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Ethyl 5-amino-4-phenylisoxazole-3-carboxylate

CAS No.
53983-15-6
Chemical Name:
Ethyl 5-amino-4-phenylisoxazole-3-carboxylate
Synonyms
Ethyl 5-amino-4-phenyl-3-isoxazolecarboxylate;ethyl 5-amino-4-phenyl-1,2-oxazole-3-carboxylate;5-amino-4-phenyl-3-Isoxazolecarboxylic acid ethyl ester;3-Isoxazolecarboxylic acid, 5-amino-4-phenyl-, ethyl ester
CBNumber:
CB51116574
Molecular Formula:
C12H12N2O3
Molecular Weight:
232.24
MDL Number:
MFCD06199347
MOL File:
53983-15-6.mol
Last updated:2026-05-28 02:10:59

Ethyl 5-amino-4-phenylisoxazole-3-carboxylate Properties

storage temp. 2-8°C(protect from light)

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338

Ethyl 5-amino-4-phenylisoxazole-3-carboxylate price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Biosynth DCA98315 ethyl 5-amino-4-phenyl-1,2-oxazole-3-carboxylate 53983-15-6 2.5g $413 2026-06-04 Buy
Matrix Scientific 301076 Ethyl 5-amino-4-phenylisoxazole-3-carboxylate 53983-15-6 250.00mg $49 2026-05-19 Buy
Matrix Scientific 301076 Ethyl 5-amino-4-phenylisoxazole-3-carboxylate 53983-15-6 1.00g $99 2026-05-19 Buy
Matrix Scientific 301076 Ethyl 5-amino-4-phenylisoxazole-3-carboxylate 53983-15-6 5.00g $343 2026-05-19 Buy
Synthonix E55720 Ethyl 5-amino-4-phenylisoxazole-3-carboxylate 97% 53983-15-6 250mg $120 2026-05-06 Buy
Product number Packaging Price Buy
DCA98315 2.5g $413 Buy
301076 250.00mg $49 Buy
301076 1.00g $99 Buy
301076 5.00g $343 Buy
E55720 250mg $120 Buy

Ethyl 5-amino-4-phenylisoxazole-3-carboxylate Chemical Properties,Uses,Production

Synthesis

Benzenepropanoic acid, β-methyl-, ethyl ester, (βS)-

1134-71-0

Ethyl 5-amino-4-phenylisoxazole-3-carboxylate

53983-15-6

General procedure for the synthesis of ethyl 5-amino-4-phenylisoxazole-3-carboxylate from the compound (CAS: 1134-71-0): phenylpropyl derivative 1 (12 mmol), hydroxylamine hydrochloride (1.66 g, 24 mmol) and 70 mL of ethanol were mixed and heated and refluxed for 12 hours. Upon completion of the reaction, the ethanol was removed by distillation under reduced pressure. Subsequently, 50 mL of ethyl acetate and 10 mL of 10% sodium carbonate solution were added to the residue and mixed thoroughly to separate the organic phase. The organic phase was washed with saturated sodium chloride solution and dried with anhydrous sodium sulfate. Finally, the ethyl acetate was removed by evaporation under reduced pressure to give 2.48 g of white powdery solid product in 89.11% yield.

References

[1] Patent: CN105777661, 2016, A. Location in patent: Paragraph 0041; 0042; 0043

Ethyl 5-amino-4-phenylisoxazole-3-carboxylate Preparation Products And Raw materials

Ethyl 5-amino-4-phenylisoxazole-3-carboxylate Suppliers

Global( 21)Suppliers
Supplier Tel Email Country ProdList Advantage
HBCChem, Inc. +1-510-219-6317 sales@hbcchem.com United States 10628 60
Cool Pharm, Ltd 021-60455363 18019463053 sales@coolpharm.com China 8455 58
Zhengzhou Guancheng Laboratory equipment Sales 0371-88888888 qq272369594;2159423853qq 2723695949@qq.com China 4991 50
Amadis Chemical Company Limited 571-89925085 sales@amadischem.com China 131885 58
Energy Chemical 021-58432009 400-005-6266 marketing@energy-chemical.com China 44871 58
Jiangsu Nanchuang Chemical and Life Health Research Institute Co., Ltd. 15720605021 zhang_lei@jsnchem.com China 1881 58
Beijing Stronger Science Co., Ltd. 0531-88924771 15614660963 elsa.hang@strongerscience.com China 10622 58
Bide Pharmatech Ltd. 400-1647117 13681763483 product02@bidepharm.com China 59929 58
Bide Pharmatech Ltd. 400-6005915 sales@picasso-e.com China 39645 58
Zhengzhou Converging Chemical Co. LTD 0371-53399770 18037166334 3857571523@qq.com China 7099 58
5-amino-4-phenyl-3-Isoxazolecarboxylic acid ethyl ester 3-Isoxazolecarboxylic acid, 5-amino-4-phenyl-, ethyl ester Ethyl 5-amino-4-phenyl-3-isoxazolecarboxylate ethyl 5-amino-4-phenyl-1,2-oxazole-3-carboxylate 53983-15-6