missing translation for 'onlineSavingsMsg'
Learn More

Isoxazole-5-carboxylic acid, 98%

Codice prodotto. 11474764
Cambia vista
Click to view available options
Quantità:
1 g
5 g
25 g
Dimensione della confezione:
1g
25g
5g
3 product options available for selection
Product selection table with 3 available options. Use arrow keys to navigate and Enter or Space to select.
Codice prodotto. Quantità unitSize
11474764 5 g 5g
11464764 1 g 1g
11484764 25 g 25g
Use arrow keys to navigate between rows. Press Enter or Space to select a product option. 3 options available.
3 options
Les retours ne sont pas autorisés pour ce produit. Consulta la politica di reso
Codice prodotto. 11474764 Fornitore Thermo Scientific Alfa Aesar N. del fornitore A13739.06
Richiesta di formato massivo o personalizzato

Please to purchase this item. Need a web account? Register with us today!

Les retours ne sont pas autorisés pour ce produit. Consulta la politica di reso

CAS: 21169-71-1 | C4H3NO3 | 113.072 g/mol

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

Identificatori chimici

CAS 21169-71-1
Formula molecolare C4H3NO3
Molecular Weight (g/mol) 113.072
Numero MDL MFCD00156151
InChI Key MIIQJAUWHSUTIT-UHFFFAOYSA-N
Sinonimo 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
PubChem CID 2060599
IUPAC Name 1,2-oxazole-5-carboxylic acid
SMILES C1=C(ON=C1)C(=O)O

Specifica

Materiale o nome chimico Isoxazole-5-carboxylic acid
Punto di fusione 141°C to 144°C
Quantità 5 g
Informazioni di solubilità Slightly soluble in water.
Peso formulazione 113.07
Percent Purity 98%

RUO – Research Use Only

Titolo del prodotto
Selezionare un problema

Facendo clic su Invia, l'utente riconosce che potrebbe essere contattato da Fisher Scientific in merito al feedback fornito in questo modulo. Non condivideremo le vostre informazioni per altri scopi. Tutte le informazioni di contatto fornite saranno conservate in conformità con la nostra Politica sulla privacy. Informativa sulla privacy.