Cas 150454-73-2,{4,6-Bis-[1-(4-chloro-phenyl)-2-oxo-ethylidene]-[1,3,5]triazinan-2-ylidene}-(4-chloro-phenyl)-acetaldehyde

150454-73-2

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Basic information

Product Name: {4,6-Bis-[1-(4-chloro-phenyl)-2-oxo-ethylidene]-[1,3,5]triazinan-2-ylidene}-(4-chloro-phenyl)-acetaldehyde
Synonyms:
CAS NO:150454-73-2
Molecular Formula:
Molecular Weight: 538.817
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: {4,6-Bis-[1-(4-chloro-phenyl)-2-oxo-ethylidene]-[1,3,5]triazinan-2-ylidene}-(4-chloro-phenyl)-acetaldehyde(CAS DataBase Reference)
NIST Chemistry Reference: {4,6-Bis-[1-(4-chloro-phenyl)-2-oxo-ethylidene]-[1,3,5]triazinan-2-ylidene}-(4-chloro-phenyl)-acetaldehyde(150454-73-2)
EPA Substance Registry System: {4,6-Bis-[1-(4-chloro-phenyl)-2-oxo-ethylidene]-[1,3,5]triazinan-2-ylidene}-(4-chloro-phenyl)-acetaldehyde(150454-73-2)

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: 150454-73-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 150454-73-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,4,5 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 150454-73:
(8*1)+(7*5)+(6*0)+(5*4)+(4*5)+(3*4)+(2*7)+(1*3)=112
112 % 10 = 2
So 150454-73-2 is a valid CAS Registry Number.

150454-73-2Upstream product

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150454-73-2Relevant academic research and scientific papers

Selective Mono, Bis, and Trisiminoformylation of 2,4,6-trialkyl-1,3,5-Triazines - Unusual Anol Acylenamine Tautomerism of Hydroxyalkenyl-1,3,5-triazines

Schulz, Hans-Joachim,Liebscher, Juergen,Luger, Peter,Quian, Minxie,Mulzer, Johann

, p. 1125 - 1132 (2007/10/02)

2,4,6-Trialkyl-1,3,5-triazines 1 can selectively be mono, bis or trisiminoformylated by reaction with trismorpholinomethane 2 or chloromethylene iminium salts 3 (Vilsmeier reagents), with each alkyl substituent reacting with only one molecule of the elect

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