CAS 2124-55-2
:ácido indol-4-carboxílico
Descripción:
ácido indol-4-carboxílico es un compuesto orgánico caracterizado por su estructura de indol, que consiste en un anillo de benceno y un anillo de pirrol fusionados, con un grupo funcional de ácido carboxílico unido en la cuarta posición del anillo de indol. Este compuesto es típicamente un sólido blanco a blanco sucio y es soluble en disolventes polares como agua y alcoholes, debido a la presencia del grupo ácido carboxílico. ácido indol-4-carboxílico es conocido por su papel en varios procesos bioquímicos y puede servir como precursor en la síntesis de productos farmacéuticos y agroquímicos. Exhibe potenciales actividades biológicas, incluyendo propiedades antimicrobianas y antiinflamatorias, lo que lo hace de interés en la química medicinal. Además, sus derivados pueden ser explorados por sus aplicaciones en síntesis orgánica y ciencia de materiales. Al igual que muchos derivados de indol, la reactividad del compuesto puede verse influenciada por la presencia de sustituyentes en el anillo de indol, lo que permite diversas transformaciones químicas.
Fórmula:C9H6NO2
InChI:InChI=1/C9H7NO2/c11-9(12)7-2-1-3-8-6(7)4-5-10-8/h1-5,10H,(H,11,12)/p-1
SMILES:c1cc(c2cc[nH]c2c1)C(=O)[O-]
Sinónimos:- 1H-Indole-4-Carboxylic Acid
- 1H-4-Indolecarboxylic Acid
- 4-Indolecarboxylic Acid
- 4-Carboxyindole
- Rarechem Al Be 1201
- Indole-4-Carbocylic Acid
- 4-Indole Carboxylic Acid
- Indole-4-Carboxylicacid
- 1H-Indole-4-Carboxylate
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Encontrado 7 productos.
Indole-4-carboxylic Acid
CAS:Fórmula:C9H7NO2Pureza:>98.0%(GC)(T)Forma y color:White to Gray to Brown powder to crystalPeso molecular:161.161H-Indole-4-carboxylic acid
CAS:1H-Indole-4-carboxylic acidFórmula:C9H7NO2Pureza:98%Forma y color: lumpy. salmon/light tan powderPeso molecular:161.16g/molIndole-4-carboxylic acid
CAS:Indole-4-Carboxylic acid is a molecule that belongs to the group of indole carboxylic acids. It is an organic compound that has a dipole moment and isomers. Indole-4-carboxylic acid can be synthesized by the saponification of indole-7-carboxylic acid, which has two functional groups: a hydroxy group and an amide group. The molecule has a chemical structure with an amide bond between the carboxyl and amino groups at one end, which forms a protonated amide. This protonated amide also has two orientations: trans and cis. The trans orientation is found in human cytochrome P450 and other proteins, while the cis orientation is found in enzymes such as tryptophan synthase, indoleamine 2,3 dioxygenase, or tyrosine hydroxylase.
Fórmula:C9H7NO2Pureza:Min. 98 Area-%Forma y color:PowderPeso molecular:161.16 g/molIndole-4-carboxylic acid
CAS:Indole-4-carboxylic acid is a fine chemical that is used as a versatile building block for organic synthesis. It is an important intermediate for the synthesis of other compounds and has been used in the preparation of research chemicals, such as indoles, benzimidazoles, and benzoxazoles. As a speciality chemical, it can be used as a reagent in several chemical reactions. Indole-4-carboxylic acid is also useful as a reaction component in the manufacture of pharmaceuticals, agrochemicals, dyestuffs, and pigments. In addition to being an intermediate for many other compounds, it can be used to make new drugs with potential use in cancer therapy.Fórmula:C9H7NO2Peso molecular:161.16 g/molRef: 3D-I-2330
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