Cas 1349199-99-0,(+/-)-2-((Z)-5-benzylidene-4-oxo-2-thioxothiazolidin-3-yl)-3-(4-hydroxyphenyl)propanoic acid

1349199-99-0

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Basic information

Product Name: (+/-)-2-((Z)-5-benzylidene-4-oxo-2-thioxothiazolidin-3-yl)-3-(4-hydroxyphenyl)propanoic acid
Synonyms: (+/-)-2-((Z)-5-benzylidene-4-oxo-2-thioxothiazolidin-3-yl)-3-(4-hydroxyphenyl)propanoic acid
CAS NO:1349199-99-0
Molecular Formula:
Molecular Weight: 385.464
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-(4-hydroxyphenyl)propanoic acid(CAS DataBase Reference)
NIST Chemistry Reference: (+/-)-2-((Z)-5-benzylidene-4-oxo-2-thioxothiazolidin-3-yl)-3-(4-hydroxyphenyl)propanoic acid(1349199-99-0)
EPA Substance Registry System: (+/-)-2-((Z)-5-benzylidene-4-oxo-2-thioxothiazolidin-3-yl)-3-(4-hydroxyphenyl)propanoic acid(1349199-99-0)

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: 1349199-99-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1349199-99-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,9,1,9 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1349199-99:
(9*1)+(8*3)+(7*4)+(6*9)+(5*1)+(4*9)+(3*9)+(2*9)+(1*9)=210
210 % 10 = 0
So 1349199-99-0 is a valid CAS Registry Number.

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1349199-99-0Relevant 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 (2013/01/15)

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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