(TRIFLUOROMETHYL)TRIMETHYLSILANE

pro_cas
81290-20-2
pro_cdbregno
CCD00072385
pro_formula
C4 H9 F3 Si
pro_molWeight
142.195

basic_info

Product_Name: (TRIFLUOROMETHYL)TRIMETHYLSILANE
CAS: 81290-20-2
EnglishSynonyms: TMS-CF3 ; RUPPERT'S REAGENT ; (TRIFLUOROMETHYL)TRIMETHYLSILANE ; TTMS ; (TRIFLUOROMETHYL)-TRIMETHYLSILAN ; TFMTMS ; TRIMETHYL(TRIFLUOROMETHYL)SILANE ; RUPPERT-PRAKASH REAGENT ; (TRIMETHYLSILYL)TRIFLUOROMETHANE
pro_mdlNumber: MFCD00145454
pro_acceptors: 0
pro_donors: 0
pro_smile: C[Si](C)(C)C(F)(F)F
InChi: InChI=1S/C4H9F3Si/c1-8(2,3)4(5,6)7/h1-3H3
InChiKey: InChIKey=MWKJTNBSKNUMFN-UHFFFAOYSA-N

property

Boiling_Point: 45 DEG C/40 °C/40 °C
Density: 0.962g/mLat20°C(lit.)
PhysicalProperty: FLASHPOINT: -17 DEG C
FLASHPOINT: 1.4 DEG F
REFRACTIVE INDEX: N20/D 1.386
Comments: APPLICATION: REACTANT FOR: SILVER-MEDIATED C-H TRIFLUOROMETHYLATION OF ARENES. PREPARATION OF TRIFLUOROMETHYL KETONE ANALOG OF L-ARGININE HAVING CONTRASTING INHIBITORY ACTIVITY AGAINST HUMAN ARGINASE I AND HISTONE DEACETYLASE 82. ORGANOCATALYZED REGIO- AND ENANTIOSELECTIVE ALLYLIC TRIFLUOROMETHYLATION OF MORITA-BAYLIS-HILLMAN ADDUCTS. PALLADIUM-CATALYZED OXIDATIVE TRIFLUOROMETHYLATION OF INDOLES. PREPARATION OF 5-HT1A ANTAGONISTS. USED AS DIFLUOROCARBENE SOURCE
CONCENTRATION: APPROX 2.0 M IN THF
FORM: SOLUTION
RIDADR: UN 1993 3/PG 2
UNSPSC: 12352100
WGK: 3
Concentration: 0.5MinTHF

secure_info

secure_symbol: GHS02 GHS02
secure_signal_word: Danger
secure_risk_stmt: H225
secure_cautionary_stmt: P210
secure_damage_code: F
secure_risk_disclosure_stmt: R:11
secure_security_stmt: S:16-33
secure_un_code: 1993
secure_wgk_germany: 3

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