CYCLOOCTANONE

CYCLOOCTANONE
  • CAS No.:502-49-8
Other grades of this product :
CYCLOOCTANONE Basic information
Product Name:CYCLOOCTANONE
Synonyms:TIMTEC-BB SBB008888;CYCLOOCTAN-1-ONE;CYCLOOCTANONE;Cyclooctanone,97%;Azelaone;Cyclooctanone,98%;Cyclooctanone, 98% 100GR;Cyclooctanone, 98% 500GR
CAS:502-49-8
MF:C8H14O
MW:126.2
EINECS:207-940-2
Product Categories:Aliphatics, Pharmaceuticals, Intermediates & Fine Chemicals;C7 to C8;Carbonyl Compounds;Ketones
Mol File:502-49-8.mol
CYCLOOCTANONE Chemical Properties
Melting point 32-41 °C (lit.)
Boiling point 195-197 °C (lit.)
density 0.958 g/mL at 25 °C (lit.)
refractive index 1.4694
Fp 163 °F
storage temp. Sealed in dry,Room Temperature
solubility 15g/l
form Crystalline Low Melting Solid
color Colorless to white
PH7 (15g/l, H2O, 20℃)
Water Solubility Soluble in water at 20°C 15g/L. Soluble in acetone, alcohol, chloroform, methanol and benzene.
BRN 1280738
InChIKeyIIRFCWANHMSDCG-UHFFFAOYSA-N
LogP2.11
CAS DataBase Reference502-49-8(CAS DataBase Reference)
EPA Substance Registry SystemCyclooctanone (502-49-8)
Safety Information
Hazard Codes C,Xi
Risk Statements 34-52/53-36/37/38
Safety Statements 45-36/37/39-26-61
RIDADR 1759
WGK Germany 3
RTECS GX9800000
TSCA Yes
HazardClass 8
HS Code 29142990
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
CYCLOOCTANONE Usage And Synthesis
Chemical Propertiescolorless to white crystalline low melting solid
UsesCyclooctanone is a aliphatic cycle that exhibited inhibitory activity towards aldosterone synthase, a promising therapeutic target for the treatment of cardiovascular diseases related to abnormally high aldosterone level.
UsesCyclooctanone is a aliphatic cycle that exhibited inhibitory activity towards aldosterone synthase, a promising therapeutic target for the treatment of cardiovascular diseases related to abnormally high aldosterone level. It is also used in the synthesis of 14-membered lactones.
Synthesis Reference(s)Journal of the American Chemical Society, 92, p. 5276, 1970 DOI: 10.1021/ja00720a078The Journal of Organic Chemistry, 49, p. 3912, 1984 DOI: 10.1021/jo00195a007Tetrahedron Letters, 36, p. 2921, 1995 DOI: 10.1016/0040-4039(95)00467-Q
Purification MethodsPurify the ketone by sublimation after drying with Linde type 13X molecular sieves. The semicarbazone has m 168-169o (from dioxane) [Kohler et al. J Am Chem Soc 61 1060 1939]. The oxime has m 36-37o after subliming at high vacuum or distillation and has b 128-129o /14mm. The iso-oxime has m 72-73o [Ruzicka et al. Helv Chim Acta 32 548 1949]. [Beilstein 7 III 77, 7 IV 49.]

Welcome!

Please leave a message for us or use the following ways to contact us, we will reply to you as soon as possible, and provide you with the most sincere service, thank you.

  • NO. 18 ,Wujiang Road, Wulidian Street, Jiangbei District, Chongqing
  • +86-23-6139-8061 +86-13650506873
  • danny@chemdad.com sales@chemdad.com
  • www.chemdad.com
  • WhatsApp +86-13650506873

Name

phone

company

email

message

Payment methods
Google translate: 日本语日本语 한국어한국어 FrançaisFrançais DeutschDeutsch EspañaEspaña TürkiyeTürkiye