185011-09-0 Usage
Chemical class
Imidazolidin-2-one derivatives
Appearance
White crystalline solid
Molecular weight
281.33 g/mol
Pharmaceutical use
Building block for the synthesis of various bioactive molecules and drug candidates
Potential applications
Anti-cancer and anti-inflammatory agent
Preclinical studies
Shown potential as an anti-cancer and anti-inflammatory agent
Unique structure
Valuable tool for drug discovery and medicinal chemistry research
Ongoing research
Full range of biological activities and potential therapeutic uses are still being investigated
Check Digit Verification of cas no
The CAS Registry Mumber 185011-09-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,0,1 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 185011-09:
(8*1)+(7*8)+(6*5)+(5*0)+(4*1)+(3*1)+(2*0)+(1*9)=110
110 % 10 = 0
So 185011-09-0 is a valid CAS Registry Number.
185011-09-0Relevant articles and documents
Reaction of 4,5-dihydroxy-2-imidazolidinones with arylsulfinic acids. Synthesis of 4-arylsulfonyl-2-imidazolinones
Shutalev,Sivova
, p. 1147 - 1151 (2007/10/03)
The reaction of 4,5-dihydroxy-2-imidazolidinones with arylsulfinic acids in water upon heating leads to 4-arylsulfonyl-2-imidazolinones. The formation of such compounds was found to proceed through the loss of a water molecule or sulfinic acid from intermediate 4-hydroxy-5-arylsulfonyl-2-imidazolidinones and 4,5-di(arylsulfonyl)-2-imidazolidinones. 4-Arylsulfonyl-2-imidazolinones are also formed upon heating glyoxal, urea, and arylsulfinic acids in water. 1997 Plenum Publishing Corporation.