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线性分子式:
HOCH2CH(C6H5)OH
化学文摘社编号:
分子量:
138.16
UNSPSC Code:
12352002
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
2355547
Assay:
99%
Quality Level
assay
99%
optical activity
[α]20/D −69°, c = 1 in chloroform
bp
272-274 °C (lit.)
mp
64-67 °C (lit.)
functional group
hydroxyl, phenyl
SMILES string
OC[C@H](O)c1ccccc1
InChI
1S/C8H10O2/c9-6-8(10)7-4-2-1-3-5-7/h1-5,8-10H,6H2/t8-/m0/s1
InChI key
PWMWNFMRSKOCEY-QMMMGPOBSA-N
Application
合成不对称氢化反应的手性膦催化剂时所用的中间体。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
The Journal of Organic Chemistry, 44, 1729-1729 (1979)
J. Chem. Soc. Perkin Trans. II, 489-489 (1982)
Yao Nie et al.
Organic & biomolecular chemistry, 9(11), 4070-4078 (2011-04-21)
The application of biocatalysis to the synthesis of chiral molecules is one of the greenest technologies for the replacement of chemical routes due to its environmentally benign reaction conditions and unparalleled chemo-, regio- and stereoselectivities. We have been interested in
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