Cyclopropylamine TCI C0981

Chemical Identity

Other names: Aminocyclopropane
CAS No.: 765-30-0
PubChem: CID 69828·SID 87566026
Formula: C3H7N
Molecular weight: 57.10 g/mol
Purity: >95.0%(GC)(T)
Reference databases: ChEBI·ChemSpider·ECHA·Wikipedia

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: cyclopropanamine
SMILES: C1CC1N
InChIKey: HTJDQJBWANPRPF-UHFFFAOYSA-N
MDL: MDL00001301

Rp 822.150,00

~~Rp 590.100,00~~ Rp 822.150,00

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Volume 5mL 25mL

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TCI C0981 Cyclopropylamine (CAS 765-30-0) is a volatile primary amine bearing a strained three-membered ring, supplied in 5 mL and 25 mL bottles. Its nucleophilic amine reacts readily to form amides, sulfonamides, ureas, carbamates, and aromatic substitution products. The N-cyclopropyl motif is a well-known feature in medicinal chemistry, notably within quinolone antibacterial scaffolds. The material is highly flammable and corrosive, so handle it in a fume hood away from ignition sources and keep it tightly closed under cool storage.

TCI brochures (PDF)

Plant-Based Environmental-Friendly Organocatalyst for Asymmetric Ring-Opening Reaction of Epoxides 2024-09-30 · p. 1

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Davidson et al. (1991). Inhibition by cyclopropylamine of the quinoprotein methylamine dehydrogenase is mechanism-based and causes covalent crosslinking of .alpha. and .beta. subunits. Biochemistry doi:10.1021/bi00221a027
Manakhov et al. (2014). Cyclopropylamine plasma polymers deposited onto quartz crystal microbalance for biosensing application. physica status solidi (a) doi:10.1002/pssa.201431399
Mao et al. (2014). ChemInform Abstract: Asymmetric Synthesis of Cyclopropylamine Derivatives. ChemInform doi:10.1002/chin.201439269

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