6498-02-8 Usage
Description
ETHYL 1,2,4-TRIAZINE-3-CARBOXYLATE is a chemical compound that features a triazine ring with an ethyl ester group attached to the 3-position. It is known for its role as an intermediate in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals.
Used in Pharmaceutical Industry:
ETHYL 1,2,4-TRIAZINE-3-CARBOXYLATE is used as a chemical intermediate for the development of new drugs. Its unique structure allows it to be a key component in the creation of pharmaceuticals that can address a range of health conditions.
Used in Agrochemical Industry:
In the agrochemical sector, ETHYL 1,2,4-TRIAZINE-3-CARBOXYLATE is utilized as an intermediate in the synthesis of herbicides and pesticides. Its incorporation into these products can enhance their effectiveness in controlling weeds and pests, thereby supporting agricultural productivity.
Safety Note:
It is crucial to handle ETHYL 1,2,4-TRIAZINE-3-CARBOXYLATE with care due to its potential health and environmental risks. Adhering to safety protocols and regulations is essential when working with this chemical to minimize any adverse effects.
Check Digit Verification of cas no
The CAS Registry Mumber 6498-02-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,9 and 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6498-02:
(6*6)+(5*4)+(4*9)+(3*8)+(2*0)+(1*2)=118
118 % 10 = 8
So 6498-02-8 is a valid CAS Registry Number.
6498-02-8Relevant articles and documents
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Krass,Paudler
, p. 351 (1974)
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Synthesis of substituted fused pyridines, pyrazines and pyrimidines by sequential Ugi/inverse electron demand Diels-Alder transformations
Akritopoulou-Zanze, Irini,Wang, Ying,Zhao, Hongyu,Djuric, Stevan W.
scheme or table, p. 5773 - 5776 (2009/12/26)
The synthesis of all four regioisomers of fused pyrrolidino-pyridines in a one-pot two-step sequential Ugi-inverse electron demand Diels-Alder reaction is described. Fused pyrrolidino-pyrazines, pyrrolidino-pyrimidines and azepinone pyridines can also be obtained in consecutive synthetic sequences.
Indole as a Dienophile in Inverse Electron Demand Diels-Alder Reactions: Reactions with 1,2,4-Triazines and 1,2-Diazines
Benson, Scott C.,Gross, Jonathan L.,Snyder, John K.
, p. 3257 - 3269 (2007/10/02)
Indole reacts with 1,2,4-triazines in the absence of solvent or in the presence of limited amounts of solvent to produce β- or γ-carbolines, benzonaphthyridines, or the noncyclized 3-indoles.The combined yields of cycloadducts with tricarbalkoxytriazines exceeds 90 percent, with the production of γ-carbolines exceeding 80 percent.The regiochemistry of the adduct and the ratio of the products is determined mainly by electronic effects of the triazine substituents.Indole also ungergoes a cyclocondensation reaction with tetramethyl 1,2-diazine-3,4,5,6-tetracarboxylate to give trimethyl 5H-6-oxophenanthridine-2,3,4-tricarboxylate.