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TCI

CAS 75-29-6

2-Chloropropane TCI C0267

2-Chloropropane TCI C0267

Chemical Identity

Other names
Isopropyl Chloride
CAS No.
75-29-6
PubChem
CID 6361·SID 87565423
Formula
C3H7Cl
Molecular weight
78.54 g/mol
Purity
>99.0%(GC)
Reference databases
ChemSpider·ECHA·Wikipedia
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
2-chloropropane
SMILES
CC(C)Cl
InChIKey
ULYZAYCEDJDHCC-UHFFFAOYSA-N
MDL
MDL00000867
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TCI C0267 2-Chloropropane (CAS 75-29-6) is the secondary isomer of chloropropane and a convenient source of the isopropyl group in synthesis. It is used in isopropylation reactions, Friedel–Crafts alkylation, and the preparation of isopropyl organometallic reagents. Its secondary structure also makes it a valuable teaching example when comparing substitution and elimination pathways. Supplied in 25 mL and 500 mL packs, this highly flammable liquid must be handled in a fume hood away from all ignition sources.

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  • Saheb (2013). Theoretic studies on the kinetics and mechanism of multi-channel gas-phase unimolecular reactions of 1-chloropropane and 2-chloropropane. Structural Chemistry doi:10.1007/s11224-013-0240-2
  • Ermacora et al. (2014). Influence of oil composition on the formation of fatty acid esters of 2-chloropropane-1,3-diol (2-MCPD) and 3-chloropropane-1,2-diol (3-MCPD) under conditions simulating oil refining. Food Chemistry doi:10.1016/j.foodchem.2014.03.130
  • Gronert (1993). Theoretical studies of elimination reactions. 3. Gas-phase reactions of fluoride ion with 2-chloropropane and 1-chloropropane. The effect of methyl substituents. Journal of the American Chemical Society doi:10.1021/ja00055a039

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