N-Phenylbis(trifluoromethanesulfonimide) CAS 37595-74-7 Puritas >99.0% (HPLC) Factory

Description:

Name: N-Phenylbis(trifluoromethane-sulfonimide)

Synonyma: N, N-Bis (trifluoromethylsulfonyl) aniline

CAS: 37595-74-7

Puritas: >99.0% (HPLC)

Aspectus: Alba et lux Yellow pulveris

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 N-Phenylbis(trifluoromethanesulfonimide) (CAS: 37595-74-7) with high quality, commercial production. We can provide COA, worldwide delivery, small and bulk quantities available. Please contact: alvin@ruifuchem.com

Chemical Properties:

Nomen chemicum N-Phenylbis(trifluoromethanesulfonimide)
Synonyma N-Phenyl-Bis(trifluoromethanesulfonimide);N, N-Bis(trifluoromethylsulfonyl)aniline;Phenyl Triflimide;N-Phenyltrifluoromethanesulfonimide
CAS Number 37595-74-7
CATTUS Number RF-PI1941
Stock Status In Stock, Productio Ascendite ad Tons
Formulae hypotheticae C8H5F6NO4S2
M. Pondus 357.25
Solubilitas Solutum in Methanol.Leviter solutum in Chloroforme et Ethyl acetate
Brand Ruifu Chemical

Specifications:

Item Specifications
Aspectus Alba ad lux Yellow pulveris
Puritas / Analysis Methodus >99.0% (HPLC)
Liquescens punctum 1000~102.0℃
Humor (KF) <0.20%
Totalis immunditias <1.00%
Infrared Imaginis Conformat ut Structure
Solubilitas in Ether Hyalina est lux flavus, clarus, X% est appellatus
Test Standard Enterprise Standard
Consuetudinem Prunus persica;Sulfonylation Reagentia

Sarcina & Repono:

sarcina: Utrem, aluminium foil, sacculum, 25kg/cardboard Drum, vel secundum exigentiam emptoris

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

commoda:

1

FAQ:

Applicatio:

N-Phenylbis (trifluoromethanesulfonimide) (CAS: 37595-74-7), triflans reagens, una est e reagentibus sulfonylationibus perfluoroalkyl vulgo adhibitis, vulgo in sulfonylatione hydroxyli, amino et enol perfluoroalkyl adhibita, cum magna reactivitate et selectiva optima.Ponitur in synthesi enantioselectiva aba-amino acida per reactionem Mannich.Usus in synthesi sphingosine 1-phosphate-1 receptoris agonistae usui l in applicatione pharmaceutica.Usus est nuper ad ketonam ad triflandum enol cum KHMDS convertendum, et inde olefin cum Pd(PPh3)4 et Bu3SnH.Adhibetur ut intermedium pharmaceuticum et ut medium OLED.Agit ut diaphanum validum electronicum recedens p-typum dopant in nanotubes carbonis Reactant pro: Synthesis alpha-boryl amphoterici aldehydes;Enantioselectiva synthesis nuclei anuli sceleti leucosceptroidum AD;Stereoselective synthesis of monoamine reuptake inhibitor NS9544 acetatis;Sulfoxidatio stereoselectiva.

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