Cas no 21032-48-4 (2-(dimethylsilyl)pyridine)
2-(dimethylsilyl)pyridine Chemical and Physical Properties
Names and Identifiers
-
- 2-(dimethylsilyl)pyridine
- 2-(DIMETHYLSILY)PYRIDINE
- dimethyl(pyridin-2-yl)silicon
- (2-pyridyl)Me2SiH
- 2-(3-NITRO-PHENYL)-7-TRIFLUOROMETHYL-IMIDAZO[1,2-A]PYRIDINE
- 2-(dimethylhydrosilyl)pyridine
- 2-dimethylsilanyl-pyridine
- 2-pyridyldimethylsilane
- Dimethyl(2-pyridyl)silane
- dimethylpyridylsilane
- Pyridine,2-(dimethylsilyl)
- MFCD06797091
- QNRXNPHFYDOLOT-UHFFFAOYSA-N
- starbld0044758
- 2-(Dimethylsilyl)pyridine, 90%
- 21032-48-4
- Pyridine, 2-(dimethylsilyl)-
- SCHEMBL3973497
- DTXSID60476626
- AKOS015840029
-
- MDL: MFCD06797091
- Inchi: 1S/C7H10NSi/c1-9(2)7-5-3-4-6-8-7/h3-6H,1-2H3
- InChI Key: QNRXNPHFYDOLOT-UHFFFAOYSA-N
- SMILES: [Si](C)(C)C1C=CC=CN=1 |^1:0|
Computed Properties
- Exact Mass: 137.06600
- Monoisotopic Mass: 136.058250858g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 9
- Rotatable Bond Count: 1
- Complexity: 83
- 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
- Surface Charge: 0
- Tautomer Count: nothing
- XLogP3: nothing
- Topological Polar Surface Area: 12.9?2
Experimental Properties
- Color/Form: {"from":"zh","to":"en","trans_result":[{"src":"\u672a\u786e\u5b9a","dst":"Not determined"},{"src":"2.\u00a0\u5bc6\u5ea6\uff08g\/mL,25\/4\u2103\uff09","dst":"2. density (g\/ml, 25\/4 \u2103)"}]}
- Density: 0.915?g/mL?at 25?°C
- Flash Point: Fahrenheit: 104 ° f
Celsius: 40 ° c - Refractive Index: n20/D 1.499
- PSA: 12.89000
- LogP: 0.77530
2-(dimethylsilyl)pyridine Security Information
-
Symbol:
- Signal Word:Warning
- Hazard Statement: H226-H315-H319-H335
- Warning Statement: P261-P305+P351+P338
- Hazardous Material transportation number:UN 1993 3/PG 3
- WGK Germany:3
- Hazard Category Code: 10-36/37/38
- Safety Instruction: 26-36
-
Hazardous Material Identification:
- Storage Condition:2-8°C
2-(dimethylsilyl)pyridine Customs Data
- HS CODE:2933399090
- Customs Data:
China Customs Code:
2933399090Overview:
2933399090. Other compounds with non fused pyridine rings in 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:
2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
2-(dimethylsilyl)pyridine Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| XI GE MA AO DE LI QI ( SHANG HAI ) MAO YI Co., Ltd. | 681490-1G |
2-(dimethylsilyl)pyridine |
21032-48-4 | 1g |
¥1480.72 | 2023-11-29 | ||
| SHENG KE LU SI SHENG WU JI SHU | sc-251672-1 g |
2-(Dimethylsilyl)pyridine, |
21032-48-4 | 1g |
¥1,241.00 | 2023-07-11 | ||
| SHENG KE LU SI SHENG WU JI SHU | sc-251672-1g |
2-(Dimethylsilyl)pyridine, |
21032-48-4 | 1g |
¥1241.00 | 2023-09-05 |
2-(dimethylsilyl)pyridine Related Literature
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Zhiyan Chen,Nan Wu,Yaobing Wang,Bing Wang,Yingde Wang J. Mater. Chem. A, 2018,6, 516-526
-
Ana G. Neo,Ana Bornadiego,Jesús Díaz,Stefano Marcaccini,Carlos F. Marcos Org. Biomol. Chem., 2013,11, 6546-6555
-
Yukiya Kitayama Polym. Chem., 2014,5, 2784-2792
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Shintaro Takata,Yoshihiro Miura Phys. Chem. Chem. Phys., 2014,16, 24784-24789
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Eric Besson,Stéphane Gastaldi,Emily Bloch,Selma Aslan,Hakim Karoui,Olivier Ouari,Micael Hardy Analyst, 2019,144, 4194-4203
Additional information on 2-(dimethylsilyl)pyridine
Introduction to 2-(Dimethylsilyl)Pyridine (CAS No: 21032-48-4)
2-(Dimethylsilyl)pyridine is a versatile organic compound with the CAS number 21032-48-4, which has garnered significant attention in the fields of organic synthesis, catalysis, and materials science. This compound is a silylated derivative of pyridine, where a dimethylsilyl group (-SiMe?) is attached to the second position of the pyridine ring. The unique combination of the electron-withdrawing pyridine ring and the electron-donating silyl group makes this compound highly reactive and functional, enabling its use in various chemical transformations and applications.
The synthesis of 2-(dimethylsilyl)pyridine involves the reaction of pyridine with dimethylchlorosilane (Me?SiCl) in the presence of a base, typically under reflux conditions. This reaction is straightforward and has been optimized for high yields, making it accessible for both academic and industrial purposes. The compound's structure is characterized by its aromatic pyridine ring, which imparts stability and reactivity, while the dimethylsilyl group introduces silicon-based functionality that can be exploited in various chemical reactions.
One of the most notable applications of 2-(dimethylsilyl)pyridine is its use as a precursor in the synthesis of silylated heterocycles. These derivatives are valuable in organic chemistry due to their ability to participate in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, where they serve as effective ligands or catalysts. Recent studies have highlighted the role of silylated pyridine derivatives in enhancing the selectivity and efficiency of these reactions, making them indispensable in modern synthetic methodologies.
In addition to its role in organic synthesis, 2-(dimethylsilyl)pyridine has found applications in materials science. The compound's ability to form stable complexes with transition metals has led to its use in catalytic systems for polymerization reactions. For instance, it has been employed as a co-catalyst in olefin polymerization processes, where it significantly improves the catalytic activity and product quality. This application underscores the importance of silicon-containing heterocycles in advancing polymer chemistry.
The electronic properties of 2-(dimethylsilyl)pyridine also make it a promising candidate for use in electronic materials. Research has shown that this compound can be incorporated into conjugated systems to modulate their electronic characteristics, which is crucial for applications in organic electronics such as light-emitting diodes (LEDs) and photovoltaic devices. The integration of silicon-based heterocycles into these systems offers new possibilities for enhancing device performance and efficiency.
Recent advancements in green chemistry have also explored the use of 2-(dimethylsilyl)pyridine as an environmentally friendly alternative to traditional organometallic reagents. Its ability to function under mild reaction conditions reduces energy consumption and waste generation, aligning with sustainable chemical practices. This shift towards greener synthesis methods highlights the growing importance of silicon-containing compounds in contemporary chemical research.
In conclusion, 2-(dimethylsilyl)pyridine (CAS No: 21032-48-4) is a multifaceted compound with diverse applications across organic synthesis, catalysis, materials science, and electronics. Its unique structure and reactivity continue to drive innovative research, positioning it as a key player in advancing modern chemistry.
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