Cas 328271-98-3,5-(4-hydroxy-3-methoxybenzylidene)-3-(4-methylphenyl)-2-[(4-methylphenyl)imino]-1,3-thiazolidin-4-one

328271-98-3

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Basic information

Product Name: 5-(4-hydroxy-3-methoxybenzylidene)-3-(4-methylphenyl)-2-[(4-methylphenyl)imino]-1,3-thiazolidin-4-one
Synonyms: 5-(4-hydroxy-3-methoxybenzylidene)-3-(4-methylphenyl)-2-[(4-methylphenyl)imino]-1,3-thiazolidin-4-one
CAS NO:328271-98-3
Molecular Formula: C25H22N2O3S
Molecular Weight: 430.51878
EINECS: N/A
Product Categories: N/A
Mol File: 328271-98-3.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 5-(4-hydroxy-3-methoxybenzylidene)-3-(4-methylphenyl)-2-[(4-methylphenyl)imino]-1,3-thiazolidin-4-one(CAS DataBase Reference)
NIST Chemistry Reference: 5-(4-hydroxy-3-methoxybenzylidene)-3-(4-methylphenyl)-2-[(4-methylphenyl)imino]-1,3-thiazolidin-4-one(328271-98-3)
EPA Substance Registry System: 5-(4-hydroxy-3-methoxybenzylidene)-3-(4-methylphenyl)-2-[(4-methylphenyl)imino]-1,3-thiazolidin-4-one(328271-98-3)

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: 328271-98-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 328271-98-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,8,2,7 and 1 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 328271-98:
(8*3)+(7*2)+(6*8)+(5*2)+(4*7)+(3*1)+(2*9)+(1*8)=153
153 % 10 = 3
So 328271-98-3 is a valid CAS Registry Number.

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328271-98-3Relevant academic research and scientific papers

Synthesis and biological evaluation of pyrido-[1,2-a] pyrimidine and isoxazoline derivatives

Merja,Joshi,Parikh,Parikh

, p. 909 - 912 (2007/10/03)

Pyrido [1,2-a] pyrimidine 3a-n and isoxazoline derivatives 4a-n have been synthesized by the condensation of different arylidenes with 2-aminopyridine and hydroxylamine hydrochloride respectively. All the compounds have been characterized using spectral techniques and screened for their antimicrobial activity against several microbes.

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