Methyl Trifluoromethanesulfonate CAS 333-27-7 Puritas >99.0% (GC) Factory

Description:

Nomen chemicum: Methyl Trifluoromethanesulfonate

CAS: 333-27-7

Puritas: >99.0% (GC)

Aspectus: Hyalina Transparens Liquid

High Quality, Commercial Production

E-Mail: alvin@ruifuchem.com


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Descriptio:

Shanghai Ruifu Chemical Co., Ltd. is the leading manufacturer and supplier of Methyl Trifluoromethanesulfonate (CAS: 333-27-7) with high quality. We can provide COA, worldwide delivery, small and bulk quantities available. Please contact: alvin@ruifuchem.com

Chemical Properties:

Nomen chemicum Methyl Trifluoromethanesulfonate
Synonyma Methyl Triflate;Trifluoromethanesulfonic Acidum Methyl Ester
CAS Number 333-27-7
CATTUS Number RF-PI2095
Stock Status In Stock, Productio Ascendite ad Tons
Formulae hypotheticae C2H3F3O3S
M. Pondus 164.10
Ferveret 94.0~99.0℃(lit.)
Density 1.45 g/mL ad 25℃(lit.)
Sensibilitas umorem Sensitivum
Brand Ruifu Chemical

Specifications:

Item Specifications
Aspectus Hyalina Transparens Liquid
Puritas / Analysis Methodus >99.0% (GC)
Index refractivus n20/D 1.324~1.328
Infrared Imaginis Conformat ut Structure
Test Standard Enterprise Standard

Sarcina & Repono:

sarcina: Utrem, 25kg/ferrum, vel secundum exigentiam emptoris

Repono Condition:Repone in vasis signatis in loco frigido et sicco;Protege a lumine et humore

commoda:

1

FAQ:

Applicatio:

Methyl Trifluoromethanesulfonate (CAS: 333-27-7) adhibetur ut potens methylating reagens in chemia.Ponitur autem in ammonium yl ammonium triflantibus conversione.Praeterea etiam usus est in reactione Suzuki.Acidum trifluoromethanesulfonicum methyl valde utile est acidum trifluoromethanesulfonicum ester reagens in synthesi organica, saepe alkylatione gerens adhibita.Trifluoromethanesulfonica estensor compositorum trifluoromethanesulfonici estens validam electronicam absorptionem facultatem habent, reactivitatem quam reagentia conventionalem alkylationem tam quam chlorinum vel alkylum sulfonate multo altiorem.Ob altitudinem activitatis suae, solum acidum trifluoromethansulfonicum yl relative stabile est.Ceterae acidi trifluoromethanesulfonici propensiores sunt ad eliminationem, conversionem et alias motus laterales, synthesim et post-tractationem sub lenis conditionibus requirunt.Synthesis organica, synthesis pharmaceutica intermedia.

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