Cyclopropyl methyl ketone - CAS 765-43-5
Catalog: |
BB035609 |
Product Name: |
Cyclopropyl methyl ketone |
CAS: |
765-43-5 |
Synonyms: |
1-cyclopropylethanone |
IUPAC Name: | 1-cyclopropylethanone |
Description: | Cyclopropyl methyl ketone (CAS# 765-43-5) is a chemical reagents used in the synthesis of PDE4 inhibitors. Also used in the synthesis of α-trifluoromethyl-amines. |
Molecular Weight: | 84.12 |
Molecular Formula: | C5H8O |
Canonical SMILES: | CC(=O)C1CC1 |
InChI: | InChI=1S/C5H8O/c1-4(6)5-2-3-5/h5H,2-3H2,1H3 |
InChI Key: | HVCFCNAITDHQFX-UHFFFAOYSA-N |
Boiling Point: | 114 °C |
Melting Point: | <-70°C |
Flash Point: | 21°C |
Purity: | 95 % |
Density: | 0.903 g/cm3 |
Appearance: | Clear colorless to very slightly yellow liquid |
Storage: | Flammables area |
MDL: | MFCD00001297 |
LogP: | 0.98540 |
Refractive Index: | 1.422-1.426 |
Stability: | Stable under normal temperatures and pressures. |
Vapor Pressure: | 44.7 [mmHg] |
GHS Hazard Statement: | H225 (86.36%): Highly Flammable liquid and vapor [Danger Flammable liquids] |
Precautionary Statement: | P210, P233, P240, P241, P242, P243, P264, P270, P280, P301+P310, P301+P312, P303+P361+P353, P305+P351+P338, P310, P321, P330, P337+P313, P370+P378, P403+P235, P405, and P501 |
Signal Word: | Danger |
Publication Number | Title | Priority Date |
CN-113461657-A | Organic small molecule gel and preparation method and application thereof | 20210817 |
CN-113072434-A | Method for preparing cyclopropyl methyl ketone by one-step method | 20210401 |
CN-113049712-A | Method for measuring content of cyclopropyl methyl ketone | 20210323 |
CN-113511964-A | Synthetic method of high-content 2, 2-dichloro-1- (1-chlorocyclopropyl) ethanone for quantitative and qualitative analysis | 20210318 |
CN-112851485-A | Preparation method of ticagrelor key intermediate | 20210115 |
PMID | Publication Date | Title | Journal |
22692411 | 20120701 | Male-produced sex pheromone of the stink bug Edessa meditabunda | Journal of chemical ecology |
21959804 | 20111001 | Preparation and evaluation of 5, 9-dimethyl-2-cyclopropyl-2-decanol as a penetration enhancer for drugs through rat skin | Pakistan journal of pharmaceutical sciences |
19718721 | 20091005 | Synthesis and reactivity of six-membered oxa-nickelacycles: a ring-opening reaction of cyclopropyl ketones | Chemistry (Weinheim an der Bergstrasse, Germany) |
19397271 | 20090528 | (Z)- and (E)-2-(1,2-dihydroxyethyl)methylenecyclopropane analogues of 2'-deoxyadenosine and 2'-deoxyguanosine. Synthesis of all stereoisomers, absolute configuration, and antiviral activity | Journal of medicinal chemistry |
17374172 | 20070321 | Synthesis of spiropyrans: H-abstractions in 3-cycloalkenyloxybenzopyrans | Beilstein journal of organic chemistry |
Complexity: | 72 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 84.057514874 |
Formal Charge: | 0 |
Heavy Atom Count: | 6 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 84.057514874 |
Rotatable Bond Count: | 1 |
Topological Polar Surface Area: | 17.1 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 0.5 |
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