4-(1,3-OXAZOL-5-YL)ANILINE

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Company Name: Shaanxi Dideu Medichem Co. Ltd
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Products Intro: Product Name:4-(1,3-OXAZOL-5-YL)ANILINE
CAS:1008-95-3
Purity:99.0% Package:1KG;|25KG
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Products Intro: CAS:1008-95-3
Purity:98% HPLC Package:5G;10G;25G;50G;100G;250G;1KG
Company Name: Accela ChemBio Inc.
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Products Intro: Product Name:4-(5-Oxazolyl)aniline
CAS:1008-95-3
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Products Intro: Product Name:4-(1,3-Oxazol-5-yl)aniline
CAS:1008-95-3
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-09519
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4-(1,3-OXAZOL-5-YL)ANILINE manufacturers

4-(1,3-OXAZOL-5-YL)ANILINE Basic information
Product Name:4-(1,3-OXAZOL-5-YL)ANILINE
Synonyms:4-(5-Oxazolyl)aniline;4-(oxazol-5-yl)aniline;4-(1,3-OXAZOL-5-YL)ANILINE;5-(4-AMINOPHENYL)OXAZOLE;4-(1,3-Oxazol-5-yl)aniline, tech;4-(1,3-Oxazol-5-yl);4-Oxazol-5-yl-phenylamine;Benzenamine, 4-(5-oxazolyl)-
CAS:1008-95-3
MF:C9H8N2O
MW:160.17
EINECS:
Product Categories:Amines;Amines and Anilines;Heterocycles;Phenyls & Phenyl-Het;Phenyls & Phenyl-Het
Mol File:1008-95-3.mol
4-(1,3-OXAZOL-5-YL)ANILINE Structure
4-(1,3-OXAZOL-5-YL)ANILINE Chemical Properties
Melting point 150 °C
Boiling point 318.7±17.0 °C(Predicted)
density 1.204±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
pka3.46±0.10(Predicted)
form solid
color Pale yellow
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-36-22
Safety Statements 26-36/37/39
HazardClass IRRITANT
HS Code 2934999090
MSDS Information
4-(1,3-OXAZOL-5-YL)ANILINE Usage And Synthesis
Synthesis
5-(4-NITROPHENYL)-1,3-OXAZOLE

1014-23-9

4-(1,3-OXAZOL-5-YL)ANILINE

1008-95-3

General procedure for the synthesis of 4-(5-oxazolyl)aniline from 5-(4-nitrophenyl)oxazole: To a solution of ethanol (10 mL) containing 5-(4-nitrophenyl)oxazole (500 mg, 2.6 mmol) was added powdered tin (620 mg, 5.2 mmol), followed by the slow dropwise addition of concentrated hydrochloric acid (1 mL). The reaction mixture was stirred at room temperature for 2 hours. After completion of the reaction, the mixture was filtered and the filtrate was evaporated to dryness. The resulting residue was diluted with distilled water (10 mL) and alkalized to pH neutral with saturated sodium bicarbonate solution. Subsequently, the aqueous phase was extracted with ethyl acetate. The organic layer was separated, washed with distilled water, dried over anhydrous sodium sulfate and finally concentrated to dryness to give 4-(5-oxazolyl)aniline (380 mg, 90% yield) as a solid product.

References[1] Patent: WO2006/123145, 2006, A1. Location in patent: Page/Page column 66-67
[2] Patent: EP1612204, 2006, A1. Location in patent: Page/Page column 20
4-(1,3-OXAZOL-5-YL)ANILINE Preparation Products And Raw materials
Raw materials5-(4-NITROPHENYL)-1,3-OXAZOLE-->Hydrochloric acid-->Tin-->Water-->Ethanol
Tag:4-(1,3-OXAZOL-5-YL)ANILINE(1008-95-3) Related Product Information
5-(4-NITROPHENYL)-1,3-OXAZOLE 5-(4-NITRO-PHENYL)-OXAZOLE-4-CARBOXYLIC ACID ETHYL ESTER 5-(4-Nitrophenyl)oxazole-4-carboxylic acid 4-(1,3-OXAZOL-5-YL)ANILINE 4-[5-(4-DIMETHYLAMINOPHENYL)OXAZOL-2-YL]BENZENEBORONIC ACID 97 3-(1,3-OXAZOL-5-YL)ANILINE 2-(1,3-OXAZOL-5-YL)ANILINE 4-(2-METHYL-1,3-OXAZOL-5-YL)ANILINE 5-(2-METHOXY-4-NITROPHENYL)OXAZOLE 3-METHOXY-4-(1,3-OXAZOL-5-YL)ANILINE ETHYL 5-[(4N-BOC-AMINO)PHENYL]-1,3-OXAZOLE-4-CARBOXYLATE MERIMEPODIB 4-(2-CYCLOPROPYL-1,3-OXAZOL-5-YL)ANILINE 4-(BENZO[D]OXAZOL-2-YL)ANILINE 4-(4,5-DIHYDRO-1,3-OXAZOL-2-YL)ANILINE 4-(1,2-oxazol-5-yl)aniline 4-(1,3-OXAZOL-5-YL)PHENYL ISOTHIOCYANATE 5-(4-NITRO-PHENYL)-OXAZOL-2-YLAMINE

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