Cas 1254255-03-2,ethyl 3-amino-4-(p-chlorophenyl)-6-(2',3',4'-trimethoxyphenyl)-thieno[2,3-b]pyridine-2-carboxylate

1254255-03-2

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Basic information

Product Name: ethyl 3-amino-4-(p-chlorophenyl)-6-(2',3',4'-trimethoxyphenyl)-thieno[2,3-b]pyridine-2-carboxylate
Synonyms:
CAS NO:1254255-03-2
Molecular Formula:
Molecular Weight: 498.987
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: ethyl 3-amino-4-(p-chlorophenyl)-6-(2',3',4'-trimethoxyphenyl)-thieno[2,3-b]pyridine-2-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 3-amino-4-(p-chlorophenyl)-6-(2',3',4'-trimethoxyphenyl)-thieno[2,3-b]pyridine-2-carboxylate(1254255-03-2)
EPA Substance Registry System: ethyl 3-amino-4-(p-chlorophenyl)-6-(2',3',4'-trimethoxyphenyl)-thieno[2,3-b]pyridine-2-carboxylate(1254255-03-2)

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: 1254255-03-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1254255-03-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,4,2,5 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1254255-03:
(9*1)+(8*2)+(7*5)+(6*4)+(5*2)+(4*5)+(3*5)+(2*0)+(1*3)=132
132 % 10 = 2
So 1254255-03-2 is a valid CAS Registry Number.

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1254255-03-2Relevant academic research and scientific papers

Synthesis and antioxidant activity of new pyridines containing gallate moieties

El-Ebiary, Nora M. A.,Swellem, Randa H.,Mossa, Abdel-Tawab H.,Nawwar, Galal A. M.

, p. 528 - 534 (2011/05/06)

Pyridines containing the galloyl moiety have been prepared utilizing 4-acetyl pyrogallol. In addition, fused pyridines were synthesized from the obtained pyridines via further chemical transformations. The results indicated that compound 4a showed stronge

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