154113
4-メトキシ-α-メチルベンジルアルコール
99%
別名:
(4-Methoxyphenyl)methylcarbinol, (±)-1-(4-Methoxyphenyl)-1-ethanol, (±)-1-(4-Methoxyphenyl)ethanol, (±)-1-(p-Methoxyphenyl)ethanol, 1-(4-Methoxyphenyl)ethan-1-ol
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この商品について
化学式:
CH3OC6H4CH(CH3)OH
CAS番号:
分子量:
152.19
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
222-019-5
MDL number:
Assay:
99%
Form:
liquid
Quality Level
assay
99%
form
liquid
refractive index
n20/D 1.533 (lit.)
bp
95 °C/1 mmHg (lit.)
density
1.079 g/mL at 25 °C (lit.)
functional group
hydroxyl
SMILES string
COc1ccc(cc1)C(C)O
InChI
1S/C9H12O2/c1-7(10)8-3-5-9(11-2)6-4-8/h3-7,10H,1-2H3
InChI key
IUUULXXWNYKJSL-UHFFFAOYSA-N
Application
4-Methoxy-α-methylbenzyl alcohol was used to study the steady-state and nanosecond, laser-flash photolysis.
保管分類
10 - Combustible liquids
wgk
WGK 3
flash_point_f
165.2 °F - closed cup
flash_point_c
74 °C - closed cup
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
第4類:引火性液体 + 第三石油類 + 危険等級III + 非水溶性液体
fsl
154113-100ML: + 154113-VAR: + 154113-BULK: + 154113-25ML:
jan
Tiziana Del Giacco et al.
Physical chemistry chemical physics : PCCP, 10(1), 200-210 (2007-12-14)
Steady-state and nanosecond laser flash photolysis measurements of 4-methoxybenzyl alcohol (1a), 4-methoxy-alpha-methylbenzyl alcohol (1b), 4,4'-dimethoxydiphenylmethanol (1c) and 4-methoxy-alpha,alpha'-dimethylbenzyl alcohol (1d) were carried out in air-equilibrated CH(2)Cl(2) and CH(3)CN solutions, in the presence of 9,10-dicyanoanthracene (DCA) and N-methylquinolinium tetrafluoroborate (NMQ(+)BF(4)(-)) as
Fanyu Zhang et al.
Nature communications, 11(1), 1431-1431 (2020-03-20)
The production of 2D metal-organic frameworks (MOFs) with highly exposed active surfaces is of great importance for catalysis. Here we demonstrate the formation of MOF nanosheets by utilizing CO2 as a capping agent to control the oriented growth of MOF. This
Xiao-Hong Chen et al.
PloS one, 9(4), e94543-e94543 (2014-04-18)
A novel carbonyl reductase (AcCR) catalyzing the asymmetric reduction of ketones to enantiopure alcohols with anti-Prelog stereoselectivity was found in Acetobacter sp. CCTCC M209061 and enriched 27.5-fold with an overall yield of 0.4% by purification. The enzyme showed a homotetrameric