Cas 224957-17-9,{4-acetyl-6-oxo-3-phenyl-5-[(5-trifluoromethyl-benzothiazol-2-ylmethyl)-amino]-6<i>H</i>-pyridazin-1-yl}-acetic acid ethyl ester

224957-17-9

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Basic information

Product Name: {4-acetyl-6-oxo-3-phenyl-5-[(5-trifluoromethyl-benzothiazol-2-ylmethyl)-amino]-6H-pyridazin-1-yl}-acetic acid ethyl ester
Synonyms: {4-acetyl-6-oxo-3-phenyl-5-[(5-trifluoromethyl-benzothiazol-2-ylmethyl)-amino]-6H-pyridazin-1-yl}-acetic acid ethyl ester
CAS NO:224957-17-9
Molecular Formula:
Molecular Weight: 530.527
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-acetyl-6-oxo-3-phenyl-5-[(5-trifluoromethyl-benzothiazol-2-ylmethyl)-amino]-6H-pyridazin-1-yl}-acetic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: {4-acetyl-6-oxo-3-phenyl-5-[(5-trifluoromethyl-benzothiazol-2-ylmethyl)-amino]-6H-pyridazin-1-yl}-acetic acid ethyl ester(224957-17-9)
EPA Substance Registry System: {4-acetyl-6-oxo-3-phenyl-5-[(5-trifluoromethyl-benzothiazol-2-ylmethyl)-amino]-6H-pyridazin-1-yl}-acetic acid ethyl ester(224957-17-9)

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HazardClass: N/A
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Hazardous Substances Data: 224957-17-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 224957-17-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,4,9,5 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 224957-17:
(8*2)+(7*2)+(6*4)+(5*9)+(4*5)+(3*7)+(2*1)+(1*7)=149
149 % 10 = 9
So 224957-17-9 is a valid CAS Registry Number.

224957-17-9Upstream product

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224957-17-9Relevant academic research and scientific papers

Isoxazolo-[3,4-d]-pyridazin-7-(6H)-one as a potential substrate for new aldose reductase inhibitors

Costantino, Luca,Rastelli, Giulio,Gamberini, M. Cristina,Giovannoni, M. Paola,Piaz, Vittorio Dal,Vianello, Paola,Barlocco, Daniela

, p. 1894 - 1900 (2007/10/03)

The isoxazolo-[3,4-d]-pyridazin-7-(6H)-one (2) and its corresponding open derivatives 5-acetyl-4-amino-(4-nitro)-6-substituted-3(2H)pyridazinones (3, 4) were used as simplified substrates for the synthesis of new aldose reductase inhibitors with respect t

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