154180
4-甲氧基苯乙醇
99%
别名:
2-(4-甲氧基苯基)乙醇
登录 查看组织和合同定价。
选择尺寸
变更视图
关于此项目
线性分子式:
CH3OC6H4CH2CH2OH
化学文摘社编号:
分子量:
152.19
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
211-866-6
Beilstein/REAXYS Number:
2043563
MDL number:
Assay:
99%
Form:
solid
Quality Level
assay
99%
form
solid
bp
334-336 °C (lit.)
mp
26-28 °C (lit.)
functional group
hydroxyl
SMILES string
COc1ccc(CCO)cc1
InChI
1S/C9H12O2/c1-11-9-4-2-8(3-5-9)6-7-10/h2-5,10H,6-7H2,1H3
InChI key
AUWDOZOUJWEPBA-UHFFFAOYSA-N
General description
(R)-1-（4-甲氧基苯基）乙醇{(R)-MOPE，4-甲氧基苯乙醇，1-（4-甲氧基苯基）乙醇}，是在4-甲氧基苯乙酮（MOAP）利用固定的三角酵母AS2的生物催化抗Prelog对映选择性还原过程中形成的。
Application
4-甲氧基苯乙醇已被用于通过将其与47％的氢碘酸回流而制备4-（2-碘乙基）苯酚。它可被用于制备(2R*,4R*)-1-正-丁基-2-甲基-4-（2-氧吡咯烷-1-基）-6-甲氧基-1,2,3,4-四氢喹啉和(2R*,4S*)-1-正-丁基-2-甲基-4-（2-氧吡咯烷-1-基）-6-甲氧基-1,2,3,4-四氢喹啉。
4-甲氧基苯乙醇已在氟双相催化反应中用作内标。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Gloves, type N95 (US)
An asymmetric catalytic carbon? carbon bond formation in a fluorous biphasic system based on perfluoroalkyl-BINOL.
Tian Y and Chan KS.
Tetrahedron Letters, 41(45), 8813-8816 (2000)
Reactions of Azides with Electrophiles: New Methods for the Generation of Cationic 2-Azabutadienes. Synthesis of 1, 2, 3, 4-Tetrahydroquinolines and 1, 2-Dihydroquinolines via a Hetero Diels-Alder Reaction.
Pearson WH and Fang WK
Israel J. Chem., 37(1), 39-46 (1997)
Biocatalytic anti-Prelog stereoselective reduction of 4'-methoxyacetophenone to (R)-1-(4-methoxyphenyl) ethanol with immobilized Trigonopsis variabilis AS2. 1611 cells using an ionic liquid-containing medium.
Lou W-Y, et al.
Green Chemistry, 11(9), 1377-1384 (2009)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 154180-10G | 04061838346186 |