63677-40-7 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
The compound is derived from 1,2,4-triazolophthalazine-3-carboxylic acid by attaching an ethyl ester group.
Explanation
The compound has a ring structure consisting of both carbon and nitrogen atoms, making it a heterocyclic compound.
Explanation
The compound's structure may be used as a starting point for designing new drugs due to its unique ring system.
Explanation
The compound may be used as a building block for the synthesis of biologically active compounds, making it valuable in the pharmaceutical industry.
Explanation
The compound's properties and potential uses make it a subject of interest for researchers in the fields of chemistry and pharmaceuticals.
Ethyl Ester Derivative
1,2,4-triazolophthalazine-3-carboxylic acid
Heterocyclic Compound
Contains a triazolophthalazine ring system
Potential Pharmacophore
For drug design
Applications
Pharmaceutical industry
Research Interest
Chemical and pharmaceutical research
Check Digit Verification of cas no
The CAS Registry Mumber 63677-40-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,6,7 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 63677-40:
(7*6)+(6*3)+(5*6)+(4*7)+(3*7)+(2*4)+(1*0)=147
147 % 10 = 7
So 63677-40-7 is a valid CAS Registry Number.
63677-40-7Relevant articles and documents
FACTORS INFLUENCING THE PATHWAY OF REACTIONS OF 1-HYDRAZINOPHTHALAZINE WITH DI- AND TRICARBONYL COMPOUNDS
Amer, Adel,Weisz, Klaus,Zimmer, Hans
, p. 1853 - 1862 (2007/10/02)
The reaction of 1-hydrazinophthalazine (hydralazine) (1) with substituted ethyl benzoylpyruvates (3) leads under neutral reaction conditions to 3--4H-as-triazinophthalazin-4-ones (4).Under acidic but otherwise identical conditions depending on the substituent of 3, 4 and/or 3-carbethoxy-s-triazolophthalazine (5) with simultaneous elimination of the appropriate acetophenone were obtained. 1-HCl and substituted ethyl cinnamoylpyruvates (6a-e) give rise to formation of 1-(1-phthalazinyl)-3-carbethoxy-5-(3- or 4-substituted styryl)pyrazoles (7).Under neutral conditions the reaction of 1 with 6 gives as-triazinophthalazine (8).The structures of 4, 5, 7, and 8 are based on elemental analysis and extensive ms- and 1H-nmr investigations.
