42830
2,3-Diphenyl-2,3-butanediol
technical, mixture of racemic and meso forms, ≥90% (GC)
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
C6H5C(CH3)(OH)C(OH)(CH3)C6H5
CAS Number:
Molecular Weight:
242.31
EC Number:
216-665-7
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1878154
MDL number:
InChI key
URPRLFISKOCZHR-UHFFFAOYSA-N
InChI
1S/C16H18O2/c1-15(17,13-9-5-3-6-10-13)16(2,18)14-11-7-4-8-12-14/h3-12,17-18H,1-2H3
SMILES string
CC(O)(c1ccccc1)C(C)(O)c2ccccc2
grade
technical
assay
≥90% (GC)
General description
2,3-Diphenyl-2,3-butanediol is a pinacol. A mixture of meso and rac-2,3-diphenyl-2,3-butanediol is formed during the reduction of acetophenone. 2,3-Diphenyl-2,3-butanediol forms 2,3-diphenyl-1,3-butadiene by dehydration.
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Head to head polymers-38. An improved synthesis of head to head polystyrene.
Foldes E, et al.
European Polymer Journal, 29(2), 321-330 (1993)
Comparative study of the NMR length scale of dynamic heterogeneities of three different glass formers.
Reinsberg SA, et al.
Journal of Non-Crystalline Solids, 307, 208-214 (2002)
Mechanism of electrochemical pinacolization. The first asymmetric synthesis in a chiral medium.
Seebach D and Oei HA.
Angewandte Chemie (International Edition in English), 14(9), 634-636 (1975)
Dialkyl Peroxide-Induced Reductions of Aromatic Ketones.
Huyser ES and Neckers DC.
Journal of the American Chemical Society, 85(22), 3641-3644 (1963)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service