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FARNESAL

Names

[ CAS No. ]:
19317-11-4

[ Name ]:
FARNESAL

[Synonym ]:
10-dodecatrienal,3,7,11-trimethyl-6
3,7,11-Trimethyl-2,6,10-dodecatrienal
3,7,10-trimethyl-2,6,10-dodecatrienal
3,7,11-trimethyl-dodeca-2,6,10-trienal
Farnesal,Pract.
Einecs 242-957-9
2,6,10-Farnesatrien-1-al
FARNESAL
farnesyl aldehyde

Chemical & Physical Properties

[ Density]:
0.868g/cm3

[ Boiling Point ]:
328.6ºC at 760mmHg

[ Molecular Formula ]:
C15H24O

[ Molecular Weight ]:
220.35000

[ Flash Point ]:
147.8ºC

[ Exact Mass ]:
220.18300

[ PSA ]:
17.07000

[ LogP ]:
4.60450

[ Vapour Pressure ]:
0.000187mmHg at 25°C

[ Index of Refraction ]:
n20/D >1.4920(lit.)

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
36/37/38

[ Safety Phrases ]:
26-36

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2912190090

Customs

[ HS Code ]: 2912190090

[ Summary ]:
2912190090 acyclic aldehydes without other oxygen function。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:5.5%。General tariff:30.0%

Articles

Knockdown or inhibition of aldo-keto reductase 1B10 inhibits pancreatic carcinoma growth via modulating Kras-E-cadherin pathway.

Cancer Lett. 355(2) , 273-80, (2014)

Aldo-keto reductase 1B10 (AKR1B10) has relatively specific lipid substrates including carbonyls, retinal and farnesal/geranylgeranial. Metabolizing these lipid substrates appears crucial to carcinogen...

Formation of farnesal and 3-hydroxy-2,3-dihydrofarnesal from farnesol by protoplasts of Botryococcus braunii.

Biochem. Biophys. Res. Commun. 196(3) , 1401-5, (1993)

Farnesal and 3-hydroxy-2,3-dihydrofarnesal (3-hydroxy-3,7,11-trimethyl-6,10-dodecadiene-1-al) were formed from farnesol when the alcohol was incubated with the protoplast of Botryococcus braunii B rac...

Zeolite NaY-promoted cyclization of farnesal: a short route to nanaimoal.

J. Org. Chem. 73(7) , 2905-8, (2008)

The sesquiterpene nanaimoal was synthesized in 21% overall yield and in a biomimetic manner. As a key step, the acid-catalyzed cyclization of farnesal under zeolite NaY confinement conditions was used...


More Articles


Related Compounds

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