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

Short Description:

Name: N-Phenylbis(trifluoromethanesulfonimide)

Synonyms: N,N-Bis(trifluoromethylsulfonyl)aniline

CAS: 37595-74-7

Purity: >99.0% (HPLC)

Appearance: White to Light Yellow Powder

High Quality, Commercial Production

E-Mail: alvin@ruifuchem.com

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Product Detail

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Description:

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:

Chemical Name	N-Phenylbis(trifluoromethanesulfonimide)
Synonyms	N-Phenyl-Bis(trifluoromethanesulfonimide); N,N-Bis(trifluoromethylsulfonyl)aniline; Phenyl Triflimide; N-Phenyltrifluoromethanesulfonimide
CAS Number	37595-74-7
CAT Number	RF-PI1941
Stock Status	In Stock, Production Scale Up to Tons
Molecular Formula	C8H5F6NO4S2
Molecular Weight	357.25
Solubility	Soluble in Methanol. Slightly Soluble in Chloroform and Ethyl Acetate
Brand	Ruifu Chemical

Specifications:

Item	Specifications
Appearance	White to Light Yellow Powder
Purity / Analysis Method	>99.0% (HPLC)
Melting Point	100.0~102.0℃
Moisture (K.F)	<0.20%
Total Impurities	<1.00%
Infrared Spectrum	Conforms to Structure
Solubility in Ether	Colorless to Light Yellow, Clear, 10% Pass
Test Standard	Enterprise Standard
Usage	Triflating Reagent; Sulfonylation Reagents

Package & Storage:

Package: Bottle, Aluminium foil bag, 25kg/Cardboard Drum, or according to customer's requirement

Storage Condition: Store in sealed containers at cool and dry place; Protect from light and moisture

Advantages:

FAQ:

Application:

N-Phenylbis(trifluoromethanesulfonimide) (CAS: 37595-74-7), triflating reagent, is one of the commonly used perfluoroalkyl sulfonylation reagents, generally used in the perfluoroalkyl sulfonylation of phenolic hydroxyl, amino and enol, with high reactivity and excellent selectivity. It is used in the enantioselective synthesis of β-amino acids via the Mannich reaction. Used in the synthesis of sphingosine 1-phosphate-1 receptor agonists usefu l in pharmaceutical application. Employed recently to convert a ketone to an enol triflate with KHMDS and thence an olefin with Pd(PPh3)4 and Bu3SnH. Used as a pharmaceutical intermediate and as an OLED intermediate. Acts as a transparent strong electron-withdrawing p-type dopant in carbon nanotubes Reactant for: Synthesis of amphoteric alpha-boryl aldehydes; Enantioselective synthesis of core ring skeleton of leucosceptroids A-D; Stereoselective synthesis of monoamine reuptake inhibitor NS9544 acetate; Stereoselective sulfoxidation.