Cyclooctanone structure
|
Common Name | Cyclooctanone | ||
---|---|---|---|---|
CAS Number | 502-49-8 | Molecular Weight | 126.196 | |
Density | 0.9±0.1 g/cm3 | Boiling Point | 193.2±8.0 °C at 760 mmHg | |
Molecular Formula | C8H14O | Melting Point | 32-41 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 72.8±0.0 °C | |
Symbol |
GHS07 |
Signal Word | Warning |
Name | Cyclooctanone |
---|---|
Synonym | More Synonyms |
Density | 0.9±0.1 g/cm3 |
---|---|
Boiling Point | 193.2±8.0 °C at 760 mmHg |
Melting Point | 32-41 °C(lit.) |
Molecular Formula | C8H14O |
Molecular Weight | 126.196 |
Flash Point | 72.8±0.0 °C |
Exact Mass | 126.104462 |
PSA | 17.07000 |
LogP | 1.89 |
Vapour Pressure | 0.5±0.4 mmHg at 25°C |
Index of Refraction | 1.448 |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
|
Symbol |
GHS07 |
---|---|
Signal Word | Warning |
Hazard Statements | H315-H319-H335 |
Precautionary Statements | P261-P305 + P351 + P338 |
Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
Hazard Codes | C:Corrosive; |
Risk Phrases | R34 |
Safety Phrases | S45-S36/37/39-S26 |
RIDADR | 1325.0 |
WGK Germany | 3 |
RTECS | GX9800000 |
Hazard Class | 4.1 |
HS Code | 2914299000 |
Precursor 9 | |
---|---|
DownStream 10 | |
HS Code | 2914299000 |
---|---|
Summary | 2914299000. other cyclanic, cyclenic or cyclotherpenic ketones without other oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0% |
Rh(I)-catalyzed intramolecular [3 + 2] cycloaddition of trans-vinylcyclopropane-enes.
J. Am. Chem. Soc. 130(23) , 7178-9, (2008) Vinylcyclopropane (VCP) has been well applied as a five-carbon component, rather than a three-carbon component, in transition-metal catalyzed cycloadditions. Here we demonstrate a Rh(I)-catalyzed [3 +... |
|
Total synthesis of (+/-)-asteriscanolide.
J. Org. Chem. 66(22) , 7443-8, (2001) The total synthesis of asteriscanolide (1) has been achieved by taking advantage on an intermolecular Pauson-Khand cycloaddition and a ring-closing metathesis as key bond-forming transformations. The ... |
|
Synthesis and antimicrobial evaluation of some new cyclooctanones and cyclooctane-based heterocycles.
Arch. Pharm. (Weinheim) 345(3) , 231-9, (2012) The versatile synthon (E)-2-((dimethyl amino)methylene)cyclooctanone (2) was used as a key intermediate for the synthesis of cyclooctanones and cyclooctane-based heterocycles with pyrazole, isoxazole,... |
EINECS 207-940-2 |
MFCD00001754 |
Cyclooctanone |
cyclooctan-1-one |