(Trifluoromethyl)trimethylsilane__

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1 Kilogram	Negotiable

1 Kilogram

Negotiable

Min.Order :1 Kilogram
Purity: 98%
Payment Terms : L/C,D/A,D/P,T/T,,MoneyGram

Keywords

(Trifluoromethyl)trimethylsilane RUPPERT'S REAGENT;TFMTMS;TMS-CF3;TRIMETHYL(TRIFLUOROMETHYL)SILANE;(TRIMETHYLSILYL)TRIFLUOROMETHANE;(TRIFLUOROMETHYL)TRIMETHYLSILANE;TTMS;(Trifluoromethyl)-trimethylsilan 81290-20-2

Quick Details

Appearance:clear colorless solution
Application:81290-20-2
PackAge:bottle/drum or customer's request
ProductionCapacity:1|Metric Ton|Month
Storage:N/A
Transportation:--

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Details:

(Trifluoromethyl)trimethylsilane Basic information

Product Name:	(Trifluoromethyl)trimethylsilane
Synonyms:	RUPPERT'S REAGENT;TFMTMS;TMS-CF3;TRIMETHYL(TRIFLUOROMETHYL)SILANE;(TRIMETHYLSILYL)TRIFLUOROMETHANE;(TRIFLUOROMETHYL)TRIMETHYLSILANE;TTMS;(Trifluoromethyl)-trimethylsilan
CAS:	81290-20-2
MF:	C4H9F3Si
MW:	142.19
EINECS:
Product Categories:	Fluorinated Building Blocks;Fluorinating Reagents & Building Blocks for Fluorinated Biochemical Compounds;Si (Classes of Silicon Compounds);Si-(C)4 Compounds;Silicon Compounds (for Synthesis);Synthetic Organic Chemistry;organosilicon compounds;C-C Bond Formation;Chemical Synthesis;Fluorination Reagents;Organometallic Reagents;Organosilicon;Others;Synthetic Reagents;Trifluoromethylation;Ruppert's Reagent
Mol File:	81290-20-2.mol

(Trifluoromethyl)trimethylsilane Chemical Properties

bp	54-55 °C(lit.)
density	0.962 g/mL at 20 °C(lit.)
vapor pressure	10.98 psi ( 55 °C)
refractive index	n20/D 1.386
Fp	14 °F
storage temp.	2-8°C
Sensitive	Moisture Sensitive
Merck	9683
BRN	4241868
CAS DataBase Reference	81290-20-2(CAS DataBase Reference)

Safety Information

Hazard Codes	F,Xi,Xn
Risk Statements	11-36/37-19-36/37/38-22
Safety Statements	16-33-39-26-36-29
RIDADR	UN 1993 3/PG 2
WGK Germany	3
F	10-21
Hazard Note	Flammable
TSCA	No
HazardClass	3
PackingGroup	II

(Trifluoromethyl)trimethylsilane Usage And Synthesis

Chemical Properties	clear colorless solution
Usage	Nucleophilic addition of the trifluoromethyl group to aldehydes and ketones.1

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