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Thermo Scientific Chemicals
3,5-Dichlorophenyl isocyanate, 97%
CAS: 34893-92-0 | C7H3Cl2NO | 188.007 g/mol
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Chemical Identifiers
CAS34893-92-0
IUPAC Name1,3-dichloro-5-isocyanatobenzene
Molecular FormulaC7H3Cl2NO
InChI KeyXEFUJGURFLOFAN-UHFFFAOYSA-N
SMILESClC1=CC(=CC(Cl)=C1)N=C=O
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Specifications
Specification Sheet
Specification SheetFormFused 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.
Applications
3,5-Dichlorophenyl isocyanate is used as an intermediate for medicine and in iprodione. It is also useful for proteomic research.
Solubility
Hydrolysis with water.
Notes
Light and moisture sensitive. Incompatible with water, alcohols, strong bases, amines, acids and strong oxidizing agents.
3,5-Dichlorophenyl isocyanate is used as an intermediate for medicine and in iprodione. It is also useful for proteomic research.
Solubility
Hydrolysis with water.
Notes
Light and moisture sensitive. Incompatible with water, alcohols, strong bases, amines, acids and strong oxidizing agents.
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.