54449-90-0 Usage
Molecular structure
1,2,3,4-Tetrahydro-2,4-dioxopyrrolo[1,2-a]-1,3,5-triazine-7-carboxylic acid is a heterocyclic compound with a complex chemical structure, containing a pyrrolopyrimidine derivative and a carboxylic acid functional group.
Type of compound
It is a pyrrolopyrimidine derivative, which is a type of heterocyclic compound with two or more rings containing nitrogen atoms.
Functional group
The carboxylic acid functional group (-COOH) is present in the molecule, which is known for its acidic properties and ability to form hydrogen bonds.
Potential applications
1,2,3,4-Tetrahydro-2,4-dioxopyrrolo[1,2-a]-1,3,5-triazine-7-carboxylic acid has potential applications in the field of medicinal chemistry, as it may exhibit biological activity and could be used as a building block for the synthesis of other compounds.
Structural features
The precise properties and uses of 1,2,3,4-Tetrahydro-2,4-dioxopyrrolo[1,2-a]-1,3,5-triazine-7-carboxylic acid are likely to depend on its specific structural features, such as the arrangement of atoms and the presence of various functional groups.
Molecular modifications
The properties and applications of this chemical may be altered through modifications made to its molecular structure, such as the addition or removal of functional groups or changes in the arrangement of atoms within the molecule.
Check Digit Verification of cas no
The CAS Registry Mumber 54449-90-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,4,4 and 9 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 54449-90:
(7*5)+(6*4)+(5*4)+(4*4)+(3*9)+(2*9)+(1*0)=140
140 % 10 = 0
So 54449-90-0 is a valid CAS Registry Number.
54449-90-0Relevant articles and documents
Synthesis method of triazinopyrrole formic acid
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Paragraph 0024-0025; 0028-0031; 0033-0036; 0039, (2021/11/10)
The invention discloses a synthesis method of triazinopyrrole formic acid, which comprises the following specific steps: (1) by taking a compound II as a raw material, heating and reacting in concentrated sulfuric acid to obtain an intermediate III; (2) carrying out ring closing reaction on the intermediate III and ethyl bromopyruvate to obtain an intermediate IV; and (3) hydrolyzing the intermediate IV in the presence of hydrochloric acid to obtain a target product, namely the compound I. The synthesis method disclosed by the invention is simple to operate, relatively high in yield and suitable for industrial production, and enriches the obtaining way of the fused ring compound.
