Cyclodecanone - CAS 1502-06-3
Catalog: |
BB010502 |
Product Name: |
Cyclodecanone |
CAS: |
1502-06-3 |
Synonyms: |
cyclodecanone |
IUPAC Name: | cyclodecanone |
Description: | Cyclodecanone (CAS# 1502-06-3) is a useful research chemical. |
Molecular Weight: | 154.25 |
Molecular Formula: | C10H18O |
Canonical SMILES: | C1CCCCC(=O)CCCC1 |
InChI: | InChI=1S/C10H18O/c11-10-8-6-4-2-1-3-5-7-9-10/h1-9H2 |
InChI Key: | SXOZDDAFVJANJP-UHFFFAOYSA-N |
Boiling Point: | 106-107 °C / 12 mmHg (lit.) |
Density: | 0.886 g/cm3 |
Appearance: | Solid |
MDL: | MFCD00003713 |
LogP: | 3.08000 |
GHS Hazard Statement: | H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation] |
Precautionary Statement: | P264, P280, P305+P351+P338, and P337+P313 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
CN-113461504-A | Method for preparing macrocyclic alkanone from epoxide | 20210813 |
JP-2021046434-A | A new method for producing a perfluoroalkylating agent using monohydroperfluoroalkane as a starting material, and a method for producing an aromatic perfluoroalkyl compound using them. | 20201207 |
JP-2021054833-A | A new method for producing a perfluoroalkylating agent using monohydroperfluoroalkane as a starting material, and a method for producing an aromatic perfluoroalkyl compound using them. | 20201207 |
JP-2021054834-A | A new method for producing a perfluoroalkylating agent using monohydroperfluoroalkane as a starting material, and a method for producing an aromatic perfluoroalkyl compound using them. | 20201207 |
CN-112479925-A | Large naphthenone ammoximation method | 20201130 |
PMID | Publication Date | Title | Journal |
22128790 | 20111222 | Reactions of OH radicals with C6-C10 cycloalkanes in the presence of NO: isomerization of C7-C10 cycloalkoxy radicals | The journal of physical chemistry. A |
21990014 | 20111104 | Structure-activity relationship for the first-in-class clinical steroid sulfatase inhibitor Irosustat (STX64, BN83495) | ChemMedChem |
21777420 | 20110721 | Determination of the biologically active flavour substances thujone and camphor in foods and medicines containing sage (Salvia officinalis L.) | Chemistry Central journal |
17580903 | 20070720 | Beyond the corey reaction: one-step diolefination of cyclic ketones | The Journal of organic chemistry |
15896935 | 20060420 | Thujone--cause of absinthism? | Forensic science international |
Complexity: | 106 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 154.135765193 |
Formal Charge: | 0 |
Heavy Atom Count: | 11 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 154.135765193 |
Rotatable Bond Count: | 0 |
Topological Polar Surface Area: | 17.1 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 3.1 |
Online Inquiry
Customer Support
Customer Centered
Related Functional Groups
Carbonyl Compounds
Customers Also Viewed
-
[1271-47-2]
Ethynylferrocene
-
[6315-52-2]
Ethylene di(p-toluenesulfonate)
-
[1007504-11-1]
1H-Pyrazole-4-methanol, -α-,1,3,5-tetramethyl-
-
[132182-92-4]
Pentane, 1,1,1,2,2,3,4,5,5,5-decafluoro-3-methoxy-4-(trifluoromethyl)-
-
[104517-96-6]
Ioversol related compound B
-
[279-23-2]
Norbornane
INDUSTRY LEADERS TRUST OUR PRODUCTS