TBDMS Triflate CAS 69739-34-0 Puritas > 98.0%
Shanghai Ruifu Chemical Co., Ltd. est primarius fabrica et elit tert-Butyldimethylsilyl Trifluoromethanesulfonate (CAS: 69739-34-0) cum qualitate magna.CoA praebere possumus, totius orbis partus, parvas et parvas quantitates in promptu habentes.Please contact: alvin@ruifuchem.com
Nomen chemicum | tert-Butyldimethylsilyl Trifluoromethanesulfonate |
Synonyma | Trifluoromethanesulfonic Acid tert-Butyldimethylsilylester;tert-Butyldimethylsilyl Triflate;TBDMS Triflate;TBS Triflate |
CAS Number | 69739-34-0 |
CATTUS Number | RF-PI2112 |
Stock Status | In Stock, Productio Ascendite ad Tons |
Formulae hypotheticae | C7H15F3O3SSi |
M. Pondus | 264.34 |
Ferveret | 65.0~67.0℃/12 mm Hg (lit.) |
Aqua Solubility | Decomposes |
Sensibilitas | umorem Sensitivum |
Hydrolytic Sensibilitas | 8: Raptim Reacts cum umore, aqua, protic solvendo |
Aleam Nota | Flammabiles / Corrosive |
Periculum Classis | 3 |
Stipare Group | III |
HS Code* | 29310095 |
Fasciae vita | LX Menses |
Articuli / Opuscula | Pii Compounds |
Brand | Ruifu Chemical |
Item | Specifications |
Aspectus | Hyalina ad lux Yellow Fuming Liquid |
Puritas / Analysis Methodus | > 98.0% (Titration Neutralization) |
Index refractivus n20/D | 1.384~1.388 |
Densitas (20℃) | 1.148~1.156 |
Aquae (KF) | <0.10% |
Infrared Imaginis | Conformat ut Structure |
Proton NMR Spectrum | Conformat ut Structure |
Test Standard | Enterprise Standard |
sarcina: Fluorinated Utrem, 25kg/ Ferocactus, vel secundum exigentiam elit
Repono Condition:Repone in vasis signatis in loco frigido et sicco;Protege a lumine et humore
tert-Butyldimethylsilyl Trifluoromethanesulfonate (CAS: 69739-34-0) est valde reactivum activum silylatum et acidum lewis capax convertendi alcoholos primas, secundas et tertiarias ad eorum respectivam TBDMS.TrifluoroMethanesulfonicum acidum tert-butyldiMethylsilyl niensis adhibetur etiam ad opercula ketones et lactones in aetheres eorum enol silyl.TBDMS Triflate adhibetur ut agens silylating valde reactivum et Acidum Lewis et capax convertendi alcohols1b prima, secundaria et tertiaria ad aetherem respondentem TBDMS, et ketones et lactones convertens in aetheres suos enol silyllos;promovere adiectionem conjugatarum compositorum alkynylzinci et triphenylphosphini 5 ad α, β-enones;activatio chromonum in [4+2] cycloadditionum profectae, permutatio tributylstannyllorum silyllorum aetheris allici;activum pyridini annulorum versus Grignard reagentes et transalkylationem aminis tertiarii N-oxidum; et transformatio coetus Nt-butoxycarbonyl in coetus N-alkoxycarbonyl.