Cas 100796-68-7,1,3-DIMETHYL-5-[(2-PHENYLHYDRAZINO)METHYLENE]-2,4,6(1H,3H,5H)-PYRIMIDINETRIONE

100796-68-7

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Basic information

Product Name: 1,3-DIMETHYL-5-[(2-PHENYLHYDRAZINO)METHYLENE]-2,4,6(1H,3H,5H)-PYRIMIDINETRIONE
Synonyms: 1,3-DIMETHYL-5-[(2-PHENYLHYDRAZINO)METHYLENE]-2,4,6(1H,3H,5H)-PYRIMIDINETRIONE;1,3-dimethyl-5-[(2-phenylhydrazin-1-yl)methylidene]-1,3-diazinane-2,4,6-trione
CAS NO:100796-68-7
Molecular Formula: C₁₃H₁₄N₄O₃
Molecular Weight: 274.28
EINECS: N/A
Product Categories: N/A
Mol File: 100796-68-7.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: 1,3-DIMETHYL-5-[(2-PHENYLHYDRAZINO)METHYLENE]-2,4,6(1H,3H,5H)-PYRIMIDINETRIONE(CAS DataBase Reference)
NIST Chemistry Reference: 1,3-DIMETHYL-5-[(2-PHENYLHYDRAZINO)METHYLENE]-2,4,6(1H,3H,5H)-PYRIMIDINETRIONE(100796-68-7)
EPA Substance Registry System: 1,3-DIMETHYL-5-[(2-PHENYLHYDRAZINO)METHYLENE]-2,4,6(1H,3H,5H)-PYRIMIDINETRIONE(100796-68-7)

Safety Data

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Safety Statements: N/A
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RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 100796-68-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 100796-68-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,7,9 and 6 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 100796-68:
(8*1)+(7*0)+(6*0)+(5*7)+(4*9)+(3*6)+(2*6)+(1*8)=117
117 % 10 = 7
So 100796-68-7 is a valid CAS Registry Number.

100796-68-7Upstream product

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100796-68-7Relevant 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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