3-methoxybenzyl bromide
3-methoxybenzyl bromide structure
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Common Name | 3-methoxybenzyl bromide | ||
|---|---|---|---|---|
| CAS Number | 874-98-6 | Molecular Weight | 201.061 | |
| Density | 1.4±0.1 g/cm3 | Boiling Point | 241.1±15.0 °C at 760 mmHg | |
| Molecular Formula | C8H9BrO | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | 95.4±21.5 °C | |
| Symbol |
GHS05 |
Signal Word | Danger | |
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Marginally designed new profen analogues have the potential to inhibit cyclooxygenase enzymes.
Arch. Pharm. (Weinheim) 348(1) , 55-61, (2015) The current structure-activity relationship of profens (i.e., 2-arylpropionic acid derivatives, a class of non-steroidal anti-inflammatory drugs) discusses the importance of α-monomethyl substitution on these compounds, since the activities obtained through t... |
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Sequential one-pot ruthenium-catalyzed azide-alkyne cycloaddition from primary alkyl halides and sodium azide.
J. Org. Chem. 76(7) , 2355-9, (2011) An experimentally simple sequential one-pot RuAAC reaction, affording 1,5-disubstituted 1H-1,2,3-triazoles in good to excellent yields starting from an alkyl halide, sodium azide, and an alkyne, is reported. The organic azide is formed in situ by treating the... |
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Mild conversion of beta-diketones and beta-ketoesters to carboxylic acids.
J. Org. Chem. 71 , 4516-4520, (2006) A mild protocol for the conversion of beta-ketoesters and beta-diketones to carboxylic acids with use of CAN in CH3CN is described. The method is compatible with a number of functional groups, and can generate carboxylic acids under neutral conditions at room... |
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Distributed Drug Discovery, Part 2: global rehearsal of alkylating agents for the synthesis of resin-bound unnatural amino acids and virtual D(3) catalog construction.
J. Comb. Chem. 11 , 14-33, (2009) Distributed Drug Discovery (D(3)) proposes solving large drug discovery problems by breaking them into smaller units for processing at multiple sites. A key component of the synthetic and computational stages of D(3) is the global rehearsal of prospective rea... |
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Highly diastereoselective alkylation of vicinal dianions of chiral succinic acid derivatives: a new general strategy to (R)-ß-arylmethyl-?-butyrolactones. Pohmakotr M, et al.
Tetrahedron Lett. 45(22) , 4315-4318, (2004)
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Synthesis of (-)-kainic acid using chiral lithium amides in an asymmetric dearomatizing cyclization. Clayden J, et al.
Tetrahedron 58(23) , 4727-4733, (2002)
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Application of sulfur ylide mediated epoxidations in the asymmetric synthesis of ß-hydroxy-d-lactones. Synthesis of a mevinic acid analogue and (+)-prelactone B. Aggarwal VK, et al.
Tetrahedron Asymmetry 60(43) , 9725-9733, (2004)
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