Cas 1361254-17-2,[2-(10-oxo-9-phenylethynyl-2,3,5,6-tetrahydro-1H,4H-11-oxa-3a-aza-benzo[de]anthracen-8-yl)ethyl]carbamic acid benzyl ester

1361254-17-2

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Basic information

Product Name: [2-(10-oxo-9-phenylethynyl-2,3,5,6-tetrahydro-1H,4H-11-oxa-3a-aza-benzo[de]anthracen-8-yl)ethyl]carbamic acid benzyl ester
Synonyms: [2-(10-oxo-9-phenylethynyl-2,3,5,6-tetrahydro-1H,4H-11-oxa-3a-aza-benzo[de]anthracen-8-yl)ethyl]carbamic acid benzyl ester
CAS NO:1361254-17-2
Molecular Formula:
Molecular Weight: 518.612
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-(10-oxo-9-phenylethynyl-2,3,5,6-tetrahydro-1H,4H-11-oxa-3a-aza-benzo[de]anthracen-8-yl)ethyl]carbamic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [2-(10-oxo-9-phenylethynyl-2,3,5,6-tetrahydro-1H,4H-11-oxa-3a-aza-benzo[de]anthracen-8-yl)ethyl]carbamic acid benzyl ester(1361254-17-2)
EPA Substance Registry System: [2-(10-oxo-9-phenylethynyl-2,3,5,6-tetrahydro-1H,4H-11-oxa-3a-aza-benzo[de]anthracen-8-yl)ethyl]carbamic acid benzyl ester(1361254-17-2)

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: 1361254-17-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1361254-17-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,1,2,5 and 4 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1361254-17:
(9*1)+(8*3)+(7*6)+(6*1)+(5*2)+(4*5)+(3*4)+(2*1)+(1*7)=132
132 % 10 = 2
So 1361254-17-2 is a valid CAS Registry Number.

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1361254-17-2Relevant academic research and scientific papers

A mild titanium-catalyzed synthesis of functionalized amino coumarins as fluorescence labels

Wirtz, Lisa,Kazmaier, Uli

, p. 7062 - 7065 (2012/01/05)

In contrast to Bronsted and other Lewis acids ClTi(OiPr)3 is especially suited to catalyze the formation of amino-substituted coumarins from aminophenols and functionalized β-oxo esters in a Pechmann condensation. This straightforward protocol allows the synthesis of fluorescence labels and false fluorescent neurotransmitters.

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