Cas no 64376-14-3 (2-Amino-6-methylpyrimidine-4-carbonitrile)
2-Amino-6-methylpyrimidine-4-carbonitrile Chemical and Physical Properties
Names and Identifiers
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- 2-Amino-6-methylpyrimidine-4-carbonitrile
- 2-AMINO-4-CYANO-6-METHYLPYRIMIDINE
- 4-Pyrimidinecarbonitrile,2-amino-6-methyl-
- 2-Amino-4-methyl-6-cyan-pyrimidin
- 2-Amino-6-cyano-4-methylpyrimidin
- 2-Amino-6-methyl-pyrimidin-4-carbonitril
- 2-amino-6-methyl-pyrimidine-4-carbonitrile
- AG-664/25005969
- FT-0691540
- 64376-14-3
- DTXSID50355951
- A834736
- YXSNOFWJDHHMPD-UHFFFAOYSA-N
- AKOS006241955
- SB56005
- 2-amino-6-cyano-4-methylpyrimidine
- SCHEMBL10692686
- DB-017507
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- Inchi: 1S/C6H6N4/c1-4-2-5(3-7)10-6(8)9-4/h2H,1H3,(H2,8,9,10)
- InChI Key: YXSNOFWJDHHMPD-UHFFFAOYSA-N
- SMILES: N1C(N)=NC(C#N)=CC=1C
Computed Properties
- Exact Mass: 134.05900
- Monoisotopic Mass: 134.059246208g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 10
- Rotatable Bond Count: 0
- Complexity: 158
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 0.3
- Topological Polar Surface Area: 75.6?2
Experimental Properties
- Density: 1.27
- Boiling Point: 397.9 °C at 760 mmHg
- Flash Point: 194.5 °C
- Refractive Index: 1.582
- PSA: 75.59000
- LogP: 0.82008
2-Amino-6-methylpyrimidine-4-carbonitrile Customs Data
- HS CODE:2933599090
- Customs Data:
China Customs Code:
2933599090Overview:
2933599090. Other compounds with pyrimidine ring in structure(Including other compounds with piperazine ring on the structure. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%
Declaration elements:
Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date
Summary:
2933599090. other compounds containing a pyrimidine ring (whether or not hydrogenated) or piperazine ring in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
2-Amino-6-methylpyrimidine-4-carbonitrile Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Chemenu | CM164892-1g |
2-amino-6-methylpyrimidine-4-carbonitrile |
64376-14-3 | 95% | 1g |
$489 | 2021-08-05 | |
| Chemenu | CM164892-1g |
2-amino-6-methylpyrimidine-4-carbonitrile |
64376-14-3 | 95% | 1g |
$447 | 2023-02-17 | |
| Ambeed | A610931-1g |
2-Amino-6-methylpyrimidine-4-carbonitrile |
64376-14-3 | 95+% | 1g |
$422.0 | 2025-04-18 |
2-Amino-6-methylpyrimidine-4-carbonitrile Suppliers
2-Amino-6-methylpyrimidine-4-carbonitrile Related Literature
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Hongxia Li,Aikifa Raza,Qiaoyu Ge,Jin-You Lu,TieJun Zhang Soft Matter, 2020,16, 6841-6849
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Bin Han,Yasuo Shimizu,Gabriele Seguini,Celia Castro,Gérard Ben Assayag,Koji Inoue,Yasuyoshi Nagai,Sylvie Schamm-Chardon,Michele Perego RSC Adv., 2016,6, 3617-3622
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Weili Dai,Guangjun Wu,Michael Hunger Chem. Commun., 2015,51, 13779-13782
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Amandine Altmayer-Henzien,Valérie Declerck,David J. Aitken,Ewen Lescop,Denis Merlet,Jonathan Farjon Org. Biomol. Chem., 2013,11, 7611-7615
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Jason Y. C. Lim,Yong Yu,Guorui Jin,Kai Li,Yi Lu,Jianping Xie Nanoscale Adv., 2020,2, 3921-3932
Additional information on 2-Amino-6-methylpyrimidine-4-carbonitrile
Comprehensive Overview of 2-Amino-6-methylpyrimidine-4-carbonitrile (CAS No. 64376-14-3)
2-Amino-6-methylpyrimidine-4-carbonitrile (CAS No. 64376-14-3) is a versatile heterocyclic compound widely used in pharmaceutical and agrochemical research. This pyrimidine derivative is characterized by its amino and cyano functional groups, which make it a valuable intermediate in organic synthesis. Researchers frequently explore its applications in drug discovery, particularly in the development of kinase inhibitors and antimicrobial agents. The compound's molecular structure (C6H6N4) offers unique reactivity, enabling modifications for targeted biological activity.
In recent years, the demand for 2-Amino-6-methylpyrimidine-4-carbonitrile has surged due to its role in synthesizing small-molecule therapeutics. Its relevance in cancer research and central nervous system (CNS) drug development aligns with trending scientific inquiries, such as "how to design selective kinase inhibitors" or "novel pyrimidine-based antimicrobials." The compound's CAS No. 64376-14-3 is often searched alongside terms like "synthetic routes," "spectroscopic data," and "safety profiles," reflecting its technical importance.
From a synthetic chemistry perspective, 2-Amino-6-methylpyrimidine-4-carbonitrile serves as a precursor for multi-step reactions, including palladium-catalyzed cross-coupling and nucleophilic substitutions. Its nitrile group allows further functionalization, making it a staple in medicinal chemistry libraries. Analytical techniques like HPLC, NMR, and mass spectrometry are commonly employed to verify its purity, a topic frequently queried in academic forums.
Environmental and regulatory considerations are also critical. While not classified as hazardous, proper handling of 64376-14-3 is emphasized in laboratory safety guidelines. Users often search for "storage conditions" or "compatibility with solvents," underscoring the need for precise technical documentation. The compound's stability under various pH levels and temperatures is another area of interest, particularly for industrial-scale applications.
Innovations in green chemistry have spurred interest in sustainable synthesis methods for 2-Amino-6-methylpyrimidine-4-carbonitrile. Questions like "catalytic alternatives for pyrimidine synthesis" or "solvent-free reactions" dominate discussions in research communities. These advancements align with global trends toward eco-friendly manufacturing, further elevating the compound's profile.
In summary, 2-Amino-6-methylpyrimidine-4-carbonitrile (CAS No. 64376-14-3) remains a cornerstone in modern organic synthesis, bridging gaps between academia and industry. Its adaptability to high-throughput screening and structure-activity relationship (SAR) studies ensures its enduring relevance in solving complex biochemical challenges.
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