1,3-Bis[3,5-bis(trifluoromethyl)phenyl]thiourea

Modify Date: 2024-01-04 19:48:50

1,3-Bis[3,5-bis(trifluoromethyl)phenyl]thiourea Structure
1,3-Bis[3,5-bis(trifluoromethyl)phenyl]thiourea structure
Common Name 1,3-Bis[3,5-bis(trifluoromethyl)phenyl]thiourea
CAS Number 1060-92-0 Molecular Weight 500.30500
Density 1.604g/cm3 Boiling Point 332.7ºC at 760 mmHg
Molecular Formula C17H8F12N2S Melting Point 152 °C
MSDS Chinese USA Flash Point 155ºC
Symbol GHS07
GHS07
Signal Word Warning

 Names

Name 1,3-Bis[3,5-bis(trifluoromethyl)phenyl]thiourea
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.604g/cm3
Boiling Point 332.7ºC at 760 mmHg
Melting Point 152 °C
Molecular Formula C17H8F12N2S
Molecular Weight 500.30500
Flash Point 155ºC
Exact Mass 500.02200
PSA 63.19000
LogP 7.86420
Vapour Pressure 0.000143mmHg at 25°C
Index of Refraction 1.503

 Safety Information

Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H315-H319
Precautionary Statements P280-P305 + P351 + P338-P337 + P313
RIDADR NONH for all modes of transport

 Articles6

More Articles
Activation of a carbonyl compound by halogen bonding.

Chem. Commun. (Camb.) 50(47) , 6281-4, (2014)

Using a prototypical Diels-Alder reaction as benchmark, we show that dicationic halogen-bond donors are capable of activating a neutral organic substrate. By various comparison experiments, the action...

Trisubstituted 2-trifluoromethyl pyrrolidines via catalytic asymmetric Michael addition/reductive cyclization.

Org. Lett. 16(9) , 2362-5, (2014)

The stereoselective synthesis of trisubstituted 2-trifluoromethyl pyrrolidines by asymmetric Michael addition/hydrogenative cyclization is described. The direct organocatalytic addition of 1,1,1-trifl...

Water-compatible hydrogen-bond activation: a scalable and organocatalytic model for the stereoselective multicomponent aza-Henry reaction.

Chemistry 19(49) , 16550-4, (2013)

 Synonyms

1,3-Bis[3,5-bis(trifluoroMethyl)phenyl]thiourea
1,3-bis[3,5-bis(trifluoromethyl)phenyl]thiourea