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1-Cloro-4-nitrobenceno, +98 %, Thermo Scientific Chemicals

Thermo Scientific Chemicals

1-Cloro-4-nitrobenceno, +98 %, Thermo Scientific Chemicals

Name: 1-Cloro-4-nitrobenceno, +98 %, Thermo Scientific Chemicals
SKU: A15396.0I
Price: 237.00 EUR

CAS: 100-00-5 | C6H4ClNO2 | 157.553 g/mol

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Número de catálogo A15396.0I

también denominado A15396-0I

Precio (EUR)

237,00

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Cantidad:

5000 g

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Precio (EUR)

237,00

Each

Identificadores químicos

CAS100-00-5

IUPAC Name1-chloro-4-nitrobenzene

Molecular FormulaC6H4ClNO2

InChI KeyCZGCEKJOLUNIFY-UHFFFAOYSA-N

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

Especificaciones Specification Sheet

Hoja de especificaciones

FormCrystals or crystalline powder and/or coarse granular solid or flakes

Identification (FTIR)Conforms

Appearance (Color)White to yellow

Assay (GC)≥98.0%

Melting Point80.0-86.0?C

1-Chloro-4-nitrobenzene is an important intermediate used in the preparation of 2,4-dinitrochlorobenzene and 3,4-dichloronitrobenzene. It is used as a raw material in the preparation of 4-nitrodiphenylamine, 4-chloroaninline and (4-[(4-aminobenzene)sulfonyl]aniline). It serves as a common antioxidant, which is found in rubber.

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 1-cloro-4-nitrobenceno es un importante intermediario utilizado en la preparación de 2,4-dinitroclorobenceno y 3,4-dicloronitrobenceno. Se utiliza como materia prima en la preparación de 4-nitrodifenilamina, 4-cloroaninlina y (4-[(4-aminobenceno)sulfonil]anilina). Sirve como un antioxidante común, que se encuentra en el caucho.

Solubilidad
Soluble en etanol caliente hirviendo, éter, tolueno, acetona, disolventes orgánicos y disulfuro de carbono. Escasamente soluble en alcohol frío. Insoluble en agua.

Notas
Incompatible con agentes oxidantes fuertes y bases fuertes.

RUO – Research Use Only

General References:

The Cl substituent is activated to nucleophilic substitution by the p-nitro-group, and can be displaced under relatively mild conditions. For displacement by phenoxide, see: Org. Synth. Coll., 2, 445 (1943). For displacement by alkoxide in good yield, in the presence of TBAB or 18-crown-6, see: J. Org. Chem., 48, 3022 (1983).
Büldt, L. A.; Prescimone, A.; Neuburger, M.; Wenger, O. S. Photoredox Properties of Homoleptic d⁶ Metal Complexes with the Electron-Rich 4,4',5,5'-Tetramethoxy-2,2'-bipyridine Ligand. Eur. J. Inorg. Chem. 2015, 2015 (28), 4666-4677.
Zhuo, L.; Kou, K.; Yao, P.; Wu, G.; Wang, Y. Preparation and thermal decomposition kinetics research of pyridine-containing polyimide. J. Therm. Anal. Calorim. 2015, 119 (3), 2039-2051.