4-bromo-3-fluoro-2-methylbenzonitrile

4-bromo-3-fluoro-2-methylbenzonitrile

(4-butoxyphenyl)methanol

(4-butoxyphenyl)methanol

4-bromophenyl isothiocyanate

$300.00
CAS No.: 1985-12-2
Catalog No.: WLZ1749
Purity: 95%
MF: C7H4BrNS
MW: 214.087
Storage: 2-8 degree Celsius
SMILES: BrC1=CC=C(C=C1)N=C=S
For R&D use only. Not for human or animal use.
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CAS NO.: 1985-12-2; 4-bromophenyl isothiocyanate. PROPERTIES: This brominated aromatic isothiocyanate features a bromine atom on a phenyl ring connected to an isothiocyanate group, creating a molecule with potential applications in organic synthesis and agrochemical research. The 4-bromophenyl isothiocyanate typically appears as a colorless to pale yellow liquid with moderate solubility in common organic solvents. Its molecular structure includes a reactive isothiocyanate group that can participate in various chemical reactions. For optimal stability and to prevent premature reactions, this compound should be stored at 2-8 degree Celsius in an amber glass bottle under an inert atmosphere. When handling, appropriate safety measures including nitrile gloves and safety goggles are recommended. This compound is sensitive to light and moisture, requiring careful environmental control during storage and use. In case of skin contact, wash thoroughly with soap and water; if eye contact occurs, rinse immediately and seek medical evaluation. APPLICATIONS: The 4-bromophenyl isothiocyanate serves as a versatile building block in organic synthesis, particularly for creating thiourea and rhodanine derivatives. The isothiocyanate group provides a handle for nucleophilic addition reactions. In agrochemical research, this compound functions as an intermediate for developing herbicides and fungicides where the thiocarbonyl functionality contributes to target binding and efficacy. Additionally, the molecule finds utility in medicinal chemistry as a precursor for creating enzyme inhibitors and receptor modulators. Researchers utilizing this compound can benefit from its functional group versatility, enabling the development of diverse molecular architectures for applications ranging from agrochemicals to pharmaceuticals.

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