4271-96-9 1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine

4271-96-9 1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine Introduction

We are a pharmaceutical intermediate manufacturer of 1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine.

Its CAS No. is 4271-95-9

Our pharmaceutical intermediates can be used in a variety of APIs such as Articaine, Pyrantel, Bicalutamide, etc.

4271-96-9 1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine Specifications

4271-96-9 1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine PDF

4271-96-9 1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine.pdf

4271-96-9 1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine Factory display

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4271-96-9 1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine Certification

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4271-96-9 1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine FAQ

1. Manufacturer or trading company for 4271-96-9 1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine?

1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine is produced by EASTFINE , and we are in charge of overseas selling . Not just trading compamy .

2. 4271-96-9 1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine supplier and factories or wholesale locates in such countries like?

China,America,Brazil,England,Russia,Poland,India,Pakistan,NewZealand,Korea,Australia,Dubai,Turkey,Indonesia,UAE.

3. Can I get a sample for trying 4271-96-9 1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine?

yes , you can have 1 1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine sample for starting the business , but it is not free

4. What the MOQ of 4271-96-9 1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine?

please contact sale team for detail .

5.What are the potential applications of 4271-96-9 1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine?

Organic Synthesis: This compound can serve as an intermediate in organic synthesis, especially for the preparation of more complex heterocyclic compounds or pharmaceuticals. Its structure makes it versatile for modification and incorporation into larger molecules.

Pharmaceuticals and Medicinal Chemistry: Pyrimidine derivatives, especially those with methyl groups, have biological significance. This compound could serve as a starting material for the synthesis of antiviral, anticancer, or antibacterial agents. Many nucleoside analogs (used as antiviral drugs) are derived from pyrimidine-like structures.

Catalysis: Pyrimidine derivatives often exhibit basic properties due to the lone pairs of electrons on the nitrogen atoms. This could make 1,2-dimethyl-1,4,5,6-tetrahydropyrimidine useful as a ligand in coordination chemistry or as a catalyst in certain reactions.

Material Science: Some pyrimidine derivatives are used in the development of organic electronics, including OLEDs (organic light-emitting diodes) or as semiconductors. The incorporation of methyl groups can adjust the molecule's electronic properties for specific material applications.

6.What is the synthesis of 4271-96-9 1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine?

1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine can be synthesized through several synthetic routes, including:

Hydrogenation of Pyrimidine Derivatives: A common method involves the hydrogenation (reduction) of a pyrimidine ring or a precursor compound, such as 1,2-dimethylpyrimidine, under suitable conditions (e.g., using a metal catalyst like palladium on carbon).

Cyclization Reactions: The compound may also be synthesized via a cyclization reaction from an appropriate precursor, like a diamine and a carbonyl compound, in the presence of an acidic or basic catalyst.

Alkylation: In some cases, methylation reactions (e.g., using methyl iodide or dimethyl sulfate) can be employed to introduce the methyl groups at positions 1 and 2 of a pyrimidine ring.

7.How should 4271-96-9 1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine be stored?

Store in a cool, dry place: Keep the compound in a well-ventilated environment, away from heat sources, direct sunlight, and moisture.

Protect from air and moisture: Organic compounds with nitrogen atoms can sometimes be sensitive to moisture, which can lead to hydrolysis or degradation, so it should be kept in airtight containers.

Label and segregate: Store separately from oxidizing agents or strong acids to avoid unwanted reactions.

8.What are the environmental impacts of 4271-96-9 1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine?

Aquatic Toxicity: As with many nitrogen-containing organic compounds, 1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine may be toxic to aquatic life if released into water systems. Proper containment and disposal methods should be followed to minimize environmental contamination.

Persistence: The compound may persist in the environment, especially if it does not degrade easily, so care should be taken to ensure it does not accumulate.

9.How should 4271-96-9 1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine be disposed of?

Dispose of according to local hazardous waste disposal regulations. Organic compounds like 1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine should not be disposed of down the drain or in regular trash.

Neutralization or treatment may be required if the compound reacts with specific reagents or solvents. For disposal in larger quantities, consult a certified chemical waste disposal service for proper handling.

10.What reactions can 4271-96-9 1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine undergo?

Electrophilic Substitution: The nitrogen atoms in the pyrimidine ring make the compound potentially reactive in electrophilic substitution reactions.

Nucleophilic Substitution: The amino group (if present in other derivatives) can participate in nucleophilic substitution reactions, enabling the formation of more complex molecules.

Hydrogenation: The compound may undergo hydrogenation if used as a precursor for creating more saturated pyrimidine derivatives.

Cyclization and Functionalization: With proper reagents, 1,2-Dimethyl-1,4,5,6-tetrahydropyrimidine can be used as a precursor for larger cyclic compounds or undergo functionalization to introduce other substituents.