Nombre del producto:3-(1H-Indol-3-yl)-2-(5-methylfuran-2-carboxamido)propanoic acid

IUPAC Name:3-(1H-indol-3-yl)-2-[(5-methylfuran-2-yl)formamido]propanoic acid

CAS:360573-13-3
Fórmula molecular:C17H16N2O4
Pureza:97%
Número de catálogo:CM263803
Peso molecular:312.33

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Detalles del producto

Núm. De CAS :360573-13-3
Fórmula molecular:C17H16N2O4
Punto de fusión:-
Código de sonrisas:O=C(O)C(NC(C1=CC=C(C)O1)=O)CC2=CNC3=C2C=CC=C3
Densidad:
Número de catálogo:CM263803
Peso molecular:312.33
Punto de ebullición:
Nº Mdl:MFCD01141154
Almacenamiento:

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Amino Acids and Peptides
Amino acids are organic compounds containing a basic amino group and an acidic carboxyl group. Because amino acids contain both amino and carboxyl groups, they can be polymerized in an end-to-end manner, removing a molecule of water to form a covalent amide bond or peptide bond. Many amino acids are linked together end to end to form a polypeptide. Amino acids and peptides are important components in the fields of medicine and life sciences.
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Indoles
Indole is a compound of pyrrole and benzene in parallel, also known as benzopyrrole. There are two combinations of pyrrole and benzene, called indole and isoindole, respectively. Many derivatives of indole have physiological and pharmacological activities, and can synthesize vasodilators, antihistamines, antipyretic analgesics, etc. in medicine, so indole is also a very important heterocyclic compound.
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Furans
Furan is a cyclic flammable liquid compound C4H4O that is obtained from wood oils of pines or made synthetically and is used especially in organic synthesis. Furan is aromatic because a pair of lone pair electrons of the oxygen atom in its molecule forms a large π bond in the plane of the conjugated orbital, making a total of 6 electrons in the plane of the conjugated plane, conforming to the 4n+2 structure. Aromaticity makes furan have the property of easy substitution and difficult addition. The other lone pair of electrons in oxygen stretches out. The oxygen atom itself conforms to sp2 hybridization. Due to the presence of the aromatic ring, the chemical behavior of furan is not very similar to that of other unsaturated heterocycles. The oxygen in the aromatic ring has an electron-donating effect, so the electrophilic substitution reactivity of furan is stronger than that of benzene.
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