Cas 897960-96-2,2-(4-fluorophenyl)-2-(4,6-dimethyl-2-hydroxyphenyl)-N-(4-methylphenylsulfonyl)-ethanamine

897960-96-2

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Basic information

Product Name: 2-(4-fluorophenyl)-2-(4,6-dimethyl-2-hydroxyphenyl)-N-(4-methylphenylsulfonyl)-ethanamine
Synonyms: 2-(4-fluorophenyl)-2-(4,6-dimethyl-2-hydroxyphenyl)-N-(4-methylphenylsulfonyl)-ethanamine
CAS NO:897960-96-2
Molecular Formula:
Molecular Weight: 413.513
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: 2-(4-fluorophenyl)-2-(4,6-dimethyl-2-hydroxyphenyl)-N-(4-methylphenylsulfonyl)-ethanamine(CAS DataBase Reference)
NIST Chemistry Reference: 2-(4-fluorophenyl)-2-(4,6-dimethyl-2-hydroxyphenyl)-N-(4-methylphenylsulfonyl)-ethanamine(897960-96-2)
EPA Substance Registry System: 2-(4-fluorophenyl)-2-(4,6-dimethyl-2-hydroxyphenyl)-N-(4-methylphenylsulfonyl)-ethanamine(897960-96-2)

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: 897960-96-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 897960-96-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,7,9,6 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 897960-96:
(8*8)+(7*9)+(6*7)+(5*9)+(4*6)+(3*0)+(2*9)+(1*6)=262
262 % 10 = 2
So 897960-96-2 is a valid CAS Registry Number.

897960-96-2Upstream product

897960-96-2Downstream Products

897960-96-2Relevant academic research and scientific papers

Facile regio- and stereoselective carbon-carbon coupling of phenol derivatives with aryl aziridines

Pineschi, Mauro,Bertolini, Ferruccio,Crotti, Paolo,Macchia, Franco

, p. 2627 - 2630 (2007/10/03)

A chemo-, regio-, and stereoselective direct carbon-carbon coupling of readily available aryl borates with N-protected aryl aziridines provides a method for the synthesis of new 2-(o-hydroxyaryl)-2-aryl ethylamines which can be used, in a novel annulation

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