685828
(R)-1-Phenylethanol
97%
동의어(들):
(+)-α-Methylbenzyl alcohol, (+)-α-Phenethyl alcohol, (+)-α-Phenylethanol, (+)-1-Phenylethanol, (+)-1-Phenylethyl alcohol, (+)-sec-Phenethyl alcohol
로그인조직 및 계약 가격 보기
크기 선택
제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
C6H5CH(OH)CH3
CAS 번호:
Molecular Weight:
122.16
MDL number:
UNSPSC 코드:
12352002
PubChem Substance ID:
NACRES:
NA.22
Quality Level
분석
97%
양식
liquid
광학 활성
[α]22/D +44.0°, c = 5%
refractive index
n20/D 1.528
density
0.9986 g/mL at 25 °C
작용기
hydroxyl
phenyl
SMILES string
C[C@@H](O)c1ccccc1
InChI
1S/C8H10O/c1-7(9)8-5-3-2-4-6-8/h2-7,9H,1H3/t7-/m1/s1
InChI key
WAPNOHKVXSQRPX-SSDOTTSWSA-N
일반 설명
(R)-1-Phenylethanol can be prepared from ethylbenzene via enantioselective hydroxylation of ethylbenzene catalyzed by peroxygenase enzyme.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
Flash Point (°F)
185.0 °F - closed cup
Flash Point (°C)
85 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Peroxygenase-Catalyzed Oxyfunctionalization Reactions Promoted by the Complete Oxidation of Methanol.
Ni Y, et al.
Angewandte Chemie (International Edition in English), 55(2), 798-801 (2016)
Sachiko Sugimoto et al.
Phytochemistry, 108, 189-195 (2014-12-03)
Three aromatic glycosides (1-3), two sulfur and nitrogen-containing compound glucosides (4, 5), and one flavonoid glycoside (6) were isolated from the leaves of Ixora undulata. Their structures were established by extensive 1D, 2D NMR, and HRESIMS experiments, and structure 4
Chromatograms
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