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Isoxazole-5-carboxylic acid, 98%, Thermo Scientific Chemicals

Catalog Number 11474764
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Quantity:
1 g
5 g
25 g
This item is not returnable. View return policy
21169-71-1
C4H3NO3
113.072
MFCD00156151
MIIQJAUWHSUTIT-UHFFFAOYSA-N
isoxazole-5-carboxylic acid, 5-isoxazolecarboxylic acid, isoxazole-5-carboxylicacid, 5-carboxyisoxazole, pubchem8643, isoxazole-5-carboxylic, 5-carboxy-1,2-oxazole, isoxazole 5-carboxylic acid, ksc207s2h
2060599
1,2-oxazole-5-carboxylic acid
C1=C(ON=C1)C(=O)O
This item is not returnable. View return policy
21169-71-1
C4H3NO3
113.072
MFCD00156151
MIIQJAUWHSUTIT-UHFFFAOYSA-N
isoxazole-5-carboxylic acid, 5-isoxazolecarboxylic acid, isoxazole-5-carboxylicacid, 5-carboxyisoxazole, pubchem8643, isoxazole-5-carboxylic, 5-carboxy-1,2-oxazole, isoxazole 5-carboxylic acid, ksc207s2h
2060599
1,2-oxazole-5-carboxylic acid
C1=C(ON=C1)C(=O)O

Reaction conditions were found to allow the exclusive formation of isoxazole-5-carboxylic acid derivatives by conjugate addition, in acidic medium, of hydroxylamine to β-alkoxyvinyl trichloromethyl ketone in synthesis and reactivity of isoxazoles. Isoxazole-5-carboxylic acid participates in the Synthesis and evaluation of acylguanidine FXa inhibitors. 1, 1, 1-trichloro-4-methoxy-3-penten-2-one postulated in the preparation of isoxazole-5-carboxylic acid from trichloroacetyl chloride, ethyl vinyl ether and hydroxylamine is developed in a fully saturated nitrogen atom theerefore there is no possibility of conjugation with 4- substituents.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Reaction conditions were found to allow the exclusive formation of isoxazole-5-carboxylic acid derivatives by conjugate addition, in acidic medium, of hydroxylamine to β-alkoxyvinyl trichloromethyl ketone in synthesis and reactivity of isoxazoles. Isoxazole-5-carboxylic acid participates in the Synthesis and evaluation of acylguanidine FXa inhibitors. 1, 1, 1-trichloro-4-methoxy-3-penten-2-one postulated in the preparation of isoxazole-5-carboxylic acid from trichloroacetyl chloride, ethyl vinyl ether and hydroxylamine is developed in a fully saturated nitrogen atom theerefore there is no possibility of conjugation with 4- substituents.

Solubility
Slightly soluble in water.

Notes
Moisture Sensitive. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents, reducing agents, bases.
TRUSTED_SUSTAINABILITY
Melting Point 141°C to 144°C
Quantity 5 g
Solubility Information Slightly soluble in water.
Formula Weight 113.07
Percent Purity 98%
Chemical Name or Material Isoxazole-5-carboxylic acid

RUO – Research Use Only

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