4-Nitrobenzyl Chloride TCI C0229

Chemical Identity

Other names: alpha-Chloro-4-nitrotoluene
CAS No.: 100-14-1
Formula: C7H6ClNO2
Molecular weight: 171.58 g/mol
Purity: >98.0%(GC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 1-(chloromethyl)-4-nitrobenzene
SMILES: C1=CC(=CC=C1CCl)[N+](=O)[O-]
InChIKey: KGCNHWXDPDPSBV-UHFFFAOYSA-N
MDL: MDL00007374
PubChem: CID 7482

Rp 1.060.500,00

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Berat 25g 250g

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TCI C0229 4-Nitrobenzyl Chloride (CAS 100-14-1) is a non-heterocyclic building block widely used in organic synthesis laboratories. Its activated benzylic chloride readily alkylates oxygen, nitrogen, and sulfur nucleophiles, while the para-nitro group provides a strong ultraviolet chromophore. Researchers commonly apply it to derivatize carboxylic acids for HPLC detection and to install a removable protecting group during multistep synthesis. AMI Scientific supplies this TCI reagent in 25 g and 250 g packs for academic, pharmaceutical, and industrial research use.

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JENSEN et al. (1998). ChemInform Abstract: Solvent Effects on the Reduction Mechanism of 9‐Chloroanthracene, 3‐Nitrobenzyl Chloride, and 3‐Chloroacetophenone.. ChemInform doi:10.1002/chin.199851067
Giuglio‐Tonolo et al. (2003). Original Reaction of p‐Nitrobenzyl Chloride with Aldehydes Using Tetrakis(dimethylamino)ethylene (TDAE).. ChemInform doi:10.1002/chin.200347095
BARELMANN et al. (1991). ChemInform Abstract: Simultaneous Electrochemical Electron Paramagnetic Resonance Investigation of the Reduction of p‐Nitrobenzyl Chloride.. ChemInform doi:10.1002/chin.199103049

References were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.