102284-74-2 Usage
Chemical class
Diaminopyrimidines It belongs to a group of chemical compounds that contain two amino groups attached to a pyrimidine ring.
Molecular structure
Two allyl groups and two amino groups attached to a uracil ring This unique structure contributes to its various applications in the polymer industry and potential uses in biotechnology and medicine.
Potential applications
Biotechnology and medicine Due to its ability to interact with nucleic acids and proteins, it may have uses in these fields, although further research is needed to explore these possibilities.
Hydrochloride form
Commonly used for stability and solubility The hydrochloride salt form of the compound is preferred in various applications because it provides better stability and solubility in different solvents, making it easier to work with in chemical reactions and formulations.
Solubility
Soluble in water and some organic solvents This property allows for easy handling and incorporation into various formulations, both in the polymer industry and potentially in biotechnological and pharmaceutical applications.
Molecular weight
Approximately 248.7 g/mol This value is useful for determining the concentration of the compound in various solutions and for calculating reaction stoichiometry.
Appearance
White to off-white crystalline solid This physical form makes it suitable for handling, storage, and incorporation into different applications.
Check Digit Verification of cas no
The CAS Registry Mumber 102284-74-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,2,8 and 4 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 102284-74:
(8*1)+(7*0)+(6*2)+(5*2)+(4*8)+(3*4)+(2*7)+(1*4)=92
92 % 10 = 2
So 102284-74-2 is a valid CAS Registry Number.
102284-74-2Relevant articles and documents
8-substituted xanthines as selective adenosine receptor agents
-
, (2008/06/13)
Xanthine derivatives having general structure (I) including the (R) and (S) enantiomers and racemic mixtures thereof, and the pharmaceutically acceptable salts thereof, wherein R 1 and R 2 are each independently (C 1 -C 4)lower alkyl or (C 2 -C 4)lower al
XANTHINE DERIVATIVES AS ADENOSINE A1 RECEPTOR ANTAGONISTS
-
, (2008/06/13)
A method of attenuating a cognitive deficit in a patient in need thereof comprising administering to the patient a xanthine derivative.
Selective adenosine receptor agents
-
, (2008/06/13)
Xanthine derivative which act selectively at adenosine receptors and which act in general as adenosine antagonists are disclosed. From in vitro studies it is known that specific physiological effects can be distinguished as a result of this selectively and that adenosine receptor activity in vitro correlates with adenosine receptor activity in vivo.Pharmaceutical preparations of the subject compounds can be prepared on the basis of the selective binding activity of the compounds disclosed herein which will enhance certain physiological effects while minimizing others, such as decreasing blood pressure without decreasing heart rate.
Analogue of Coffeine and Theophylline: Effect of Structural Alterations on Affinity at Adenosine Receptors
Daly, J. W.,Padgett, W. L.,Shamim, M. T.
, p. 1305 - 1308 (2007/10/02)
A variety of analogues of caffeine and theophylline in which the 1-, 3-, and 7-methyl substituents have been replaced with n-propyl, allyl, propargyl, and isobutyl and, in few cases with chloroethyl, hydroxyethyl, or benzyl were assessed for potency and s
