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1502-06-3 | Cyclodecanone
CAS No: 1502-06-3 Catalog No: AG001MEY MDL No:MFCD00003713
Product Description
Catalog Number:
AG001MEY
Chemical Name:
Cyclodecanone
CAS Number:
1502-06-3
Molecular Formula:
C10H18O
Molecular Weight:
154.2493
MDL Number:
MFCD00003713
IUPAC Name:
cyclodecanone
InChI:
InChI=1S/C10H18O/c11-10-8-6-4-2-1-3-5-7-9-10/h1-9H2
InChI Key:
SXOZDDAFVJANJP-UHFFFAOYSA-N
SMILES:
O=C1CCCCCCCCC1
EC Number:
216-119-8
UNII:
3N73MQZ9ZJ
NSC Number:
90293
Properties
Complexity:
106
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
154.136g/mol
Formal Charge:
0
Heavy Atom Count:
11
Hydrogen Bond Acceptor Count:
1
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
154.253g/mol
Monoisotopic Mass:
154.136g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
17.1A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.1
Literature
| Title | Journal |
|---|---|
| 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 20111222 |
| Structure-activity relationship for the first-in-class clinical steroid sulfatase inhibitor Irosustat (STX64, BN83495). | ChemMedChem 20111104 |
| Determination of the biologically active flavour substances thujone and camphor in foods and medicines containing sage (Salvia officinalis L.). | Chemistry Central journal 20110101 |
| Beyond the corey reaction: one-step diolefination of cyclic ketones. | The Journal of organic chemistry 20070720 |
| Thujone--cause of absinthism? | Forensic science international 20060420 |
| Total synthesis of nor-1,6-germacradien-5-ols. | The Journal of organic chemistry 20020308 |
| Reaction of arylsulfonylhydrazones of aldehydes with alpha-magnesio sulfones. A novel olefin synthesis. | The Journal of organic chemistry 20011019 |
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