Ácido 4-isopropoxibenzoico, 99 %, Thermo Scientific Chemicals
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Ácido 4-isopropoxibenzoico, 99 %, Thermo Scientific Chemicals
Ácido 4-isopropoxibenzoico, 99 %, Thermo Scientific Chemicals
Ácido 4-isopropoxibenzoico, 99 %, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Ácido 4-isopropoxibenzoico, 99 %, Thermo Scientific Chemicals

CAS: 13205-46-4 | C10H12O3 | 180.203 g/mol
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Cantidad:
10 g
50 g
250 g
Número de catálogo A14351.18
también denominado A14351-18
Precio (USD)
-
Cantidad:
50 g
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Identificadores químicos
CAS13205-46-4
IUPAC Name4-(propan-2-yloxy)benzoic acid
Molecular FormulaC10H12O3
InChI KeyZVERWTXKKWSSHH-UHFFFAOYSA-N
SMILESCC(C)OC1=CC=C(C=C1)C(O)=O
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EspecificacionesSpecification SheetHoja de especificaciones
Appearance (Color)White
FormCrystals or powder or crystalline powder
Assay (Aqueous acid-base Titration)≥98.5 to ≤101.5%
Assay (HPLC)≥98.5%
Melting Point (clear melt)161.0-167.0?C
4-Isopropoxybenzoic acid is used to prepare 5-(4-isopropoxyphenyl)-N-phenyl-1,3,4-thiadiazol-2-amine by reacting with N-phenylhydrazinecarbothioamide in the presence of phosphorusoxychloride.

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.

Aplicaciones
El ácido 4-isopropoxibenzoico se utiliza para preparar 5-(4-isopropoxifenil)-N-fenil-1,3,4-tiadiazol-2-amina mediante la reacción con N-fenilhidracinacarbotioamida en presencia de oxicloruro de fósforo.

Solubilidad
Insoluble en agua.

Notas
Incompatible con agentes oxidantes fuertes.
RUO – Research Use Only

General References:

  1. Neubauer, S.; Rechenmacher, F.; Brimioulle, R.; Di Leva, F. S.; Bochen, A.; Sobahi, T. R.; Schottelius, M.; Novellino, E.; Mas-Moruno, C.; Marinelli, L.; Kessler, H. Pharmacophoric Modifications Lead to Superpotent alphavbeta3 Integrin Ligands with Suppressed alpha5beta1 Activity. J. Med. Chem. 2014, 57 (8), 3410-3417.
  2. Croxall, W. J.; Sowa, F. J.; Nieuwland, J. A. Organic Reactions with Boron Fluoride. XI. The Condensation of Propylene with m-and p-Hydroxybenzoic Acids. J. Am. Chem. Soc. 1935, 57 (9), 1549-1551.