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品質等級
化驗
98%
形狀
solid
mp
66-69 °C (lit.)
官能基
bromo
SMILES 字串
COc1ccc(Br)cc1C
InChI
1S/C8H9BrO/c1-6-5-7(9)3-4-8(6)10-2/h3-5H,1-2H3
InChI 密鑰
UDLRGQOHGYWLCS-UHFFFAOYSA-N
一般說明
4-Bromo-2-methylanisole can be prepared by the bromination of o-methylanisole (2-methylanisole). It can also be prepared via reaction between 1-butyl-3-methylimidazolium tribromide [(Bmim)Br3] and an activated aromatic compound. It participates as a substrate for the a-arylation of sulphonamide in a study.
應用
4-Bromo-2-methylanisole may be used in the synthesis of 4-isopropyl-2-methylphenol and 4-methoxy-3-methylphenol.
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
個人防護裝備
Eyeshields, Gloves, type N95 (US)
(Bmim) Br3 as a New Reagent for Regioselective Monobromination of Phenols and Several Activated Aromatics under Solvent-free Conditions.
Chin. J. Chem., 23(11), 1537-1540 (2005)
The Journal of organic chemistry, 69(7), 2461-2468 (2004-03-31)
Aromatic bisabolene derivatives were prepared by two methods involving cross-coupling of organozinc reagents. The first synthesis of (+/-)-glandulone A (10), as well as syntheses of (+/-)-curcuhydroquinone (8) and (+/-)-curcuquinone (9), were accomplished via coupling of a secondary alkyl zinc reagent
Total synthesis of (?)-heliannuol D, an allelochemical from Helianthus annuus.
Tetrahedron Letters, 41(8), 1151-1154 (2000)
The isopropyl cresols.
The Journal of Organic Chemistry, 20(4), 401-411 (1955)
The Journal of organic chemistry, 62(13), 4321-4326 (1997-06-27)
It has been shown that bromodimethylsulfonium bromide, generated in situ by treating dimethyl sulfoxide with aqueous hydrobromic acid, is a milder and more selective reagent for electrophilic aromatic bromination than elemental bromine.
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