2-(Acetyloxy)-3-[[2-(acetyloxy)-5-bromophenyl]methyl]-5-bromo-benzenemethanol Acetate
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Catalog numberA188065
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PricePlease ask
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Size2,5 mg
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Chemical available in other sizesPlease inquire size and price
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Stock availabilityPlease Inquire
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Cas numberThis product doesn't have CAS Number
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Chemical s molecular weight466.16
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Chemical s main applications2-(Acetyloxy)-3-[[2-(acetyloxy)-5-bromophenyl]methyl]-5-bromo-benzenemethanol Acetate is an intermediate in the synthesizing Albuterol Dimer (A514515), which is an impurity of Albuterol (Salbutamol) (A514500).
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Other name1-(2-Acetyl-3-(2-acetyl-5-bromobenzyl)-5-bromophenyl)propan-2-one;
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Chemical s formulaC20H18Br2O3
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Physical propertiesWhite Solid
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Melting temperatureNo Data Available
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Boiling temperatureNo Data Available
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Chemical s soluble inAcetic Acid, DCM, Ethyl Acetate, Methanol
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Stability conditionsNo Data Available
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StorageRoom Temperature
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DescriptionA methyl group is an alkyl derived from methane, containing one carbon atom bonded to three hydrogen atoms — CH3. In formulas, the group is often abbreviated Me. Such hydrocarbon groups occur in many organic compounds. It is a very stable group in most molecules. While the methyl group is usually part of a larger molecule, it can be found on its own in any of three forms anion, cation or radical. The anion has eight valence electrons, the radical seven and the cation six. All three forms are highly reactive and rarely observed,
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Gene target
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Short name2-(Acetyloxy)-3-[[2-(acetyloxy)-5-bromophenyl]methyl]-5-bromo-benzenemethanol Acetate
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Alternative name2-(Acetyloxy)-3-[[2-(acetyloxy)-5-bromophenyl]methyl]-5-bromo-benzenemethanol Acetate
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MeSH Data
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Name
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ConceptScope note: The insertion of recombinant DNA molecules from prokaryotic and/or eukaryotic sources into a replicating vehicle, such as a plasmid or virus vector, and the introduction of the resultant hybrid molecules into recipient cells without altering the viability of those cells.
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Tree numbers
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Qualifiersdrug effects, methods, radiation effects