2,4-Dimethoxybenzylamine
2,4-Dimethoxybenzylamine structure
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Common Name | 2,4-Dimethoxybenzylamine | ||
|---|---|---|---|---|
| CAS Number | 20781-20-8 | Molecular Weight | 167.205 | |
| Density | 1.1±0.1 g/cm3 | Boiling Point | 272.4±25.0 °C at 760 mmHg | |
| Molecular Formula | C9H13NO2 | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | 128.4±30.4 °C | |
| Symbol |
GHS05 |
Signal Word | Danger | |
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Total synthesis of (-)-muraymycin D2 and its epimer.
J. Org. Chem. 75(5) , 1366-77, (2010) Full details of the first total synthesis of (-)-muraymycin (MRY) D2 and its epimer, the antibacterial nucleoside natural product, are described. Key strategic elements of the approach include the preparation of the urea dipeptide moiety found in the muraymyc... |
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Application of the Ugi reaction for the one-pot synthesis of uracil polyoxin C analogues.
J. Org. Chem. 74(13) , 4870-3, (2009) A simple, two-step synthesis of amide derivatives of uracil polyoxin C (UPOC) methyl ester using the Ugi reaction is described. The four components employed in the Ugi reaction are 2',3'-isopropylidine-protected uridine-5'-aldehyde, 2,4-dimethoxybenzylamine, ... |
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Synthesis of N-hydroxythiourea.
J. Med. Chem. 19(2) , 336-7, (1976) The synthesis of the title compound (1) was accomplished by the conversion of 2,4-dimethoxybenzylamine (2) into an isothiocyanate (3) using thiocarbonyl diimidazole. Treatment of 3 with hydroxylamine and removal of the DMB group with trifluoroacetic acid gave... |
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CCR5 antagonists as anti-HIV-1 agents. 1. Synthesis and biological evaluation of 5-oxopyrrolidine-3-carboxamide derivatives.
Chem. Pharm. Bull. 52 , 63-73, (2004) A novel lead compound, N-(3-[4-(4-fluorobenzoyl)piperidin-1-yl]propyl)-1-methyl-5-oxo-N-phenylpyrrolidine-3-carboxamide (1), was identified as a CCR5 antagonist by high-throughput screening using [(125)I]RANTES and CCR5-expressing CHO cells. The IC(50) value ... |
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Polymer-supported N-derivatized, o-linked hydroxylamine for concurrent solid-phase synthesis of diverse N-alkyl and N-H hydroxamates.
J. Comb. Chem. 8(3) , 435-9, (2006) We describe parallel/combinatorial, solid-phase, supported synthesis of diverse hydroxamates using a common intermediate, an N-derivatized, O-linked hydroxylamine. The method allows the concurrent synthesis of both N-alkyl and N-H hydroxamates and is compatib... |
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Synthesis of 5-substituted 4-O-methyl tetramates. Jones RC and Bates AD.
Tetrahedron Lett. 27(43) , 5285-5288, (1986)
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Tetrahedron Lett. 47 , 8459, (2006)
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