89549-92-8 Usage
Purity level
96% purity
Chemical class
Pyrimidine derivative
Functional group
Carboxaldehyde
Structural features
Two methyl groups
One methylamino group
Two oxo groups
Tetrahydropyrimidine ring
Applications
Pharmaceutical and chemical synthesis
Reactivity
High reactivity due to the presence of various functional groups
Derivatives
Can form various derivatives with different functional groups
Solubility
Soluble in polar solvents such as water, methanol, and ethanol
Stability
Stable under normal laboratory conditions, but sensitive to strong acids and bases
Safety precautions
Handle with care, as it may be toxic or harmful if inhaled, ingested, or absorbed through the skin. Wear appropriate personal protective equipment (PPE) such as gloves, goggles, and lab coats when handling this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 89549-92-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,5,4 and 9 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 89549-92:
(7*8)+(6*9)+(5*5)+(4*4)+(3*9)+(2*9)+(1*2)=198
198 % 10 = 8
So 89549-92-8 is a valid CAS Registry Number.
89549-92-8Relevant articles and documents
Pyrimidine Derivatives and Related Compounds. XLVI. Thermal and Photochemical Transformation of 5-Substituted 6-Azido-1,3-dimethyluracils into Fused Pyrimidines such as Isoxazolopyrimidines, Pyrazolo-pyrimidines, and Pyrimido-t
Hirota, Kosaku,Maruhashi, Kazuo,Asao, Tetsuji,Kitamura, Norihiko,Maki, Yoshifumi,Senda, Shigeo
, p. 3959 - 3966 (2007/10/02)
Thermolysis and photolysis of 6-azido-1,3-dimethyluracils possessing certain substituents (formyl, benzoyl, hydrazonomethyl, phenyl, and benzyl groups) at the 5-position provided new methods for the preparation of fused pyrimidines.Irradiation and heating
