4-甲氧基苯异氰酸酯
4-甲氧基苯异氰酸酯结构式
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常用名 | 4-甲氧基苯异氰酸酯 | 英文名 | 4-Methoxyphenylisocyanate |
|---|---|---|---|---|
| CAS号 | 5416-93-3 | 分子量 | 149.147 | |
| 密度 | 1.1±0.1 g/cm3 | 沸点 | 221.5±23.0 °C at 760 mmHg | |
| 分子式 | C8H7NO2 | 熔点 | N/A | |
| MSDS | 中文版 美版 | 闪点 | 98.3±0.0 °C | |
| 符号 |
GHS05, GHS07 |
信号词 | Danger |
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CO2 and Sn(II) adducts of N-heterocyclic carbenes as delayed-action catalysts for polyurethane synthesis.
Chemistry 15(13) , 3103-9, (2009) Catalytic rivals: Both CO(2)-protected tetrahydropyrimidin-2-ylidene-based N-heterocyclic carbenes (NHCs) and Sn(II)-1,3-dimesitylimidazol-2-ylidene, as well as Sn(II)-1,3-dimesitylimidazolin-2-ylidene complexes (example displayed), have been identified as tr... |
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Biradicals from Thermolysis of N-[2-(1-Alkynyl)phenyl]-N'-phenylcarbodiimides and Their Subsequent Transformations to 6H-Indolo[2,3-b]quinolines.
J. Org. Chem. 64(3) , 925-932, (1999) Thermolysis of the carbodiimide 9a in gamma-terpinene at 138 degrees C produced 2-(phenylamino)quinoline (11a, 49%) and the parent 6H-indolo[2,3-b]quinoline (14a, 16%). Apparently, 11a was produced via the biradical 10a followed by hydrogen-atom abstraction f... |
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Design, synthesis, and biological evaluation of C9- and C2-substituted pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidines as new A2A and A3 adenosine receptors antagonists.
J. Med. Chem. 46(7) , 1229-41, (2003) In the past few years, our group has been involved in the development of A(2A) and A(3) adenosine receptor antagonists which led to the synthesis of SCH58261 (5-amino-7-(2-phenylethyl)-2-(2-furyl)pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine, 61), potent an... |
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Synthesis and Enantioseparation Ability of Xylan Bisphenylcarbamate Derivatives as Chiral Stationary Phases in HPLC.
Chirality 27 , 518-22, (2015) Ten novel xylan bisphenylcarbamate derivatives bearing meta- and para-substituents on their phenyl groups were synthesized and their chiral recognition abilities were evaluated as the chiral stationary phases (CSPs) for high-performance liquid chromatography ... |