Cas 1220909-85-2,2-((tetrahydro-1,3-dimethyl-2,4,6-trioxopyrimidin-5(6H)ylidene)methyl)amino-benzene-1,4-dioic acid

1220909-85-2

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Basic information

Product Name: 2-((tetrahydro-1,3-dimethyl-2,4,6-trioxopyrimidin-5(6H)ylidene)methyl)amino-benzene-1,4-dioic acid
Synonyms:
CAS NO:1220909-85-2
Molecular Formula:
Molecular Weight: 347.284
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-((tetrahydro-1,3-dimethyl-2,4,6-trioxopyrimidin-5(6H)ylidene)methyl)amino-benzene-1,4-dioic acid(CAS DataBase Reference)
NIST Chemistry Reference: 2-((tetrahydro-1,3-dimethyl-2,4,6-trioxopyrimidin-5(6H)ylidene)methyl)amino-benzene-1,4-dioic acid(1220909-85-2)
EPA Substance Registry System: 2-((tetrahydro-1,3-dimethyl-2,4,6-trioxopyrimidin-5(6H)ylidene)methyl)amino-benzene-1,4-dioic acid(1220909-85-2)

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: 1220909-85-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1220909-85-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,0,9,0 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1220909-85:
(9*1)+(8*2)+(7*2)+(6*0)+(5*9)+(4*0)+(3*9)+(2*8)+(1*5)=132
132 % 10 = 2
So 1220909-85-2 is a valid CAS Registry Number.

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1220909-85-2Relevant 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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