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2-(2-chlorophenyl)-3-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)-1,3-thiazolidin-4-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

128317-46-4

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128317-46-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128317-46-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,3,1 and 7 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 128317-46:
(8*1)+(7*2)+(6*8)+(5*3)+(4*1)+(3*7)+(2*4)+(1*6)=124
124 % 10 = 4
So 128317-46-4 is a valid CAS Registry Number.

128317-46-4Downstream Products

128317-46-4Relevant academic research and scientific papers

Activated fly ash catalyzing the synthesis of novel potent 4-thiazolidinones of 4-amino antipyrine anils using CEM discover microwave methodology and their virtual screening

Shanti, Manoj Dilip,Shanti, Kaveri,Meshram, Jyotsana

, p. 1351 - 1360 (2013/10/08)

Fly ash, an industrial waste, has been used as an efficient and cost-effective activating catalyst for the synthesis of new potent thiazolidinones (4a-n), starting from imine (3a-n) and thioacetic acid. The reactions were performed under CEM Discover micr

Synthesis and antimicrobial activity of some 4-thiazolidinones

Trivedi, G. S.,Desai, N. C.

, p. 366 - 369 (2007/10/02)

4-Thiazolidinones have been prepared by the reaction of mercaptoacetic acids with anils or with aldehydes and amines.The structures of some of the 4-thiazolidinones (III-V) have been established on the basis of their elemental analyses and spectral data.T

Synthesis and pharmacological screening of a new series of 3-(4-antipyryl)-2-arylthiazolidin-4-ones

Al-Khamees, Hamad A.,Bayomi, Said M.,Kandil, Hesham A.,El-Tahir, Kamal E. H.

, p. 103 - 106 (2007/10/02)

A series of 3-(4-antipyryl)-2-arylthiazolidin-4-one derivatives were synthesized and pharmacologically evaluated for antinociceptive, spasmolytic and cardiovascular activities.The presence of a methoxy-naphthyl or a substituted phenyl group in 2-position

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