CAS 97271-97-1

Fórmula: C7H6N2O3

InChI: InChI=1S/C7H6N2O3/c8-7-5(4-10)2-1-3-6(7)9(11)12/h1-4H,8H2

Clave InChI: LDKGAMZVANIDGZ-UHFFFAOYSA-N

SMILES: C1=CC(=C(C(=C1)[N+](=O)[O-])N)C=O

2-Amino-3-nitrobenzaldehyde

CAS: 97271-97-1

2-Amino-3-nitrobenzaldehyde

Fórmula: C₇H₆N₂O₃

Pureza: 98%

Peso molecular: 166.13

Ref: 54-OR80021

2-Amino-3-nitrobenzaldehyde

CAS: 97271-97-1

Fórmula: C₇H₆N₂O₃

Pureza: 98%

Forma y color: Solid

Peso molecular: 166.1341

Ref: IN-DA00IJXA

2-Amino-3-nitrobenzaldehyde

CAS: 97271-97-1

2-Amino-3-nitrobenzaldehyde

Fórmula: C₇H₆N₂O₃

Pureza: 98%

Peso molecular: 166.13

Ref: IN-DG234192

2-Amino-3-nitrobenzaldehyde

CAS: 97271-97-1

Fórmula: C₇H₆N₂O₃

Pureza: 98%

Peso molecular: 166.136

Ref: 10-F229178

2-Amino-3-nitrobenzaldehyde

CAS: 97271-97-1

2-Amino-3-nitrobenzaldehyde is an organic compound that contains a quinoline ring. It is the product of the oxidative coupling of 2-amino-3-nitrobenzoic acid and hydrogen peroxide. The reaction mechanism begins with epoxidation of the quinoline ring, followed by a nitration to form 7-nitroindole. The 8-nitroquinoline is formed from an oxidation of the 7-nitroindole, which then undergoes hydrogenation to form 2-amino-3-nitrobenzaldehyde. This reaction can be used in elucidating the molecular structure of 8-nitroquinoline.

Fórmula: C₇H₆N₂O₃

Pureza: Min. 95%

Peso molecular: 166.14 g/mol

Ref: 3D-XDA27197