Triphenyltrithioorthoformate

[ Density]:
1.3±0.1 g/cm3

[ Boiling Point ]:
488.1±25.0 °C at 760 mmHg

[ Melting Point ]:
39-41ºC

[ Molecular Formula ]:
C₁₉H₁₆S₃

[ Molecular Weight ]:
340.525

[ Flash Point ]:
254.1±20.2 °C

[ Exact Mass ]:
340.041412

[ PSA ]:
75.90000

[ LogP ]:
6.82

[ Vapour Pressure ]:
0.0±1.2 mmHg at 25°C

[ Index of Refraction ]:
1.707

[ Storage condition ]:
0-10°C

Click to get detail MSDS

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

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

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
26-37/39

[ RIDADR ]:
UN 3335

[ WGK Germany ]:
3

[ HS Code ]:
2930909090

Click to get detail synthetic route

Precursor

DownStream

[ HS Code ]: 2930909090

[ Summary ]:
2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Thioorthoesters in the activated Pictet-Spengler cyclization. Synthesis of 1-thiosubstituted tetrahydroisoquinolines and carbon? carbon bond formation via sulfonyl iminium ions generated from N,S-sulfonyl acetals. Silveira CC, et al.

Tetrahedron Lett. 44(32) , 6137-40, (2003)

Lewis acid-catalyzed coupling reactions of allylsilanes with tris (phenylchalcogeno) methane. Synthesis of homoallylchalcogenoacetals. Silveira CC, et al.

Tetrahedron Lett. 37(34) , 6085-88, (1996)

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