Cas 1246095-89-5,N-(4-{4-butoxy-3,5-bis-[4-(ethoxyoxalyl-amino)-phenylethynyl]-phenylethynyl}-phenyl)-oxalamic acid ethyl ester

1246095-89-5

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Basic information

Product Name: N-(4-{4-butoxy-3,5-bis-[4-(ethoxyoxalyl-amino)-phenylethynyl]-phenylethynyl}-phenyl)-oxalamic acid ethyl ester
Synonyms:
CAS NO:1246095-89-5
Molecular Formula:
Molecular Weight: 795.846
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: N-(4-{4-butoxy-3,5-bis-[4-(ethoxyoxalyl-amino)-phenylethynyl]-phenylethynyl}-phenyl)-oxalamic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: N-(4-{4-butoxy-3,5-bis-[4-(ethoxyoxalyl-amino)-phenylethynyl]-phenylethynyl}-phenyl)-oxalamic acid ethyl ester(1246095-89-5)
EPA Substance Registry System: N-(4-{4-butoxy-3,5-bis-[4-(ethoxyoxalyl-amino)-phenylethynyl]-phenylethynyl}-phenyl)-oxalamic acid ethyl ester(1246095-89-5)

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: 1246095-89-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1246095-89-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,6,0,9 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1246095-89:
(9*1)+(8*2)+(7*4)+(6*6)+(5*0)+(4*9)+(3*5)+(2*8)+(1*9)=165
165 % 10 = 5
So 1246095-89-5 is a valid CAS Registry Number.

1246095-89-5Upstream product

1246095-90-8 4-ethynylphenylamino oxoacetate ethyl ester

1246095-89-5Downstream Products

1246095-89-5Relevant academic research and scientific papers

Synthesis and characterization of new mono-, bis-, and tris-oxamato proligands

Stroh, Christophe,Stuparu, Alexandrina

, p. 5157 - 5159 (2010)

This communication presents the synthesis and the characterization of new organic molecules bearing up to three N-phenyl-oxalamic acid ethyl esters. The syntheses are based on Sonogashira-type cross-coupling reactions with preformed oxalamic ester interme

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