Cas 353284-24-9,5-[(2-hydroxyanilino)methylene]-1,3-dimethyl-2,4,6(1H,3H,5H)-pyrimidinetrione

353284-24-9

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Basic information

Product Name: 5-[(2-hydroxyanilino)methylene]-1,3-dimethyl-2,4,6(1H,3H,5H)-pyrimidinetrione
Synonyms: 5-[(2-hydroxyanilino)methylene]-1,3-dimethyl-2,4,6(1H,3H,5H)-pyrimidinetrione
CAS NO:353284-24-9
Molecular Formula: C₁₃H₁₃N₃O₄
Molecular Weight: 275.26002
EINECS: N/A
Product Categories: N/A
Mol File: 353284-24-9.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-[(2-hydroxyanilino)methylene]-1,3-dimethyl-2,4,6(1H,3H,5H)-pyrimidinetrione(CAS DataBase Reference)
NIST Chemistry Reference: 5-[(2-hydroxyanilino)methylene]-1,3-dimethyl-2,4,6(1H,3H,5H)-pyrimidinetrione(353284-24-9)
EPA Substance Registry System: 5-[(2-hydroxyanilino)methylene]-1,3-dimethyl-2,4,6(1H,3H,5H)-pyrimidinetrione(353284-24-9)

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: 353284-24-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 353284-24-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,3,2,8 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 353284-24:
(8*3)+(7*5)+(6*3)+(5*2)+(4*8)+(3*4)+(2*2)+(1*4)=139
139 % 10 = 9
So 353284-24-9 is a valid CAS Registry Number.

353284-24-9Upstream product

353284-24-9Downstream Products

353284-24-9Relevant academic research and scientific papers

Synthesis of highly functionalized barbituric acids and study of their interactions with p-glycoprotein and Mg2+ - Potential candidates for multi drug resistance modulation

Singh, Palwinder,Kaur, Jatinder,Bhardwaj, Atul

experimental part, p. 1256 - 1262 (2010/05/02)

A number of barbituric acids with appropriate substituent at C-5 position were synthesized and investigated for their interactions with p-gp and Mg2+. Compounds 5, 6, 8-10, 12-14 and 16 increased the basal activity of p-gp by more than 50% at 0

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