Cas 1233344-22-3,(Z)-5-[(4-phenylphenyl)methylidene]-3-(3,3,3-trifluoro-2-oxopropyl)-2,4-thiazolidinedione

1233344-22-3

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Basic information

Product Name: (Z)-5-[(4-phenylphenyl)methylidene]-3-(3,3,3-trifluoro-2-oxopropyl)-2,4-thiazolidinedione
Synonyms:
CAS NO:1233344-22-3
Molecular Formula:
Molecular Weight: 391.37
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: (Z)-5-[(4-phenylphenyl)methylidene]-3-(3,3,3-trifluoro-2-oxopropyl)-2,4-thiazolidinedione(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-5-[(4-phenylphenyl)methylidene]-3-(3,3,3-trifluoro-2-oxopropyl)-2,4-thiazolidinedione(1233344-22-3)
EPA Substance Registry System: (Z)-5-[(4-phenylphenyl)methylidene]-3-(3,3,3-trifluoro-2-oxopropyl)-2,4-thiazolidinedione(1233344-22-3)

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: 1233344-22-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1233344-22-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,3,3,4 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1233344-22:
(9*1)+(8*2)+(7*3)+(6*3)+(5*3)+(4*4)+(3*4)+(2*2)+(1*2)=113
113 % 10 = 3
So 1233344-22-3 is a valid CAS Registry Number.

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1233344-22-3Relevant academic research and scientific papers

Identification of new non-carboxylic acid containing inhibitors of aldose reductase

Maccari, Rosanna,Ciurleo, Rosella,Giglio, Marco,Cappiello, Mario,Moschini, Roberta,Corso, Antonella Del,Mura, Umberto,Ottanà, Rosaria

experimental part, p. 4049 - 4055 (2010/08/06)

Non-carboxylic acid containing bioisosteres of (5-arylidene-2,4-dioxothiazolidin-3-yl)acetic acids, which are active as aldose reductase (ALR2) inhibitors, were designed by replacing the carboxylic group with the trifluoromethyl ketone moiety. The in vitr

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