Cas 1374161-71-3,2-amino-4-(benzo[d][1,3]dioxol-5-yl)-8-chloro-3-(4-chlorobenzoyl)-1-phenyl-1H-thiochromeno[2,3-b]pyridin-5(4H)-one

1374161-71-3

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Basic information

Product Name: 2-amino-4-(benzo[d][1,3]dioxol-5-yl)-8-chloro-3-(4-chlorobenzoyl)-1-phenyl-1H-thiochromeno[2,3-b]pyridin-5(4H)-one
Synonyms:
CAS NO:1374161-71-3
Molecular Formula:
Molecular Weight: 599.494
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-amino-4-(benzo[d][1,3]dioxol-5-yl)-8-chloro-3-(4-chlorobenzoyl)-1-phenyl-1H-thiochromeno[2,3-b]pyridin-5(4H)-one(CAS DataBase Reference)
NIST Chemistry Reference: 2-amino-4-(benzo[d][1,3]dioxol-5-yl)-8-chloro-3-(4-chlorobenzoyl)-1-phenyl-1H-thiochromeno[2,3-b]pyridin-5(4H)-one(1374161-71-3)
EPA Substance Registry System: 2-amino-4-(benzo[d][1,3]dioxol-5-yl)-8-chloro-3-(4-chlorobenzoyl)-1-phenyl-1H-thiochromeno[2,3-b]pyridin-5(4H)-one(1374161-71-3)

Safety Data

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Safety Statements: N/A
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RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1374161-71-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1374161-71-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,4,1,6 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1374161-71:
(9*1)+(8*3)+(7*7)+(6*4)+(5*1)+(4*6)+(3*1)+(2*7)+(1*1)=153
153 % 10 = 3
So 1374161-71-3 is a valid CAS Registry Number.

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1374161-71-3Relevant academic research and scientific papers

Modulating the reactivity of functionalized N,S-ketene acetal in MCR: Selective synthesis of tetrahydropyridines and thiochromeno[2,3-b]pyridines via DABCO-catalyzed tandem annulation

Wen, Li-Rong,Shi, Yong-Jie,Liu, Guang-Yuan,Li, Ming

, p. 4252 - 4260 (2012)

An efficient and straightforward three-component synthetic protocol was developed to synthesize 1,2,3,4-tetrahydropyridine derivatives or thiochromeno[2,3-b]pyridine derivatives from β-aroylthioacetanilides or β-(2-haloaroyl)thioacetanilides, aldehydes, a

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