Product Name

  • Name

    3-Amino-5-methylisoxazole

  • EINECS 214-013-6
  • CAS No. 1072-67-9
  • Article Data22
  • CAS DataBase
  • Density 1.167 g/cm3
  • Solubility soluble in water
  • Melting Point 59-63 °C
  • Formula C4H6N2O
  • Boiling Point 235.9 °C at 760 mmHg
  • Molecular Weight 98.1044
  • Flash Point 96.5 °C
  • Transport Information
  • Appearance slightly yellow flakes
  • Safety 22-24/25-47-37/39-26-16-26/37/39/47-36
  • Risk Codes 5-36/37/38-11-36/37/38/5-20/21/22
  • Molecular Structure Molecular Structure of 1072-67-9 (3-Amino-5-methylisoxazole)
  • Hazard Symbols FlammableF,IrritantXi
  • Synonyms Isoxazole,3-amino-5-methyl- (6CI,7CI,8CI);5-Methyl-1,2-oxazol-3-amine;5-Methyl-3-aminoisoxazole;5-Methyl-3-isoxazolamine;5-Methyl-3-isoxazolylamine;NSC 159134;3-amino-5-methylisooxzole;
  • PSA 52.05000
  • LogP 1.14640

Synthetic route

C11H13N3O2S

C11H13N3O2S

5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

Conditions
ConditionsYield
Stage #1: C11H13N3O2S With hydroxylamine hydrochloride; potassium carbonate In water at 85℃; for 2h;
Stage #2: With hydrogenchloride In water for 1h;
80%
3-hydroxybutanenitrile
4368-06-3

3-hydroxybutanenitrile

5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

Conditions
ConditionsYield
Stage #1: 3-hydroxybutanenitrile With hydroxylamine hydrochloride; potassium carbonate In water at 20 - 60℃; for 3h;
Stage #2: With iron(III) chloride In toluene Reagent/catalyst; Temperature; Reflux;
77%
2-(5-methyl-1,2-oxazol-3-yl)-1H-isoindole-1,3(2H)-dione
91377-59-2

2-(5-methyl-1,2-oxazol-3-yl)-1H-isoindole-1,3(2H)-dione

5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

Conditions
ConditionsYield
With hydrazine hydrate In ethanol for 3h; Heating;75.1%
cyclohexa-1,3-diene
1165952-91-9

cyclohexa-1,3-diene

A

5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

exo-3-(5-methylisoxazol-3-yl)-2λ4-thia-3-azabicyclo[2.2.2]oct-5-ene 2 oxide

exo-3-(5-methylisoxazol-3-yl)-2λ4-thia-3-azabicyclo[2.2.2]oct-5-ene 2 oxide

(1RS,2SR,4SR)-(2-oxo-2λ4-thia-3-azabicyclo[2.2.2]oct-5-en-3-yl)phosphonic acid diphenyl ester

(1RS,2SR,4SR)-(2-oxo-2λ4-thia-3-azabicyclo[2.2.2]oct-5-en-3-yl)phosphonic acid diphenyl ester

Conditions
ConditionsYield
In tetrahydrofuran at 20℃; for 22h; hetero-Diels-Alder reaction;A n/a
B n/a
C 64%
(5-methyl-isoxazol-3-yl)-carbamic acid benzyl ester
100143-11-1

(5-methyl-isoxazol-3-yl)-carbamic acid benzyl ester

5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

Conditions
ConditionsYield
With sodium hydroxide
(5-methyl-isoxazol-3-yl)-carbamic acid ethyl ester
92087-97-3

(5-methyl-isoxazol-3-yl)-carbamic acid ethyl ester

5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

Conditions
ConditionsYield
With sodium hydroxide
but-2-enenitrile
4786-20-3

but-2-enenitrile

5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

Conditions
ConditionsYield
(i) Br2, MeOH, (ii) aq. NaOH, NH2CONHOH; Multistep reaction;
(Z)-4-(5-Methyl-isoxazol-3-ylamino)-pent-3-en-2-one
106124-31-6

(Z)-4-(5-Methyl-isoxazol-3-ylamino)-pent-3-en-2-one

5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

Conditions
ConditionsYield
With sodium ethanolate In ethanol for 3h; Heating; Yield given;
sulfamethoxazole
723-46-6

sulfamethoxazole

A

5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

B

C10H10ClN3O3S

C10H10ClN3O3S

C

4-amino-3-chloro-N-(5-methyl-isoxazol-3-yl)-benzenesulphonamide

4-amino-3-chloro-N-(5-methyl-isoxazol-3-yl)-benzenesulphonamide

Conditions
ConditionsYield
With sodium hypochlorite; borate buffer at 25℃; pH=9; Kinetics; Further Variations:; pH-values; Reagents; Solvents;
sulfamethoxazole
723-46-6

sulfamethoxazole

A

5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

B

C10H13N3O4S

C10H13N3O4S

C

C10H13N3O5S

C10H13N3O5S

D

N-(5-methyl-isoxazol-3-yl)-4-nitro-benzenesulfonamide
29699-89-6

N-(5-methyl-isoxazol-3-yl)-4-nitro-benzenesulfonamide

Conditions
ConditionsYield
With hydrogenchloride; water; sodium chloride; sodium hydroxide pH=9.5; Catalytic behavior; Mechanism; Kinetics; pH-value; Reagent/catalyst; Inert atmosphere;
sulfamethoxazole
723-46-6

sulfamethoxazole

A

5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

B

benzenesulfonamide
98-10-2

benzenesulfonamide

C

1,2,4-Trihydroxybenzene
533-73-3

1,2,4-Trihydroxybenzene

D

N-((4-aminophenyl)sulfonyl)carbamimidic acid
547-44-4

N-((4-aminophenyl)sulfonyl)carbamimidic acid

E

3-hydroxybenzenesulfonamide
20759-40-4

3-hydroxybenzenesulfonamide

F

4-amino-N-(4-hydroxy-5-methylisoxazol-3-yl)benzenesulfonamide

4-amino-N-(4-hydroxy-5-methylisoxazol-3-yl)benzenesulfonamide

G

N-(4,5-dihydroxy-5-methyl-4,5-dihydroisoxazol-3-yl)-4-hydroxybenzenesulfonamide

N-(4,5-dihydroxy-5-methyl-4,5-dihydroisoxazol-3-yl)-4-hydroxybenzenesulfonamide

H

N-(4,5-dihydroxy-5-methyl-4,5-dihydroisoxazol-3-yl)benzenesulfonamide

N-(4,5-dihydroxy-5-methyl-4,5-dihydroisoxazol-3-yl)benzenesulfonamide

I

(Z)-N-((2-oxopropylidene)carbamoyl)methanesulfonamide

(Z)-N-((2-oxopropylidene)carbamoyl)methanesulfonamide

J

3,4-dihydroxy-N-(5-methylisoxazol-3-yl)benzenesulfonamide

3,4-dihydroxy-N-(5-methylisoxazol-3-yl)benzenesulfonamide

K

3,4-dihydroxy-N-(4-hydroxy-5-methylisoxazol-3-yl)benzenesulfonamide

3,4-dihydroxy-N-(4-hydroxy-5-methylisoxazol-3-yl)benzenesulfonamide

L

4-amino-3-hydroxy-N- (5-methylisoxazol-3-yl)benzenesulfonamide

4-amino-3-hydroxy-N- (5-methylisoxazol-3-yl)benzenesulfonamide

M

4-amino-3-hydroxy-N-(4-hydroxy-5-methylisoxazol-3-yl)benzenesulfonamide

4-amino-3-hydroxy-N-(4-hydroxy-5-methylisoxazol-3-yl)benzenesulfonamide

N

2-oxo-N-(phenylsulfonyl)acetimidamide

2-oxo-N-(phenylsulfonyl)acetimidamide

O

4-hydroxy-N-(5-methyl-3-isoxazolyl)benzenesulphonamide
141233-20-7

4-hydroxy-N-(5-methyl-3-isoxazolyl)benzenesulphonamide

P

N-(5-methyl-isoxazol-3-yl)-4-nitro-benzenesulfonamide
29699-89-6

N-(5-methyl-isoxazol-3-yl)-4-nitro-benzenesulfonamide

Q

phenol
108-95-2

phenol

Conditions
ConditionsYield
With AgBr-BaMoO4 composite photocatalyst In water for 1.25h; Kinetics; Reagent/catalyst; UV-irradiation;
sulfamethoxazole
723-46-6

sulfamethoxazole

A

5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

B

5-methyl-3-nitrosoisoxazole
947619-95-6

5-methyl-3-nitrosoisoxazole

C

4-amino-3-hydroxy-N- (5-methylisoxazol-3-yl)benzenesulfonamide

4-amino-3-hydroxy-N- (5-methylisoxazol-3-yl)benzenesulfonamide

D

4-amino-3-hydroxy-N-(4-hydroxy-5-methylisoxazol-3-yl)benzenesulfonamide

4-amino-3-hydroxy-N-(4-hydroxy-5-methylisoxazol-3-yl)benzenesulfonamide

E

C4H8N2O

C4H8N2O

Conditions
ConditionsYield
With sodium sulfate In water pH=7; Kinetics; pH-value; Reagent/catalyst; Electrochemical reaction;
N1-acetylsulfamethoxazole
18607-98-2

N1-acetylsulfamethoxazole

A

5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

B

5-methyl-3-nitrosoisoxazole
947619-95-6

5-methyl-3-nitrosoisoxazole

C

N-acetylsulfanilic acid
121-62-0

N-acetylsulfanilic acid

D

nitroso derivative of sulfamethoxazole
131549-85-4

nitroso derivative of sulfamethoxazole

E

Benzenesulfinic acid
618-41-7

Benzenesulfinic acid

F

N-(5-methyl-isoxazol-3-yl)-4-nitro-benzenesulfonamide
29699-89-6

N-(5-methyl-isoxazol-3-yl)-4-nitro-benzenesulfonamide

Conditions
ConditionsYield
With sodium sulfate In water pH=7; Kinetics; pH-value; Reagent/catalyst; Electrochemical reaction;
sulfamethoxazole
723-46-6

sulfamethoxazole

A

5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

B

3-nitro-5-methylisoxazole
75079-82-2

3-nitro-5-methylisoxazole

C

5-methyl-3-nitrosoisoxazole
947619-95-6

5-methyl-3-nitrosoisoxazole

D

4-amino-3-hydroxy-N- (5-methylisoxazol-3-yl)benzenesulfonamide

4-amino-3-hydroxy-N- (5-methylisoxazol-3-yl)benzenesulfonamide

Conditions
ConditionsYield
With iron(III) sulfate; sodium hydrogensulfite at 25℃; pH=4; Kinetics; pH-value;
sulfamethoxazole
723-46-6

sulfamethoxazole

A

5-methylisoxazole
5765-44-6

5-methylisoxazole

B

5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

C

1-hydroxy-2-aminobenzene-5-sulfonic acid
2592-14-5

1-hydroxy-2-aminobenzene-5-sulfonic acid

D

C9H8N2O4S

C9H8N2O4S

E

4-hydroxy-N-(5-methyl-3-isoxazolyl)benzenesulphonamide
141233-20-7

4-hydroxy-N-(5-methyl-3-isoxazolyl)benzenesulphonamide

F

(5-methyl-1,2-oxazol-3-yl)sulfamic acid

(5-methyl-1,2-oxazol-3-yl)sulfamic acid

G

N-(5-methyl-isoxazol-3-yl)-4-nitro-benzenesulfonamide
29699-89-6

N-(5-methyl-isoxazol-3-yl)-4-nitro-benzenesulfonamide

Conditions
ConditionsYield
Stage #1: sulfamethoxazole With 0D/1D 50 wt.% AgI/MoO3 Z-scheme heterojunction composite In water for 0.5h; Darkness; Sonication;
Stage #2: In water pH=3.92; Kinetics; Catalytic behavior; Reagent/catalyst; Irradiation;
5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

5-chlorosalicyclaldehyde
635-93-8

5-chlorosalicyclaldehyde

3-(2-hydroxy-8-chlorobenzylideneamino)-5-methylisoxazole
88812-64-0

3-(2-hydroxy-8-chlorobenzylideneamino)-5-methylisoxazole

Conditions
ConditionsYield
Reflux;100%
In ethanol for 2h; Reflux;88%
In ethanol Heating;
5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

5-bromosalicyclaldehyde
1761-61-1

5-bromosalicyclaldehyde

4-bromo-2-[(5-methyl-3-isoxazolyl)imino]methylphenol
88812-68-4

4-bromo-2-[(5-methyl-3-isoxazolyl)imino]methylphenol

Conditions
ConditionsYield
Reflux;100%
In ethanol for 2h; Reflux;95%
In ethanol Heating;
5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

piperonal
120-57-0

piperonal

[1-Benzo[1,3]dioxol-5-yl-meth-(E)-ylidene]-(5-methyl-isoxazol-3-yl)-amine
88812-71-9

[1-Benzo[1,3]dioxol-5-yl-meth-(E)-ylidene]-(5-methyl-isoxazol-3-yl)-amine

Conditions
ConditionsYield
Heating;100%
In ethanol; chloroform
5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

4-methyl-benzaldehyde
104-87-0

4-methyl-benzaldehyde

(5-Methyl-isoxazol-3-yl)-[1-p-tolyl-meth-(E)-ylidene]-amine
112633-38-2

(5-Methyl-isoxazol-3-yl)-[1-p-tolyl-meth-(E)-ylidene]-amine

Conditions
ConditionsYield
Heating;100%
With 1-methylimidazolium tetrafluoroborate at 30℃; for 0.25h;
In ethanol; chloroform
5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

4-chlorobenzaldehyde
104-88-1

4-chlorobenzaldehyde

N-(4-chlorobenzylidene)-5-methylisoxazol-3-amine
88812-63-9

N-(4-chlorobenzylidene)-5-methylisoxazol-3-amine

Conditions
ConditionsYield
Heating;100%
With 1-methylimidazolium tetrafluoroborate at 30℃;
In ethanol; chloroform
In ethanol Reflux;
5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

2-chloro-benzaldehyde
89-98-5

2-chloro-benzaldehyde

[1-(2-Chloro-phenyl)-meth-(E)-ylidene]-(5-methyl-isoxazol-3-yl)-amine
112633-41-7

[1-(2-Chloro-phenyl)-meth-(E)-ylidene]-(5-methyl-isoxazol-3-yl)-amine

Conditions
ConditionsYield
Heating;100%
With trimethylsilyl acetate; zinc(II) chloride In N,N-dimethyl-formamide at 100℃; for 8h;
5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

3-nitro-benzaldehyde
99-61-6

3-nitro-benzaldehyde

(5-Methyl-isoxazol-3-yl)-[1-(3-nitro-phenyl)-meth-(E)-ylidene]-amine
88812-66-2

(5-Methyl-isoxazol-3-yl)-[1-(3-nitro-phenyl)-meth-(E)-ylidene]-amine

Conditions
ConditionsYield
Heating;100%
In ethanol; chloroform
5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

4-nitrobenzaldehdye
555-16-8

4-nitrobenzaldehdye

(5-Methyl-isoxazol-3-yl)-[1-(4-nitro-phenyl)-meth-(Z)-ylidene]-amine
112633-39-3

(5-Methyl-isoxazol-3-yl)-[1-(4-nitro-phenyl)-meth-(Z)-ylidene]-amine

Conditions
ConditionsYield
Heating;100%
In ethanol; chloroform
With acetic acid In 1,2-dichloro-ethane at 60℃; for 1.5h;
With tert-butylisonitrile; phenylpropyolic acid In methanol at 20℃; for 24h;
5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

benzaldehyde
100-52-7

benzaldehyde

N-benzylidene-5-methylisoxazol-3-amine
112633-37-1

N-benzylidene-5-methylisoxazol-3-amine

Conditions
ConditionsYield
Heating;100%
With 1-methylimidazolium tetrafluoroborate at 30℃; for 0.25h;
In ethanol; chloroform
With acetic acid In 1,2-dichloro-ethane at 60℃; for 1.5h;
With magnesium sulfate In ethanol at 20℃;
5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

4-methoxy-benzaldehyde
123-11-5

4-methoxy-benzaldehyde

[1-(4-Methoxy-phenyl)-meth-(E)-ylidene]-(5-methyl-isoxazol-3-yl)-amine
88812-69-5

[1-(4-Methoxy-phenyl)-meth-(E)-ylidene]-(5-methyl-isoxazol-3-yl)-amine

Conditions
ConditionsYield
Heating;100%
With piperidine In ethanol for 0.166667h; Reflux;76%
With 1-methylimidazolium tetrafluoroborate at 30℃;
In ethanol; chloroform
5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

2,4-dichlorobenzaldeyhde
874-42-0

2,4-dichlorobenzaldeyhde

[1-(2,4-Dichloro-phenyl)-meth-(E)-ylidene]-(5-methyl-isoxazol-3-yl)-amine
112661-91-3

[1-(2,4-Dichloro-phenyl)-meth-(E)-ylidene]-(5-methyl-isoxazol-3-yl)-amine

Conditions
ConditionsYield
Heating;100%
In ethanol; chloroform
5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

2-hydroxy-5-methoxybenzaldehyde
672-13-9

2-hydroxy-5-methoxybenzaldehyde

4-methoxy-2-[(5-methyl-3-isoxazolyl)imino]methylphenol
415715-07-0

4-methoxy-2-[(5-methyl-3-isoxazolyl)imino]methylphenol

Conditions
ConditionsYield
Reflux;100%
In ethanol for 2h; Reflux;90%
5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

2-hydroxy-5-methylbenzaldehyde
613-84-3

2-hydroxy-5-methylbenzaldehyde

4-methyl-2-[(5-methyl-3-isoxazolyl)imino]methylphenol
326878-69-7

4-methyl-2-[(5-methyl-3-isoxazolyl)imino]methylphenol

Conditions
ConditionsYield
Reflux;100%
In ethanol for 2h; Reflux;90%
5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

salicylaldehyde
90-02-8

salicylaldehyde

2-((5-methylisoxazol-3-ylimino)methyl)phenol
112633-43-9

2-((5-methylisoxazol-3-ylimino)methyl)phenol

Conditions
ConditionsYield
Reflux;100%
In ethanol for 2h; Reflux;95%
In methanol Reflux;82%
5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

3,5-Dibromosalicylaldehyde
90-59-5

3,5-Dibromosalicylaldehyde

C11H8Br2N2O2
116808-16-3

C11H8Br2N2O2

Conditions
ConditionsYield
Reflux;100%
5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

3,5-dichlorosalicyclaldehyde
90-60-8

3,5-dichlorosalicyclaldehyde

C11H8Cl2N2O2
88812-65-1

C11H8Cl2N2O2

Conditions
ConditionsYield
Reflux;100%
5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

diisopropyl-carbodiimide
693-13-0

diisopropyl-carbodiimide

1,3-diisopropyl-2-(5-methylisoxazol-3-yl)guanidine

1,3-diisopropyl-2-(5-methylisoxazol-3-yl)guanidine

Conditions
ConditionsYield
[{Me2Si(C5Me4)(NPh)}Y(CH2SiMe3)(thf)2] In tetrahydrofuran at 20℃; for 1h;99%
5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

mercaptoacetic acid
68-11-1

mercaptoacetic acid

4-cyanobenzaldehyde
105-07-7

4-cyanobenzaldehyde

4-(3-(5-methylisoxazol-3-yl)-4-oxothiazolidin-2-yl)benzonitrile
1610829-08-7

4-(3-(5-methylisoxazol-3-yl)-4-oxothiazolidin-2-yl)benzonitrile

Conditions
ConditionsYield
In toluene Reflux; Dean-Stark;98.7%
5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

2,7-Dihydroxynaphthalene
582-17-2

2,7-Dihydroxynaphthalene

4-fluorobenzaldehyde
459-57-4

4-fluorobenzaldehyde

C21H17FN2O3
1380601-72-8

C21H17FN2O3

Conditions
ConditionsYield
at 80℃; for 0.5h; Neat (no solvent);98%
5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

(1,1,1-trifluoro-2-(trifluoromethyl)-but-2-yl)isocyanate
312932-31-3

(1,1,1-trifluoro-2-(trifluoromethyl)-but-2-yl)isocyanate

1-[1,1-bis(trifluoromethyl)propyl]-3-(5-methylisoxazol-3-yl)urea
355829-46-8

1-[1,1-bis(trifluoromethyl)propyl]-3-(5-methylisoxazol-3-yl)urea

Conditions
ConditionsYield
In diethyl ether at 20℃; for 4h;98%
5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

4-Nitrobenzenesulfonyl chloride
98-74-8

4-Nitrobenzenesulfonyl chloride

N-(5-methyl-isoxazol-3-yl)-4-nitro-benzenesulfonamide
29699-89-6

N-(5-methyl-isoxazol-3-yl)-4-nitro-benzenesulfonamide

Conditions
ConditionsYield
With pyridine at 20℃; for 5h;97%
95%
With pyridine at 0℃; for 2h; Inert atmosphere;90%
5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

C12H12ClN3O
1338361-28-6

C12H12ClN3O

1-(3,4-dimethylphenyl)-5-methyl-N-(5-methylisoxazol-3-yl)-1H-1,2,3-triazole-4-carboxamide
915910-20-2

1-(3,4-dimethylphenyl)-5-methyl-N-(5-methylisoxazol-3-yl)-1H-1,2,3-triazole-4-carboxamide

Conditions
ConditionsYield
With triethylamine In acetonitrile at 70℃;97%
5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

bromobenzene
108-86-1

bromobenzene

3-anilino-5-methylisoxazole
71854-24-5

3-anilino-5-methylisoxazole

Conditions
ConditionsYield
With [2-(di-tert-butylphosphino)-2′,4′,6′-triisopropyl-1,1′-biphenyl][2-((2-aminoethyl)phenyl)]palladium(II) chloride; sodium t-butanolate; tert-butyl XPhos In tert-butyl alcohol at 20℃; for 2h; Inert atmosphere;97%
5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

2,7-Dihydroxynaphthalene
582-17-2

2,7-Dihydroxynaphthalene

4-nitrobenzaldehdye
555-16-8

4-nitrobenzaldehdye

1-[(5-methylisoxazol-3-ylamino)(4-nitrophenyl)methyl]naphthalene-2,7-diol
1380601-75-1

1-[(5-methylisoxazol-3-ylamino)(4-nitrophenyl)methyl]naphthalene-2,7-diol

Conditions
ConditionsYield
at 80℃; for 0.5h; Neat (no solvent);97%
5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

1H-indol-2-ylcarboxaldehyde
19005-93-7

1H-indol-2-ylcarboxaldehyde

N-((1H-indol-2-yl)methylene)-5-methylisoxazol-3-amine

N-((1H-indol-2-yl)methylene)-5-methylisoxazol-3-amine

Conditions
ConditionsYield
With acetic acid In methanol at 30℃; for 0.2h; Temperature; Sonication;97%
5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

2,4,6-trimethoxybenzaldehyde
830-79-5

2,4,6-trimethoxybenzaldehyde

N-(2,4,6-trimethoxybenzylidene)-5-methylisoxazol-3-amine

N-(2,4,6-trimethoxybenzylidene)-5-methylisoxazol-3-amine

Conditions
ConditionsYield
With acetic acid In methanol at 30℃; for 0.2h; Temperature; Sonication;97%
5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

2,6-difluorobenzaldehyde
437-81-0

2,6-difluorobenzaldehyde

mercaptoacetic acid
68-11-1

mercaptoacetic acid

2-(2,6-difluorophenyl)-3-(5-methylisoxazol-3-yl)thiazolidin-4-one
1350308-04-1

2-(2,6-difluorophenyl)-3-(5-methylisoxazol-3-yl)thiazolidin-4-one

Conditions
ConditionsYield
In toluene Reflux;96.7%
5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

2,6-dichlorobenzaldehyde
83-38-5

2,6-dichlorobenzaldehyde

mercaptoacetic acid
68-11-1

mercaptoacetic acid

2-(2,6-dichlorophenyl)-3-(5-methylisoxazol-3-yl)thiazolidin-4-one
1350308-03-0

2-(2,6-dichlorophenyl)-3-(5-methylisoxazol-3-yl)thiazolidin-4-one

Conditions
ConditionsYield
In toluene Reflux;96.5%
5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

Triethyl orthoacetate
78-39-7

Triethyl orthoacetate

ethyl N-(5-methylisoxazol-3-yl)acetimidate

ethyl N-(5-methylisoxazol-3-yl)acetimidate

Conditions
ConditionsYield
for 1.5h; Heating;96%
5-methylisoxazol-3-ylamine
1072-67-9

5-methylisoxazol-3-ylamine

ethyl (ethoxymethylene)cyanoacetate
94-05-3

ethyl (ethoxymethylene)cyanoacetate

ethyl 2-cyano-3-(5-methylisoxazol-3-ylamino)acrylate
219619-78-0

ethyl 2-cyano-3-(5-methylisoxazol-3-ylamino)acrylate

Conditions
ConditionsYield
In ethanol for 1.5h; Reflux;96%

3-Amino-5-Methylisoxazole Chemical Properties


Molecular Formula:C4H6N2O
Molar mass:98.10324g/mol
Structure of 3-Amino-5-methylisoxazole(1072-67-9):
                                
Synonyms of 3-Amino-5-methylisoxazole(1072-67-9):3-Isoxazolamine, 5-methyl-;Isoxazole, 3-amino-5-methyl-;5-Methyl-3-aminoisoxazole;3-Methyl-5-aminoisoxazole;5-methylisoxazol-3-amine;5-Methyl-3-isoxazolamine
Density:1.167 g/cm3                 
Flash Point:96.5 °C      
Boiling Point:235.9 °C at 760 mmHg 
Index of Refraction:1.524                      
Vapour Pressure:0.0487 mmHg at 25°C               
Melting point:59-63°C
Solubility:Soluble in alcohol, ether, vapor volatile with water
Water solubility:soluble
Appearance:White crystals
storage temp:Refrigerator

3-Amino-5-Methylisoxazole Uses

3-Amino-5-methylisoxazole(1072-67-9) is pharmaceutical intermediates,and can be used for the production of sulfonamide.

3-Amino-5-Methylisoxazole Production

3-Amino-5-methylisoxazole(1072-67-9) can be derived from the degradation of 5 - methylisoxazole -3 - carboxamide.

3-Amino-5-Methylisoxazole Toxicity Data With Reference

1.Oral, mus: LD50 = 3060-4060 mg/kg (24H) Oral, mus: LD50 = 2409-3271 mg/kg (10D)
2.Carcinogenicity:3-Amino-5-methylisoxazole(1072-67-9)- Not listed as a carcinogen by  NTP, IARC,ACGIH, or CA Prop 65.

3-Amino-5-Methylisoxazole Safety Profile

Hazard Codes:Xi-F,Xi,F,Xn
Risk Statements:
5:  Heating may cause an explosion
10:  Flammable
11:  Highly Flammable
20:  Harmful by inhalation
21:  Harmful in contact with skin
22:  Harmful if swallowed 
36:  Irritating to the eyes
37:  Irritating to the respiratory system
38:  Irritating to the skin
Safety Statements:
16:  Keep away from sources of ignition - No smoking
22:  Do not breathe dust 
24:  Avoid contact with skin
25:  Avoid contact with eyes
26:  In case of contact with eyes, rinse immediately with plenty of water and seek medical advice 
36:  Wear suitable protective clothing 
37:  Wear suitable gloves
39:  Wear eye/face protection
47:  Keep at temperature not exceeding ... E C (to be specified by the manufacturer)

3-Amino-5-Methylisoxazole Specification

Stability and Reactivity of 3-Amino-5-methylisoxazole(1072-67-9):
Conditions to Avoid:Incompatible materials, temperatures above 65°C, ignition sources,light. 
Chemical Stability:Stable under normal pressures and temperatures. 
Incompatibilities with Other Materials:Strong oxidizing agents.
Hazardous Decomposition Products: Nitrogen oxides, carbon monoxide, carbon dioxide.
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