-trifluoro-ethanone

Conditions

Conditions	Yield
With water In acetonitrile for 1h; Ambient temperature;	100%
With water In acetonitrile at 20℃; for 1h; Substitution;	100%

: 96-48-0
4-butanolide

: 75-04-7
ethylamine

: 42042-64-8
N-ethyl-4-hydroxybutanamide

Conditions

Conditions	Yield
In tetrahydrofuran at 50℃; for 22h;	100%
In tetrahydrofuran at 20℃; Acylation;
With ammonia In methanol at 20℃;

: 1121-89-7
piperidine-2,6-dione

: 75-04-7
ethylamine

: N-ethyl-glutaric diamide

Conditions

Conditions	Yield
at 80℃; under 600.048 - 750.06 Torr; Addition; soid-gas reaction; ring cleavage;	100%

: 524-38-9
N-hydroxyphthalimide

: 75-04-7
ethylamine

: 22011-24-1
N,N'-diethylphthalic diamide

Conditions

Conditions	Yield
at 20℃; under 600.048 - 750.06 Torr; Addition; solid-gas reaction; ring cleavage;	100%

: 4702-13-0
N-phthaloylglycine

: 75-04-7
ethylamine

: 22011-24-1
N,N'-diethylphthalic diamide

Conditions

Conditions	Yield
at 20℃; under 600.048 - 750.06 Torr; Substitution; solid-gas reaction; ring cleavage;	100%

: 117-08-8
tetrachlorophthalic anhydride

: 75-04-7
ethylamine

: ethyl-tetrachlorophthalamic acid ethylammonium salt

Conditions

Conditions	Yield
under 750.06 Torr; Condensation; solid-gas reaction; ring cleavage;	100%

: 119-84-6
C6H4(CH2CH2C(O)O)

: 75-04-7
ethylamine

: ethyl-3-(2-hydroxyphenyl)-propionamide

Conditions

Conditions	Yield
at 0℃; under 150.012 Torr; Addition; solid-gas reaction; ring cleavage;	100%

: 123-08-0
4-hydroxy-benzaldehyde

: 75-04-7
ethylamine

: 4-[(ethylimino)methyl]phenol

Conditions

Conditions	Yield
at 0℃; under 187.515 Torr; Solid phase reaction; gas-solid reaction;	100%
With calcium oxide In ethanol; water at 20℃; for 2.5h;

: 21240-34-6
4,5-diphenyl-1,3-dioxol-2-one

: 75-04-7
ethylamine

: ethylcarbamic 1-phenylphenacylester

Conditions

Conditions	Yield
at 20℃; under 600.048 Torr; for 24h; Addition; solid-gas reaction; ring cleavage;	100%

: 75-04-7
ethylamine

: 556-61-6
methyl thioisocyanate

: 2489-77-2
1,1,3-trimethylthiourea

Conditions

Conditions	Yield
at 0℃; under 375.03 Torr; Addition; solid-gas reaction;	100%

: 75-04-7
ethylamine

: 100-10-7
4-dimethylamino-benzaldehyde

: 59488-00-5
4-[(ethylimino)methyl]-N,N-dimethylbenzeneamine

Conditions

Conditions	Yield
at 20℃; under 750.06 Torr; Solid phase reaction; gas-solid reaction;	100%

: 75-04-7
ethylamine

: 551-06-4
1-isothiocyanatonaphthalene

: 2742-61-2
1,1-dimethyl-3-naphthalene-1-yl-thiourea

Conditions

Conditions	Yield
at 20℃; under 750.06 Torr; Addition; solid-gas reaction;	100%

: 75-04-7
ethylamine

: 642-31-9
9-anthracene aldehyde

: [1-Anthracen-9-yl-meth-(Z)-ylidene]-ethyl-amine

Conditions

Conditions	Yield
at 20℃; under 750.06 Torr; Solid phase reaction; gas-solid reaction;	100%
In methanol for 9h; Reflux;	84%

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