Cas 1334682-23-3,trifluoromethanesulfonic acid 2-[2-(4-fluorophenyl)-2-oxo-acetylamido]phenyl ester

1334682-23-3

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Basic information

Product Name: trifluoromethanesulfonic acid 2-[2-(4-fluorophenyl)-2-oxo-acetylamido]phenyl ester
Synonyms: trifluoromethanesulfonic acid 2-[2-(4-fluorophenyl)-2-oxo-acetylamido]phenyl ester
CAS NO:1334682-23-3
Molecular Formula:
Molecular Weight: 391.3
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: trifluoromethanesulfonic acid 2-[2-(4-fluorophenyl)-2-oxo-acetylamido]phenyl ester(CAS DataBase Reference)
NIST Chemistry Reference: trifluoromethanesulfonic acid 2-[2-(4-fluorophenyl)-2-oxo-acetylamido]phenyl ester(1334682-23-3)
EPA Substance Registry System: trifluoromethanesulfonic acid 2-[2-(4-fluorophenyl)-2-oxo-acetylamido]phenyl ester(1334682-23-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1334682-23-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1334682-23-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,4,6,8 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1334682-23:
(9*1)+(8*3)+(7*3)+(6*4)+(5*6)+(4*8)+(3*2)+(2*2)+(1*3)=153
153 % 10 = 3
So 1334682-23-3 is a valid CAS Registry Number.

1334682-23-3Upstream product

1334682-23-3Downstream Products

1334682-45-9 (R)-3-(4-fluorophenyl)-3-hydroxyoxindole

1334682-23-3Relevant academic research and scientific papers

A facile pathway to enantiomerically enriched 3-hydroxy-2-oxindoles: Asymmetric intramolecular arylation of α-keto amides catalyzed by a palladium-DifluorPhos complex

Yin, Liang,Kanai, Motomu,Shibasaki, Masakatsu

, p. 7620 - 7623 (2011/09/30)

Less metal wastes: The first catalytic, enantioselective intramolecular aryl-transfer reaction of aryl triflates to ketones has been developed (see scheme; R1=R2=aromatic and aliphatic). This method features overall practicality, inc

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