Product Name

  • Name

    2-Aminothiazole

  • EINECS 202-511-6
  • CAS No. 96-50-4
  • Article Data81
  • CAS DataBase
  • Density 1.346 g/cm3
  • Solubility Slightly soluble in cold water, ethanol, soluble in water, dilute inorganic acid
  • Melting Point 91-93 °C(lit.)
  • Formula C3H4N2S
  • Boiling Point 216.383 °C at 760 mmHg
  • Molecular Weight 100.144
  • Flash Point 84.666 °C
  • Transport Information UN 2811
  • Appearance Light brown crystals or brown granular solid.
  • Safety 26-36/37-39
  • Risk Codes 36/37-20/21/22
  • Molecular Structure Molecular Structure of 96-50-4 (2-Aminothiazole)
  • Hazard Symbols HarmfulXn,IrritantXi
  • Synonyms Thiazole, 2-amino-;Aminothiazole;2-Thiazolamine;2-Thiazolylamine;4-Thiazolin-2-onimine;AI3-14917;Abadol;Abadole;Aminothiazol;Aminothiazolum;Basedol;CCRIS 1279;CP 1585;NSC 1900;RP 2921;UNII-5K8WKN668K;USAF EK-P-5501;
  • PSA 67.15000
  • LogP 1.30650

Synthetic route

2-azido-1,3-thiazole
58822-97-2

2-azido-1,3-thiazole

2-thiazolylamine
96-50-4

2-thiazolylamine

Conditions
ConditionsYield
With iron(III) oxide; hydrazine hydrate In water at 120℃; for 2h; Inert atmosphere;99%
With D-glucose; potassium hydroxide In water at 85℃; for 0.25h; Green chemistry; chemoselective reaction;97%
acetaldehyde
75-07-0

acetaldehyde

thiourea
17356-08-0

thiourea

2-thiazolylamine
96-50-4

2-thiazolylamine

Conditions
ConditionsYield
Stage #1: acetaldehyde With 1,3-dichloro-5,5-dimethylhydantoin; iron oxide In methanol at 65℃; for 1h; Green chemistry;
Stage #2: thiourea In methanol for 1h; Catalytic behavior; Green chemistry;
98%
With montmorillonite K10 Clay; iodine In dimethyl sulfoxide at 80℃; for 2h; Green chemistry;98%
With iodine In dimethyl sulfoxide at 80℃; for 1h; Green chemistry;95%
2-bromo-1,3-thiazole
3034-53-5

2-bromo-1,3-thiazole

2-thiazolylamine
96-50-4

2-thiazolylamine

Conditions
ConditionsYield
With copper(I) oxide; ammonia at 80℃; for 16h;94%
With copper acetylacetonate; potassium phosphate; ammonia In N,N-dimethyl-formamide at 25℃; for 48h; Glovebox; Autoclave; chemoselective reaction;82 %Chromat.
1,2-dichloro-2-ethoxyethane
623-46-1

1,2-dichloro-2-ethoxyethane

thiourea
17356-08-0

thiourea

2-thiazolylamine
96-50-4

2-thiazolylamine

Conditions
ConditionsYield
Hantzsch thiazole synthesis;90%
90%
With water
2-nitrothiazole
1606-76-4

2-nitrothiazole

2-thiazolylamine
96-50-4

2-thiazolylamine

Conditions
ConditionsYield
With triethylamine In water at 80℃; for 8h; Inert atmosphere; Green chemistry; chemoselective reaction;90%
2-acetamidothiazole
2719-23-5

2-acetamidothiazole

2-thiazolylamine
96-50-4

2-thiazolylamine

Conditions
ConditionsYield
Stage #1: 2-acetamidothiazole With Schwartz's reagent In tetrahydrofuran at 20℃; for 0.05h; Inert atmosphere;
Stage #2: With water In tetrahydrofuran Inert atmosphere;
88%
2-chloroethanal
107-20-0

2-chloroethanal

thiourea
17356-08-0

thiourea

2-thiazolylamine
96-50-4

2-thiazolylamine

Conditions
ConditionsYield
In toluene at 80℃; for 2h; Temperature;85.9%
In water; toluene at 80℃; for 3h;78%
In toluene at 80℃; for 2h; Yield given;
In water at 20℃;
thiourea
17356-08-0

thiourea

acrylic acid methyl ester
292638-85-8

acrylic acid methyl ester

2-thiazolylamine
96-50-4

2-thiazolylamine

Conditions
ConditionsYield
With bromine In water for 0.666667h; Heating;80%
3-methoxy-2-propenenitrile
60838-50-8

3-methoxy-2-propenenitrile

sodium acetate
127-09-3

sodium acetate

thiourea
17356-08-0

thiourea

2-thiazolylamine
96-50-4

2-thiazolylamine

Conditions
ConditionsYield
Stage #1: 3-methoxy-2-propenenitrile With sodium hydroxide; bromine In water; acetonitrile at 5 - 10℃; for 1.33333h;
Stage #2: thiourea With sodium acetate In water; acetonitrile at 10 - 15℃; for 2.25h;
Stage #3: sodium acetate With sodium hydroxide more than 3 stages;
75%
mercaptoacetaldehyde
4124-63-4

mercaptoacetaldehyde

carbamimidothioic acid methyl ester
2986-19-8

carbamimidothioic acid methyl ester

2-thiazolylamine
96-50-4

2-thiazolylamine

Conditions
ConditionsYield
In water at 20℃; for 16h; pH=7;72%
CYANAMID
420-04-2

CYANAMID

mercaptoacetaldehyde
4124-63-4

mercaptoacetaldehyde

2-thiazolylamine
96-50-4

2-thiazolylamine

Conditions
ConditionsYield
pH=7; aq. phosphate buffer;60%
Stage #1: CYANAMID With methylthiol
Stage #2: mercaptoacetaldehyde In water at 20℃; for 16h; pH=7;
2-(2,5-dimethyl-1H-pyrrol-1-yl)-1,3-thiazole
28142-85-0

2-(2,5-dimethyl-1H-pyrrol-1-yl)-1,3-thiazole

2-thiazolylamine
96-50-4

2-thiazolylamine

Conditions
ConditionsYield
With hydrogenchloride In ethanol at 120℃; for 0.5h; Microwave irradiation;52%
chloroacetaldehyde dimethyl acetal
97-97-2

chloroacetaldehyde dimethyl acetal

thiourea
17356-08-0

thiourea

2-thiazolylamine
96-50-4

2-thiazolylamine

Conditions
ConditionsYield
With toluene-4-sulfonic acid In water Heating;37%
Sulfathiazole
72-14-0

Sulfathiazole

A

2-thiazolylamine
96-50-4

2-thiazolylamine

B

aniline
62-53-3

aniline

Conditions
ConditionsYield
In diethyl ether Product distribution; Mechanism; Ambient temperature; Irradiation;A n/a
B 23%
In methanol for 32h; Product distribution; Mechanism; Irradiation; λ=254 nm; other time, other λ;A n/a
B 23.3%
2-chloromethyl-1,3-dioxolane
2568-30-1

2-chloromethyl-1,3-dioxolane

thiourea
17356-08-0

thiourea

2-thiazolylamine
96-50-4

2-thiazolylamine

Conditions
ConditionsYield
With hydrogenchloride; acetone
1,2-dichloroethyl acetate
10140-87-1

1,2-dichloroethyl acetate

potassium thioacyanate
333-20-0

potassium thioacyanate

2-thiazolylamine
96-50-4

2-thiazolylamine

Conditions
ConditionsYield
With ethanol Erwaermen des Reaktionsprodukts mit konz. wss. NH3;
benzene
5664-49-3

benzene

A

2-thiazolylamine
96-50-4

2-thiazolylamine

B

1-phenyl-N-thiazol-2-yl-metanimine
13243-76-0

1-phenyl-N-thiazol-2-yl-metanimine

Conditions
ConditionsYield
Beim Erhitzen;
N,N'-bis-thiazol-2-yl-hydrazine; dihydrochloride

N,N'-bis-thiazol-2-yl-hydrazine; dihydrochloride

2-thiazolylamine
96-50-4

2-thiazolylamine

Conditions
ConditionsYield
With iron; acetic acid
1,2-dichloroethyl acetate
10140-87-1

1,2-dichloroethyl acetate

thiourea
17356-08-0

thiourea

2-thiazolylamine
96-50-4

2-thiazolylamine

Conditions
ConditionsYield
With water
With methanol
ethanol
64-17-5

ethanol

thiourea
17356-08-0

thiourea

2-thiazolylamine
96-50-4

2-thiazolylamine

Conditions
ConditionsYield
With chlorine
bis-(1,2-dichloro-ethyl) ether
7166-44-1

bis-(1,2-dichloro-ethyl) ether

thiourea
17356-08-0

thiourea

2-thiazolylamine
96-50-4

2-thiazolylamine

Conditions
ConditionsYield
With water
2-chloral-1-methoxyethyl acetate
40916-19-6

2-chloral-1-methoxyethyl acetate

thiourea
17356-08-0

thiourea

2-thiazolylamine
96-50-4

2-thiazolylamine

Conditions
ConditionsYield
With water
monochloroacetaldehyde hydrate
15873-56-0

monochloroacetaldehyde hydrate

thiourea
17356-08-0

thiourea

2-thiazolylamine
96-50-4

2-thiazolylamine

thiourea
17356-08-0

thiourea

chloroacetaldehyde diethyl acetal
621-62-5

chloroacetaldehyde diethyl acetal

2-thiazolylamine
96-50-4

2-thiazolylamine

Conditions
ConditionsYield
With water
With (aq. acid solution)
With water
thiourea
17356-08-0

thiourea

paracetaldehyde
123-63-7

paracetaldehyde

2-thiazolylamine
96-50-4

2-thiazolylamine

Conditions
ConditionsYield
With sulfuryl dichloride
With water; bromine
thiourea
17356-08-0

thiourea

Bromoacetaldehyde diethyl acetal
2032-35-1

Bromoacetaldehyde diethyl acetal

2-thiazolylamine
96-50-4

2-thiazolylamine

Conditions
ConditionsYield
With hydrogenchloride
2-aminothiazole-5-carboxylic acid
40283-46-3

2-aminothiazole-5-carboxylic acid

2-thiazolylamine
96-50-4

2-thiazolylamine

Conditions
ConditionsYield
In water at 60℃; Rate constant; Mechanism; pH's from -1.1 to 5.67;
salicylidene-2-aminothiazole
21151-43-9

salicylidene-2-aminothiazole

A

2-thiazolylamine
96-50-4

2-thiazolylamine

B

salicylaldehyde
90-02-8

salicylaldehyde

Conditions
ConditionsYield
With water; cetyltrimethylammonim bromide; potassium bromide In methanol at 35℃; Rate constant; Product distribution; Mechanism; other N-salicylidene deriv.; other surfactant; var. conc. of surfactants and pH values;
With sodium hydroxide In ethanol; water at 30℃; Kinetics; Rate constant; Ea;
2-(2-thiazolylimino)-3-allyl-4-thiazolidinone
114710-72-4

2-(2-thiazolylimino)-3-allyl-4-thiazolidinone

A

2-thiazolylamine
96-50-4

2-thiazolylamine

B

3-allylthiazolidine-2,4-dione
39137-27-4

3-allylthiazolidine-2,4-dione

Conditions
ConditionsYield
With hydrogenchloride In various solvent(s) for 8h; Heating;
With hydrogenchloride In various solvent(s) for 8h; Heating; other thiazolidine-2,4-diones;
C-(4-Nitro-phenyl)-N,N'-bis-thiazol-2-yl-methanediamine
107866-76-2

C-(4-Nitro-phenyl)-N,N'-bis-thiazol-2-yl-methanediamine

A

2-thiazolylamine
96-50-4

2-thiazolylamine

B

2-(4-nitrobenzylideneamino)thiazole
61863-68-1

2-(4-nitrobenzylideneamino)thiazole

Conditions
ConditionsYield
In dimethylsulfoxide-d6 at 32℃; Equilibrium constant; Rate constant;
2-thiazolylamine
96-50-4

2-thiazolylamine

di-tert-butyl dicarbonate
24424-99-5

di-tert-butyl dicarbonate

tert-butyl 1,3-thiazole-2-yl-carbamate
170961-15-6

tert-butyl 1,3-thiazole-2-yl-carbamate

Conditions
ConditionsYield
With pyridine100%
In tetrahydrofuran at 20℃; for 16h;96%
With glycerol at 20℃; for 0.5h; Green chemistry; chemoselective reaction;95%
2-thiazolylamine
96-50-4

2-thiazolylamine

potassium cyanate
590-28-3

potassium cyanate

thiazol-2-yl-urea
35107-91-6

thiazol-2-yl-urea

Conditions
ConditionsYield
With acetic acid at 20℃; for 3h;100%
2-thiazolylamine
96-50-4

2-thiazolylamine

2-(4-cyano-phenyl)-3-cyclopentyl-propionic acid

2-(4-cyano-phenyl)-3-cyclopentyl-propionic acid

oxalyl dichloride
79-37-8

oxalyl dichloride

2-(4-cyano-phenyl)-3-cyclopentyl-N-thiazol-2-yl-propionamide

2-(4-cyano-phenyl)-3-cyclopentyl-N-thiazol-2-yl-propionamide

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran; dichloromethane100%
2-thiazolylamine
96-50-4

2-thiazolylamine

3-cyclopentyl-2-(3-fluoro-4-methoxy-phenyl)-propionic acid

3-cyclopentyl-2-(3-fluoro-4-methoxy-phenyl)-propionic acid

oxalyl dichloride
79-37-8

oxalyl dichloride

3-cyclopentyl-2-(3-fluoro-4-methoxy-phenyl)-N-thiazol-2-yl-propionamide

3-cyclopentyl-2-(3-fluoro-4-methoxy-phenyl)-N-thiazol-2-yl-propionamide

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran; dichloromethane100%
2-thiazolylamine
96-50-4

2-thiazolylamine

5'-[(cyclopropylamino)carbonyl]-3'-fluoro-2'-methyl-4-[(methyloxy)carbonyl]-2-biphenylcarboxylic acid
913002-78-5

5'-[(cyclopropylamino)carbonyl]-3'-fluoro-2'-methyl-4-[(methyloxy)carbonyl]-2-biphenylcarboxylic acid

methyl 5'-[(cyclopropylamino)carbonyl]-3'-fluoro-2'-methyl-2-[(1,3-thiazol-2-ylamino)carbonyl]-4-biphenylcarboxylate
913002-79-6

methyl 5'-[(cyclopropylamino)carbonyl]-3'-fluoro-2'-methyl-2-[(1,3-thiazol-2-ylamino)carbonyl]-4-biphenylcarboxylate

Conditions
ConditionsYield
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 48h;100%
2-thiazolylamine
96-50-4

2-thiazolylamine

C17H12F2N4O2

C17H12F2N4O2

C20H14F2N6OS

C20H14F2N6OS

Conditions
ConditionsYield
With 2-(1H-9-azabenzotriazol-1-yl)-1,1,3,3-tetramethyluroniumhexafluorophosphate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; for 24h;100%
2-thiazolylamine
96-50-4

2-thiazolylamine

4-bromobenzenesulfonyl chloride
98-58-8

4-bromobenzenesulfonyl chloride

4-bromo-N-(thiazol-2-yl)benzene sulfonamide
331972-47-5

4-bromo-N-(thiazol-2-yl)benzene sulfonamide

Conditions
ConditionsYield
With pyridine at 20℃; for 19h;99%
With pyridine at 20℃; for 19h;99%
With pyridine at 20℃; for 19h;99%
With pyridine
With pyridine In dichloromethane for 24h;
2-thiazolylamine
96-50-4

2-thiazolylamine

acetaldehyde
75-07-0

acetaldehyde

etiliden-di-N-(2-aminotiazolo)

etiliden-di-N-(2-aminotiazolo)

Conditions
ConditionsYield
In aq. buffer for 24h; pH=7;99%
In ethanol Ambient temperature;
2-thiazolylamine
96-50-4

2-thiazolylamine

2-azulenylcarbaldehyde
77627-18-0

2-azulenylcarbaldehyde

N-(2-thiazolyl)-2-azulenylmethyleneimine

N-(2-thiazolyl)-2-azulenylmethyleneimine

Conditions
ConditionsYield
With benzene In ethanol at 20℃; for 1h; Heating;99%
2-thiazolylamine
96-50-4

2-thiazolylamine

4-(chlorosulfonyl)benzenesulfonyl fluoride

4-(chlorosulfonyl)benzenesulfonyl fluoride

4-(N-(thiazol-2-yl)sulfamoyl)benzene-1-sulfonyl fluoride

4-(N-(thiazol-2-yl)sulfamoyl)benzene-1-sulfonyl fluoride

Conditions
ConditionsYield
With pyridine In chloroform at 20℃; for 48h; chemoselective reaction;99%
2-thiazolylamine
96-50-4

2-thiazolylamine

1-(benzofuran-2-yl)-2-bromoethan-1-one
23489-36-3

1-(benzofuran-2-yl)-2-bromoethan-1-one

1-(benzofuran-2-yl)-2-(2-iminothiazol-3(2H)-yl)ethanone

1-(benzofuran-2-yl)-2-(2-iminothiazol-3(2H)-yl)ethanone

Conditions
ConditionsYield
In isopropyl alcohol for 1h; Reflux;98%
In chloroform for 0.5h; Heating;
2-thiazolylamine
96-50-4

2-thiazolylamine

methanetricarboxylic acid trimethyl ester
1186-73-8

methanetricarboxylic acid trimethyl ester

N6-(1,3-thiazol-2-yl)-7-hydroxy-5-oxo-5H-<1,3>thiazolo<3,2-a>pyrimidinecarboxamide

N6-(1,3-thiazol-2-yl)-7-hydroxy-5-oxo-5H-<1,3>thiazolo<3,2-a>pyrimidinecarboxamide

Conditions
ConditionsYield
at 200℃; for 0.333333h;98%
2-thiazolylamine
96-50-4

2-thiazolylamine

3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

[1-(3-Chloro-phenyl)-meth-(E)-ylidene]-thiazol-2-yl-amine

[1-(3-Chloro-phenyl)-meth-(E)-ylidene]-thiazol-2-yl-amine

Conditions
ConditionsYield
With piperidine In ethanol for 3h; Heating;98%
2-thiazolylamine
96-50-4

2-thiazolylamine

dimethyl acetylenedicarboxylate
762-42-5

dimethyl acetylenedicarboxylate

triphenylphosphine
603-35-0

triphenylphosphine

dimethyl 2-(thiazole-2-ylamino)-3-(triphenyl-λ(5)-phosphanylidene)succinate

dimethyl 2-(thiazole-2-ylamino)-3-(triphenyl-λ(5)-phosphanylidene)succinate

Conditions
ConditionsYield
In ethyl acetate at 20℃;98%
In dichloromethane at 20℃; for 2h;90%
In dichloromethane at 20℃; for 0.05h;
2-thiazolylamine
96-50-4

2-thiazolylamine

6-chloropyrazine-2-carboxylic acid chloride
148673-71-6

6-chloropyrazine-2-carboxylic acid chloride

6-chloro-pyrazine-2-carboxylic acid thiazol-2-ylamide

6-chloro-pyrazine-2-carboxylic acid thiazol-2-ylamide

Conditions
ConditionsYield
With pyridine In acetone at 20℃; for 0.5h;98%
2-thiazolylamine
96-50-4

2-thiazolylamine

1-Naphthyl isocyanate
86-84-0

1-Naphthyl isocyanate

N-1-naphthalenyl-N’-2-thiazolylurea
501008-89-5

N-1-naphthalenyl-N’-2-thiazolylurea

Conditions
ConditionsYield
In acetonitrile at 20℃;98%
2-thiazolylamine
96-50-4

2-thiazolylamine

sodium tetrachloropalladate(II)

sodium tetrachloropalladate(II)

trans-[PdCl2(2-aminothiazole)2]
61136-28-5

trans-[PdCl2(2-aminothiazole)2]

Conditions
ConditionsYield
In acetone for 3h;98%
2-thiazolylamine
96-50-4

2-thiazolylamine

4-fluorobenzoyl chloride
403-43-0

4-fluorobenzoyl chloride

4-fluoro-N-(thiazol-2-yl)benzamide

4-fluoro-N-(thiazol-2-yl)benzamide

Conditions
ConditionsYield
In pyridine at 0 - 20℃; for 15h;97%
With pyridine; sodium hydroxide
2-thiazolylamine
96-50-4

2-thiazolylamine

pivaloyl chloride
3282-30-2

pivaloyl chloride

2,2-dimethyl-N-(thiazol-2-yl)-propionamide
69212-62-0

2,2-dimethyl-N-(thiazol-2-yl)-propionamide

Conditions
ConditionsYield
With triethylamine In dichloromethane at 20℃; for 1h;97%
With triethylamine In dichloromethane at 0 - 20℃; for 1h; Inert atmosphere;72%
With triethylamine In dichloromethane at 0 - 20℃; for 1h; Inert atmosphere;72%
2-thiazolylamine
96-50-4

2-thiazolylamine

5-(1-methylsulfanyl-1-phenylmethylene)-2,2-dimethyl-1,3-dioxane-4,6-dione
112182-61-3

5-(1-methylsulfanyl-1-phenylmethylene)-2,2-dimethyl-1,3-dioxane-4,6-dione

7-Phenyl-5-oxo-5H-thiazolo<3,2-a>pyrimidine-6-carboxylic acid
123419-86-3

7-Phenyl-5-oxo-5H-thiazolo<3,2-a>pyrimidine-6-carboxylic acid

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 120 - 130℃; for 4h;97%
2-thiazolylamine
96-50-4

2-thiazolylamine

2-chloro-5-(chloromethyl)pyridine
70258-18-3

2-chloro-5-(chloromethyl)pyridine

3-(6-chloro-pyridin-3-ylmethyl)-3H-thiazol-2-ylideneamine
147670-59-5

3-(6-chloro-pyridin-3-ylmethyl)-3H-thiazol-2-ylideneamine

Conditions
ConditionsYield
In isopropyl alcohol for 40h; Heating;97%
2-thiazolylamine
96-50-4

2-thiazolylamine

6-chloro-5-tert-butylpyrazine-2-carboxylic acid chloride
879131-25-6

6-chloro-5-tert-butylpyrazine-2-carboxylic acid chloride

5-tert-butyl-6-chloro-pyrazine-2-carboxylic acid thiazol-2-ylamide

5-tert-butyl-6-chloro-pyrazine-2-carboxylic acid thiazol-2-ylamide

Conditions
ConditionsYield
With pyridine In acetone at 20℃; for 0.5h;97%
2-thiazolylamine
96-50-4

2-thiazolylamine

4-methyl-thiazole-2-carbaldehyde
13750-68-0

4-methyl-thiazole-2-carbaldehyde

(4-methyl-1,3-thiazol-2-yl-methylene)-1,3-thiazol-2-yl-amine

(4-methyl-1,3-thiazol-2-yl-methylene)-1,3-thiazol-2-yl-amine

Conditions
ConditionsYield
With 4 A molecular sieve In diethyl ether for 24h;97%
2-thiazolylamine
96-50-4

2-thiazolylamine

1-(chlorodimethylsilyl)-2,3,4,5-tetramethylcyclopenta-2,4-diene
125542-03-2

1-(chlorodimethylsilyl)-2,3,4,5-tetramethylcyclopenta-2,4-diene

(C5Me4H)SiMe2NH-2-thiazole
1000392-78-8

(C5Me4H)SiMe2NH-2-thiazole

Conditions
ConditionsYield
With triethylamine In tetrahydrofuran at 20℃; for 3h;97%
2-thiazolylamine
96-50-4

2-thiazolylamine

1,1,1,3,3,3-hexafluoro-2-isocyanato-propane
684-29-7

1,1,1,3,3,3-hexafluoro-2-isocyanato-propane

1-(thiazol-2-yl)-3-(2,2,2-trifluoro-1-(trifluoromethyl)ethyl)-urea
339355-09-8

1-(thiazol-2-yl)-3-(2,2,2-trifluoro-1-(trifluoromethyl)ethyl)-urea

Conditions
ConditionsYield
In diethyl ether at 20℃; for 4h;97%
2-thiazolylamine
96-50-4

2-thiazolylamine

(1,1,1,3,3,3-hexafluoro-2-methylprop-2-yl)isocyanate
19755-56-7

(1,1,1,3,3,3-hexafluoro-2-methylprop-2-yl)isocyanate

1-(thiazol-2-yl)-3-(2,2,2-trifluoro-1-methyl-1-(trifluoromethyl)ethyl)-urea
301320-33-2

1-(thiazol-2-yl)-3-(2,2,2-trifluoro-1-methyl-1-(trifluoromethyl)ethyl)-urea

Conditions
ConditionsYield
With triethylamine In diethyl ether at 20℃; for 4h;97%
2-thiazolylamine
96-50-4

2-thiazolylamine

4-bromophenyl isocyanate
2493-02-9

4-bromophenyl isocyanate

N-(4-bromophenyl)-N’-2-thiazolylurea
854172-62-6

N-(4-bromophenyl)-N’-2-thiazolylurea

Conditions
ConditionsYield
In acetonitrile at 20℃;97%
In dichloromethane at 20℃; for 2h;
2-thiazolylamine
96-50-4

2-thiazolylamine

2-thiazolyl-hydrazine hydrochloride

2-thiazolyl-hydrazine hydrochloride

Conditions
ConditionsYield
Stage #1: 2-thiazolylamine With hydrogenchloride; sodium nitrite In water at -10℃; for 0.166667h;
Stage #2: With tin(ll) chloride In water at -10℃; for 0.5h;
97%

2-Aminothiazole Consensus Reports

First Aid Measures:
Ingestion:Never give anything by mouth to an unconscious person. Get medical aid immediately. Do NOT induce vomiting. If conscious and alert, rinse mouth and drink 2-4 cupfuls of milk or water.
Inhalation:Remove from exposure to fresh air immediately. If not breathing, give artificial respiration. If breathing is difficult, give oxygen. Get medical aid.
Skin:Get medical aid. Flush skin with plenty of soap and water for at least 15 minutes while removing contaminated clothing and shoes. Wash clothing before reuse.
Eyes:Flush eyes with plenty of water for at least 15 minutes, occasionally lifting the upper and lower eyelids. Get medical aid.

Storage:Keep container closed when not in use. Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances. Hormones and antibiotics room. Refrigerator (approx 4 C).
Handling:Wash thoroughly after handling. Wash hands before eating. Remove contaminated clothing and wash before reuse. Use only in a well ventilated area. Minimize dust generation and accumulation. Avoid contact with eyes, skin, and clothing. Do not breathe dust, vapor, mist, or gas. Keep container tightly closed. Do not ingest or inhale.

2-Aminothiazole Specification

The 2-Aminothiazole, with the CAS registry number 96-50-4, is also known as 2-Thiazolylamine. It belongs to the product categories of Sulphur Derivatives; Thiazoles. Its EINECS number is 202-511-6. This chemical's molecular formula is C3H4N2S and molecular weight is 100.14. What's more, its systematic name is 1,3-Thiazol-2-amine. Its classification codes are: (1)Drug / Therapeutic Agent; (2)Mutation data. It should be sealed and stored in a cool and ventilated place. Moreover, it should be protected from oxides, heat and fire. This chemical is used as as pharmaceutical intermediates, and it is also used in organic synthesis.

Physical properties of 2-Aminothiazole are: (1)ACD/LogP: 0.001; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): -0.11; (4)ACD/LogD (pH 7.4): 0.00; (5)ACD/BCF (pH 5.5): 1.00; (6)ACD/BCF (pH 7.4): 1.00; (7)ACD/KOC (pH 5.5): 18.70; (8)ACD/KOC (pH 7.4): 23.76; (9)#H bond acceptors: 2; (10)#H bond donors: 2; (11)#Freely Rotating Bonds: 0; (12)Polar Surface Area: 67.15 Å2; (13)Index of Refraction: 1.645; (14)Molar Refractivity: 26.965 cm3; (15)Molar Volume: 74.417 cm3; (16)Polarizability: 10.69×10-24cm3; (17)Surface Tension: 63.92 dyne/cm; (18)Density: 1.346 g/cm3; (19)Flash Point: 84.666 °C; (20)Enthalpy of Vaporization: 45.274 kJ/mol; (21)Boiling Point: 216.383 °C at 760 mmHg; (22)Vapour Pressure: 0.14 mmHg at 25°C.

Preparation of 2-Aminothiazole: this chemical can be prepared by thiourea and 1,2-dichloro-1-ethoxy-ethane. It is a reaction of hantzsch thiazole synthesis. The yield is about 90%.

2-Aminothiazole can be prepared by thiourea and 1,2-dichloro-1-ethoxy-ethane

Uses of 2-Aminothiazole: it can be used to produce N-thiazol-2-yl-succinamic acid by heating. It will need solvent acetone with the reaction time of 6 hours. The yield is about 94%.

2-Aminothiazole can be used to produce N-thiazol-2-yl-succinamic acid by heating

When you are using this chemical, please be cautious about it as the following:
This chemical is harmful by inhalation, in contact with skin and if swallowed. It is irritating to eyes and respiratory system. In case of contact with eyes, you should rinse immediately with plenty of water and seek medical advice. When using it, you need wear suitable protective clothing, gloves and eye/face protection.

You can still convert the following datas into molecular structure:
(1)SMILES: c1csc(n1)N
(2)Std. InChI: InChI=1S/C3H4N2S/c4-3-5-1-2-6-3/h1-2H,(H2,4,5)
(3)Std. InChIKey: RAIPHJJURHTUIC-UHFFFAOYSA-N

The toxicity data is as follows:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
cat LDLo oral 120mg/kg (120mg/kg) BEHAVIORAL: TREMOR

BEHAVIORAL: COMA

LUNGS, THORAX, OR RESPIRATION: DYSPNEA
Journal of Industrial Hygiene and Toxicology. Vol. 30, Pg. 71, 1948.
guinea pig LDLo oral 120mg/kg (120mg/kg) BEHAVIORAL: TREMOR

LUNGS, THORAX, OR RESPIRATION: DYSPNEA

BEHAVIORAL: COMA
Journal of Industrial Hygiene and Toxicology. Vol. 30, Pg. 71, 1948.
mouse LD50 intraperitoneal 200mg/kg (200mg/kg)   National Technical Information Service. Vol. AD277-689,
rabbit LD50 oral 370mg/kg (370mg/kg) BEHAVIORAL: TREMOR

BEHAVIORAL: COMA

LUNGS, THORAX, OR RESPIRATION: DYSPNEA
Journal of Industrial Hygiene and Toxicology. Vol. 30, Pg. 71, 1948.
rat LD50 intravenous 570mg/kg (570mg/kg)   Naunyn-Schmiedeberg's Archiv fuer Experimentelle Pathologie und Pharmakologie. Vol. 211, Pg. 367, 1950.
rat LD50 oral 480mg/kg (480mg/kg) BEHAVIORAL: TREMOR

BEHAVIORAL: COMA

LUNGS, THORAX, OR RESPIRATION: DYSPNEA
Journal of Industrial Hygiene and Toxicology. Vol. 30, Pg. 71, 1948.

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