4-Methoxyphenylisocyanate
4-Methoxyphenylisocyanate structure
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Common Name | 4-Methoxyphenylisocyanate | ||
|---|---|---|---|---|
| CAS Number | 5416-93-3 | Molecular Weight | 149.147 | |
| Density | 1.1±0.1 g/cm3 | Boiling Point | 221.5±23.0 °C at 760 mmHg | |
| Molecular Formula | C8H7NO2 | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | 98.3±0.0 °C | |
| Symbol |
GHS05, GHS07 |
Signal Word | 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 ... |