TCI C0982 Cyclopropanemethanol (CAS 2516-33-8) is a primary alcohol attached to a strained cyclopropane ring, supplied in 5 mL and 25 mL bottles. The hydroxyl group is readily oxidized, esterified, etherified, or converted into a leaving group for alkylation chemistry. This makes it a convenient way to install a rigid, compact cyclopropylmethyl fragment in pharmaceutical and agrochemical research. Handle it in a fume hood with gloves and eye protection, and store it tightly closed in a cool, dry, well-ventilated area away from ignition sources.
Related TCI products
- TCI M1412 34885-03-5 4-Methyl-1-cyclohexanemethanol (cis- and trans- mixture)
- TCI M1136 3143-02-0 3-Methyl-3-oxetanemethanol
- TCI E0546 3047-32-3 3-Ethyl-3-oxetanemethanol
- TCI D2112 97-41-6 Ethyl 2,2-Dimethyl-3-(2-methyl-1-propenyl)cyclopropane-1-carboxylate
- TCI C0595 100-49-2 Cyclohexanemethanol
- TCI P1221 24463-15-8 1-Pyrenemethanol
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- Park et al. (2019). Spectroscopic Observations of Host–Guest Hydrogen Bonding in Binary Cyclopropanemethanol + Methane Hydrate. The Journal of Physical Chemistry C doi:10.1021/acs.jpcc.9b07109
- Liu et al. (2018). Densities and Viscosities for the Ternary System of 1,2,3,4-Tetrahydronaphthalene + Isopropylcyclohexane + Cyclopropanemethanol and Corresponding Binaries at T = (293.15 to 343.15) K. Journal of Chemical & Engineering Data doi:10.1021/acs.jced.8b00662
- Jin et al. (2018). Densities and Viscosities for the Ternary System of exo-Tetrahydrodicyclopentadiene (1) + Methylcyclohexane (2) + Cyclopropanemethanol (3) and Its Binaries at T = 293.15 to 333.15 K. Journal of Chemical & Engineering Data doi:10.1021/acs.jced.8b00409
References were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.
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