3,5-Diclorofenilo isocianato, 97 %, Thermo Scientific Chemicals

Name: 3,5-Diclorofenilo isocianato, 97 %, Thermo Scientific Chemicals
SKU: A19991.06
Price: 89.70 EUR

CAS: 34893-92-0 | C7H3Cl2NO | 188.007 g/mol

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Cantidad:

5 g

25 g

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Número de catálogo A19991.06

también denominado A19991-06

Precio (EUR)

89,70

Each

Cantidad:

5 g

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Precio (EUR)

89,70

Each

Identificadores químicos

CAS34893-92-0

IUPAC Name1,3-dichloro-5-isocyanatobenzene

Molecular FormulaC7H3Cl2NO

InChI KeyXEFUJGURFLOFAN-UHFFFAOYSA-N

SMILESClC1=CC(=CC(Cl)=C1)N=C=O

Especificaciones Specification Sheet

Hoja de especificaciones

FormFused solid or clear liquid as melt

Identification (FTIR)Conforms

Appearance (Color)White to pale yellow

Assay (GC)≥96.0%

Melting Point (clear melt)26.0-35.0?C

3,5-Dichlorophenyl isocyanate is used as an intermediate for medicine and in iprodione. It is also useful for proteomic research.

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 isocianato de 3,5-diclorofenilo se utiliza como intermediario para la medicina y en la iprodiona. También es útil para la investigación proteómica.

Solubilidad
Hidrólisis con agua.

Notas
Sensible a la luz y la humedad. Incompatible con agua, alcoholes, bases fuertes, aminas, ácidos y agentes oxidantes fuertes.

RUO – Research Use Only

General References:

Singhal, S. S.; Figarol, J.; Singhal, J.; Nagaprashanth, L. N.; Berz, D.; Rahbar, S.; Awasthi, S. Novel compound 1,3-bis (3,5-dichlorophenyl) urea inhibits lung cancer progression. Biochem. Pharmacol. 2013, 86 (12), 1664-1672.
Uraguchi, D.; Tsutsumi, R.; Ooi, T. Catalytic Asymmetric Oxidation of N-Sulfonyl Imines with Hydrogen Peroxide-Trichloroacetonitrile System. J. Am. Chem. Soc. 2013, 135 (22), 8161-8164.
Johnson, A.; Saundersa, M. J.; Back, T. G. Stereodivergent synthesis of the LFA-1 antagonist BIRT-377 by porcine liver esterase desymmetrization and Curtius rearrangement. Org. Biomol. Chem. 2015, 13 (5), 1463-1469.