P24055
1-Phenyl-1,2-ethanediol
97%
Synonyme(s) :
(±)-1-Phenyl-1,2-ethanediol, (±)-Phenylethylene glycol
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A propos de cet article
Formule linéaire :
C6H5CH(OH)CH2OH
Numéro CAS:
Poids moléculaire :
138.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-258-1
Beilstein/REAXYS Number:
1306723
MDL number:
Assay:
97%
Form:
solid
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97%
form
solid
bp
272-274 °C/760 mmHg (lit.)
mp
66-68 °C (lit.)
SMILES string
OCC(O)c1ccccc1
InChI
1S/C8H10O2/c9-6-8(10)7-4-2-1-3-5-7/h1-5,8-10H,6H2
InChI key
PWMWNFMRSKOCEY-UHFFFAOYSA-N
Classe de stockage
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Ashwini C Mathpati et al.
Journal of biotechnology, 262, 1-10 (2017-09-30)
Kinetic resolution of rac-1,2-diols using the biocatalyst Burkholderia cepacia lipase (BCL) immobilized on a biodegradable binary blend support of hydroxypropyl methyl cellulose(HPMC)/polyvinyl alcohol (PVA) has been investigated. The immobilization technique improved enzyme activity significantly and it has excellent recyclability with
Lingyun Rui et al.
Applied and environmental microbiology, 71(7), 3995-4003 (2005-07-08)
DNA shuffling and saturation mutagenesis of positions F108, L190, I219, D235, and C248 were used to generate variants of the epoxide hydrolase of Agrobacterium radiobacter AD1 (EchA) with enhanced enantioselectivity and activity for styrene oxide and enhanced activity for 1,2-epoxyhexane
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