Name | Cyclopropyl carbinol |
Synonyms | CPMO CPC-OL CP-CARBINOL Cyclopropylmethanol cyclopropylmethanol CYCLOPROPYLMETHANOL Cyclopropanemethanol CYCLOPROPYL CARBINOL CYCLOPROPANEMETHANOL Cyclopropyl carbinol CYCLPOPROPANEMETHANOL (hydroxymethyl)cyclopropane (Hydroxymethyl)cyclopropane Cyclopropylmethanol for synthesis |
CAS | 2516-33-8 |
EINECS | 219-735-5 |
InChI | InChI=1/C4H8O/c5-3-4-1-2-4/h4-5H,1-3H2 |
InChIKey | GUDMZGLFZNLYEY-UHFFFAOYSA-N |
Molecular Formula | C4H8O |
Molar Mass | 72.11 |
Density | 0.89g/mLat 25°C(lit.) |
Melting Point | -60 °C |
Boling Point | 123-124°C738mm Hg(lit.) |
Flash Point | 95°F |
Water Solubility | miscible |
Solubility | Chloroform, Ethyl Acetate |
Vapor Presure | 6mmHg at 25°C |
Appearance | Liquid |
Specific Gravity | 0.890 |
Color | Clear colorless |
BRN | 1846846 |
pKa | 15.10±0.10(Predicted) |
Storage Condition | Flammables area |
Refractive Index | n20/D 1.431(lit.) |
Physical and Chemical Properties | Colorless liquid. |
Use | Used as a reagent for organic synthesis |
Risk Codes | R10 - Flammable R22 - Harmful if swallowed R36 - Irritating to the eyes R34 - Causes burns |
Safety Description | S16 - Keep away from sources of ignition. S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. |
UN IDs | UN 1987 3/PG 3 |
WGK Germany | 1 |
RTECS | GZ2212250 |
TSCA | Yes |
HS Code | 29061990 |
Hazard Note | Irritant |
Hazard Class | 3 |
Packing Group | III |
NIST chemical information | Information provided by: webbook.nist.gov (external link) |
EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
Uses | Hydroxymethyl cyclopropane is used to improve the selectivity of the phosphodiesterase 3(PDE3) inhibitor pyridine cyclooctoline phosphodiesterase 10A. It is also used to synthesize benzodiazepin-2-one. Used as an organic synthesis reagent |
Production method | It is prepared by reacting allyl alcohol with diazomethane or with diiodomethane and zinc copper couple. |