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1502-06-3

1502-06-3 Structure

1502-06-3 Structure
IdentificationBack Directory
[Name]

CYCLODECANONE
[CAS]

1502-06-3
[Synonyms]

NSC 90293
CYCLODECANONE
Ketocyclodecane
CYCLODECAN-1-ONE
Cyclodecanone,97%
Cyclodecanone 97%
CYCLODECANONE CRYSTALLINE
N-(6-amino-1-methyl-2,4-dioxo-5-pyrimidinyl)formamide
[EINECS(EC#)]

216-119-8
[Molecular Formula]

C10H18O
[MDL Number]

MFCD00003713
[MOL File]

1502-06-3.mol
[Molecular Weight]

154.25
Chemical PropertiesBack Directory
[Melting point ]

21-24 °C(lit.)
[Boiling point ]

106-107 °C12 mm Hg(lit.)
[density ]

0.958 g/mL at 25 °C(lit.)
[refractive index ]

n20/D 1.482(lit.)
[Fp ]

180 °F
[storage temp. ]

2-8°C
[solubility ]

Chloroform (Slightly), Methanol (Slightly)
[form ]

Colourless Oil to Semi-Solid
[BRN ]

1617127
[LogP]

2.929 (est)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36
[Safety Statements ]

26
[WGK Germany ]

3
[F ]

9-23
[HS Code ]

29142990
Hazard InformationBack Directory
[Chemical Properties]

White solid or colorless liquid
[Synthesis Reference(s)]

Journal of the American Chemical Society, 86, p. 3068, 1964 DOI: 10.1021/ja01069a019
Organic Syntheses, Coll. Vol. 4, p. 218, 1963
Synthetic Communications, 9, p. 437, 1979 DOI: 10.1080/00397917908064174
[Purification Methods]

Purify the ketone via the semicarbazone (m 205-207o, from EtOH) and distil it through an efficient column. It sublimes in a vacuum. The oxime has m 80o, from MeOH or by sublimation in a high vacuum. [Cope et al. Org Synth Coll Vol IV 218 1963, Prelog et al. Helv Chim Acta 30 1746 1947, Ruzicka et al. Helv Chim Acta 11 675 1930, Beilstein 7 III 134, 7 IV 76.]
Spectrum DetailBack Directory
[Spectrum Detail]

CYCLODECANONE(1502-06-3)MS
CYCLODECANONE(1502-06-3)1HNMR
CYCLODECANONE(1502-06-3)13CNMR
CYCLODECANONE(1502-06-3)IR1
CYCLODECANONE(1502-06-3)Raman
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