2-Methylcyclopentanone - CAS 1120-72-5
Catalog: |
BB002865 |
Product Name: |
2-Methylcyclopentanone |
CAS: |
1120-72-5 |
Synonyms: |
2-methylcyclopentan-1-one |
IUPAC Name: | 2-methylcyclopentan-1-one |
Description: | 2-Methylcyclopentanone (CAS# 1120-72-5) is a useful synthetic intermediate. It was used in the synthesis of MK-0354, a partial agonist of nicotinic acid and G-protein-coupled receptor 109a. It can also be used to prepare Falcipain inhibitors. |
Molecular Weight: | 98.14 |
Molecular Formula: | C6H10O |
Canonical SMILES: | CC1CCCC1=O |
InChI: | InChI=1S/C6H10O/c1-5-3-2-4-6(5)7/h5H,2-4H2,1H3 |
InChI Key: | ZIXLDMFVRPABBX-UHFFFAOYSA-N |
Boiling Point: | 139-140 °C |
Melting Point: | -75 °C |
Purity: | 98.5 % |
Density: | 0.916 g/cm3 |
Appearance: | Colorless liquid |
Storage: | Flammables area |
MDL: | MFCD00001414 |
LogP: | 1.37550 |
GHS Hazard Statement: | H226 (100%): Flammable liquid and vapor [Warning Flammable liquids] |
Precautionary Statement: | P210, P233, P240, P241, P242, P243, P280, P303+P361+P353, P370+P378, P403+P235, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
CN-113292525-A | Preparation method of delta caprolactone | 20210616 |
CN-113429273-A | Synthesis method of metconazole intermediate | 20210609 |
CN-113214655-A | Electromagnetic shielding wave-absorbing heat-conducting film | 20210525 |
CN-113248441-A | Dual-functional ionic liquid, preparation method thereof and application thereof in catalytic synthesis of bisphenol compound | 20210430 |
CN-113185390-A | Method for continuously separating propylene glycol methyl ether, cyclopentanone and propylene glycol methyl ether acetate | 20210407 |
PMID | Publication Date | Title | Journal |
22239945 | 20120401 | Estrone direct photolysis: by-product identification using LC-Q-TOF | Chemosphere |
22059014 | 20110901 | (E)-2-Methyl-5-(thiophen-2-ylmethyl-idene)cyclopentan-1-one | Acta crystallographica. Section E, Structure reports online |
21232941 | 20110301 | Bioreduction of α,β-unsaturated ketones and aldehydes by non-conventional yeast (NCY) whole-cells | Bioresource technology |
19655736 | 20090903 | Intramolecular cyclopropene-furan [2 + 4] cycloaddition followed by a cyclopropylcarbinyl rearrangement to synthesize the BCD rings of cortistatin A | Organic letters |
19360806 | 20090504 | Insights into sequence-activity relationships amongst Baeyer-Villiger monooxygenases as revealed by the intragenomic complement of enzymes from Rhodococcus jostii RHA1 | Chembiochem : a European journal of chemical biology |
Complexity: | 86.2 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 98.073164938 |
Formal Charge: | 0 |
Heavy Atom Count: | 7 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 98.073164938 |
Rotatable Bond Count: | 0 |
Topological Polar Surface Area: | 17.1 Å2 |
Undefined Atom Stereocenter Count: | 1 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 1 |
Online Inquiry
Customer Support
Customer Centered
Related Functional Groups
Carbonyl Compounds
Customers Also Viewed
INDUSTRY LEADERS TRUST OUR PRODUCTS