Cas 1196068-60-6,N-trifluoroacetyl-2-[1-amino-2-(benzyloxy)ethyl]-1,4-naphthoquinone

1196068-60-6

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Basic information

Product Name: N-trifluoroacetyl-2-[1-amino-2-(benzyloxy)ethyl]-1,4-naphthoquinone
Synonyms: N-trifluoroacetyl-2-[1-amino-2-(benzyloxy)ethyl]-1,4-naphthoquinone
CAS NO:1196068-60-6
Molecular Formula:
Molecular Weight: 403.358
EINECS: N/A
Product Categories: N/A
Mol File: 1196068-60-6.mol
Article Data: 1

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: N-trifluoroacetyl-2-[1-amino-2-(benzyloxy)ethyl]-1,4-naphthoquinone(CAS DataBase Reference)
NIST Chemistry Reference: N-trifluoroacetyl-2-[1-amino-2-(benzyloxy)ethyl]-1,4-naphthoquinone(1196068-60-6)
EPA Substance Registry System: N-trifluoroacetyl-2-[1-amino-2-(benzyloxy)ethyl]-1,4-naphthoquinone(1196068-60-6)

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: 1196068-60-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1196068-60-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,6,0,6 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1196068-60:
(9*1)+(8*1)+(7*9)+(6*6)+(5*0)+(4*6)+(3*8)+(2*6)+(1*0)=176
176 % 10 = 6
So 1196068-60-6 is a valid CAS Registry Number.

1196068-60-6Upstream product

1196068-60-6Downstream Products

1196068-60-6Relevant articles and documents

A new synthesis of benzo [f]|isoindole-4,9-diones by radical alkylation and bromomethylation of 1,4-naphthoquinones

Deblander, Jurgen,Van Aeken, Sam,Jacobs, Jan,De Kimpe, Norbert,Tehrani, Kourosch Abbaspour

experimental part, p. 4882 - 4892 (2010/02/16)

Two synthetic routes towards substituted benzo[f]isoindole-4,9-diones have been developed. One strategy relies on the synthesis of N-trifluoroacetyl- protected 2-(l-aminoalkyl)-1,4-naphthoquinones starting from 1,4-naphthoquinone and N-trifluoroacetyl-a-a

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