AgrochemicalsChlorimuron-Ethyl Impurity 2
Original price was: ₹60,000.00.₹50,000.00Current price is: ₹50,000.00.
Name:2-Amino-4-chloro-6-methoxy-pyrimidine CAT. NO.:SAC-09-B CAS NO.:5734-64-5
- Description
- Datasheet
- Additional information
Description
Chlorimuron-Ethyl Impurity 2
| Chemical Name | 2-Amino-4-chloro-6-methoxy-pyrimidine |
| Catalog Number | SAC-09-B |
| Parent AI | Chlorimuron-Ethyl |
| Synonyms | 4-Chloro-6-methoxy-2-pyrimidinamine; (4-Chloro-6-methoxypyrimidin-2-yl)amine; 2-Amino-6-chloro-4-methoxypyrimidine; 4-Chloro-6-methoxy-2-pyrimidinamine; 4-Methoxy-6-chloro-2-aminopyrimidine; NSC 28420 |
| CAS Number | 5734-64-5 |
| Molecular Formula | C₅H₆ClN₃O |
| Molecular Weight | 159.57 |
| Appearance | Solid |
| Melting Point | 168-171 °C |
| Shipping & Storage Information
|
Storage-20°C
Shipping: Free Shipping at Room Temperature in INDIA, may vary elsewhere Stability: Datasheet |
| Solubility | NA |
| Stability | Air Sensitive |
| Category | Agrochemical Impurity Standard/Metabolites; |
| Description &Applications | 2-Amino-4-chloro-6-methoxypyrimidine, also known as ACMP, is an organic compound with a wide range of applications in scientific research. It is a member of the pyrimidine family, which is a heterocyclic aromatic organic compound. ACMP has been extensively studied for its potential use in the synthesis of new drugs and therapeutic agents, as well as for its potential use in biochemical and physiological studies. |
| References | Sharma, Seema., et al.: FEMS Micriobiol. Lett., 337(1), 18-24 (2012) |
2-Amino-4-chloro-6-methoxy-pyrimidine, a compound of interest due to its unique combination of functional groups and its potential for contributing to the development of novel drugs and materials.
Chemical Structure and Properties: 2-Amino-4-chloro-6-methoxy-pyrimidine is a heterocyclic compound with a pyrimidine core, which consists of a six-membered ring containing two nitrogen atoms and four carbon atoms. The presence of an amino group (-NH2) at position 2, a chlorine atom (Cl) at position 4, and a methoxy group (-OCH3) at position 6 adds specific chemical properties to the compound. These functional groups make it an interesting candidate for various synthetic and biological applications.
Synthesis and Functionalization: The synthesis of 2-Amino-4-chloro-6-methoxy-pyrimidine often involves multi-step processes. One common approach includes the reaction of a suitable precursor with appropriate reagents to introduce the amino, chloro, and methoxy substituents at the desired positions on the pyrimidine ring. Careful control of reaction conditions and purification steps is essential to ensure a high yield of the desired product.
Biological Activity: Heterocyclic compounds, especially those containing nitrogen atoms, often exhibit diverse biological activities. In the case of 2-Amino-4-chloro-6-methoxy-pyrimidine, its structural features make it a potential candidate for pharmaceutical research. The presence of an amino group can facilitate interactions with biological macromolecules, and the chloro and methoxy groups might modulate the compound’s solubility and interactions with specific target sites.
Researchers are investigating the compound’s potential as a pharmacologically active agent. It could serve as a scaffold for the design and synthesis of new drugs targeting various diseases. Initial studies might involve assessing its interactions with proteins, enzymes, or receptors to evaluate its potential as a therapeutic agent.
Applications in Materials Science: Beyond its biological applications, 2-Amino-4-chloro-6-methoxy-pyrimidine might find utility in materials science. Heterocyclic compounds are often incorporated into polymers and materials to impart specific properties. The functional groups in this pyrimidine derivative could enable it to participate in various chemical reactions for the modification of polymers, development of coatings, or production of functional materials.
Additional information
| Pack Size | 50mg |
|---|
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