Cas 928339-97-3,(+/-)-2-((Z)-5-benzylidene-4-oxo-2-thioxothiazolidin-3-yl)-3-phenylpropanoic acid

928339-97-3

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Basic information

Product Name: (+/-)-2-((Z)-5-benzylidene-4-oxo-2-thioxothiazolidin-3-yl)-3-phenylpropanoic acid
Synonyms: (+/-)-2-((Z)-5-benzylidene-4-oxo-2-thioxothiazolidin-3-yl)-3-phenylpropanoic acid
CAS NO:928339-97-3
Molecular Formula:
Molecular Weight: 369.465
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-((Z)-5-benzylidene-4-oxo-2-thioxothiazolidin-3-yl)-3-phenylpropanoic acid(CAS DataBase Reference)
NIST Chemistry Reference: (+/-)-2-((Z)-5-benzylidene-4-oxo-2-thioxothiazolidin-3-yl)-3-phenylpropanoic acid(928339-97-3)
EPA Substance Registry System: (+/-)-2-((Z)-5-benzylidene-4-oxo-2-thioxothiazolidin-3-yl)-3-phenylpropanoic acid(928339-97-3)

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: 928339-97-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 928339-97-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,8,3,3 and 9 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 928339-97:
(8*9)+(7*2)+(6*8)+(5*3)+(4*3)+(3*9)+(2*9)+(1*7)=213
213 % 10 = 3
So 928339-97-3 is a valid CAS Registry Number.

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928339-97-3Relevant academic research and scientific papers

Discovery of novel glitazones incorporated with phenylalanine and tyrosine: Synthesis, antidiabetic activity and structure-activity relationships

Prashantha Kumar,Baig, Nasir R.,Sudhir, Sai,Kar, Koyal,Kiranmai,Pankaj,Joghee, Nanjan M.

, p. 12 - 28 (2012)

We report a series of new glitazones incorporated with phenylalanine and tyrosine. All the compounds were tested for their in vitro glucose uptake activity using rat-hemidiaphragm, both in presence and absence of insulin. Six of the most active compounds

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