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Merck
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Key Documents

134198

Sigma-Aldrich

5-甲基-3-苯基异噁唑-4-羧酸

99%

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About This Item

經驗公式(希爾表示法):
C11H9NO3
CAS號碼:
分子量::
203.19
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:

品質等級

化驗

99%

mp

192-194 °C (lit.)

SMILES 字串

Cc1onc(-c2ccccc2)c1C(O)=O

InChI

1S/C11H9NO3/c1-7-9(11(13)14)10(12-15-7)8-5-3-2-4-6-8/h2-6H,1H3,(H,13,14)

InChI 密鑰

PENHKTNQUJMHIR-UHFFFAOYSA-N

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應用

5-Methyl-3-phenylisoxazole-4-carboxylic acid was used in preparation of intermediates for the synthesis of penicillin. It was used for acylation during solid support synthesis of the isoxazolopyridone derivatives.

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


分析證明 (COA)

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1112. Derivatives of 6-aminopenicillanic acid. Part VI. Penicillins from 3-and 5-phenylisoxazole-4-carboxylic acids and their alkyl and halogen derivatives.
Doyle FP, et al.
Journal of the Chemical Society, 5838-5845 (1963)
Masayuki Nakamura et al.
Bioorganic & medicinal chemistry letters, 20(2), 726-729 (2009-12-17)
This Letter describes the synthesis and evaluation of mGluR7 antagonists in the isoxazolopyridone series. In the course of modification in this class, novel solid support synthesis of the isoxazolopyridone scaffold was developed. Subsequent chemical modification led to the identification of

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