BENZOOXAZOLE-2-CARBOXYLIC ACID METHYL ESTER

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Products Intro: Product Name:METHYL BENZO[D]OXAZOLE-2-CARBOXYLATE
CAS:27383-86-4
Purity:99% Package:100kg;2USD|10kg;4USD|1kg;6USD
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Products Intro: Product Name:Methyl benzooxazole-2-carboxylate
CAS:27383-86-4
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CAS:27383-86-4
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Products Intro: Product Name:methyl 1,3-benzoxazole-2-carboxylate
CAS:27383-86-4
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Products Intro: Product Name:METHYL BENZOOXAZOLE-2-CARBOXYLATE
CAS:27383-86-4
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BENZOOXAZOLE-2-CARBOXYLIC ACID METHYL ESTER manufacturers

BENZOOXAZOLE-2-CARBOXYLIC ACID METHYL ESTER Basic information
Product Name:BENZOOXAZOLE-2-CARBOXYLIC ACID METHYL ESTER
Synonyms:BENZOOXAZOLE-2-CARBOXYLIC ACID METHYL ESTER;Methyl 1,3-benzoxazole-2-carboxylate;Methyl benzo[d]oxazole-2-carboxylate;2-Benzoxazolecarboxylic acid, Methyl ester;Methyl 2-benzoxazolecarboxylate
CAS:27383-86-4
MF:C9H7NO3
MW:177.16
EINECS:
Product Categories:
Mol File:27383-86-4.mol
BENZOOXAZOLE-2-CARBOXYLIC ACID METHYL ESTER Structure
BENZOOXAZOLE-2-CARBOXYLIC ACID METHYL ESTER Chemical Properties
Melting point 99 °C
Boiling point 272.3±23.0 °C(Predicted)
density 1.288±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka0.14±0.10(Predicted)
AppearanceWhite to light brown Solid
InChIInChI=1S/C9H7NO3/c1-12-9(11)8-10-6-4-2-3-5-7(6)13-8/h2-5H,1H3
InChIKeyYDKNBNOOCSNPNS-UHFFFAOYSA-N
SMILESO1C2=CC=CC=C2N=C1C(OC)=O
Safety Information
HS Code 2934999090
MSDS Information
BENZOOXAZOLE-2-CARBOXYLIC ACID METHYL ESTER Usage And Synthesis
UsesMethyl Benzo[D]oxazole-2-carboxylate is used as a reactant in the preparation of benzoxazole-based oxadiazoles as antimicrobial agents.
Synthesis
Benzoxazole

273-53-0

Carbon dioxide

124-38-9

Iodomethane

74-88-4

BENZOOXAZOLE-2-CARBOXYLIC ACID METHYL ESTER

27383-86-4

Catalyst (9.9 mg, 0.025 mmol, 5 mol%), potassium tert-butoxide (0.0672 g, 0.6 mmol) and DMF (3.0 mL) were added to the reaction flask under argon protection. Benzoxazole (50.7 μL, 0.5 mmol) was then added and carbon dioxide gas was passed under atmospheric pressure. The reaction mixture was stirred at 80 °C for 18 hours. After completion of the reaction, the temperature was lowered to 65 °C, iodomethane (93 μL, 1.5 mmol) was added, and stirring was continued at 65 °C for 1 h. The reaction was carried out with the aid of deionized water. At the end of the reaction, the reaction was quenched with deionized water and the reaction product was extracted with ethyl acetate. The yield of the product, methyl benzo[d]oxazole-2-carboxylate, was measured to be 95% by gas chromatography analysis. Further purification by column chromatography using ethyl acetate/petroleum ether (1:10, v/v) as the unfolding solvent gave 90% yield of the purified product.

References[1] Green Chemistry, 2018, vol. 20, # 5, p. 989 - 996
[2] Organic Letters, 2010, vol. 12, # 15, p. 3567 - 3569
[3] Journal of the American Chemical Society, 2010, vol. 132, # 26, p. 8858 - 8859
[4] Patent: CN106565623, 2017, A. Location in patent: Paragraph 0021
[5] Angewandte Chemie - International Edition, 2010, vol. 49, # 46, p. 8670 - 8673
BENZOOXAZOLE-2-CARBOXYLIC ACID METHYL ESTER Preparation Products And Raw materials
Raw materialsMethanol-->Benzoxazole-->Methyl [(2-hydroxyphenyl)carbamoyl]formate-->Carbon dioxide-->2-Benzoxazolecarbonyl chloride (9CI)-->Iodomethane-->Potassium tert-butoxide-->N,N-Dimethylformamide
Tag:BENZOOXAZOLE-2-CARBOXYLIC ACID METHYL ESTER(27383-86-4) Related Product Information
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