93-56-1
93-56-1
Chemical Structure
1-Phenylethane-1,2-diol
Synonym(s): Styrene Glycol
- CAS No.: 93-56-1
- Formula:C8H10O2
- Molecular Weight:138.17
IUPAC Name: 1-phenylethane-1,2-diol
InChIKey: PWMWNFMRSKOCEY-UHFFFAOYSA-N
SMILES: OC(C1=CC=CC=C1)CO
Biological Activity: 1-Phenylethane-1,2-diol (Styrene Glycol) is a benzyl diol compound, which is the major metabolite of Styrene. 1-Phenylethane-1,2-diol can be oxidized to hydroxyl ketone (2-hydroxy-1-phenylethan-1-one) selectively with variety of catalysts, including organocatalysts, metal complexes, non-noble metal oxides, bimetallics[1][2][3].
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1-Phenylethane-1,2-diol | 99.24% | 1-Phenylethane-1,2-diol (Styrene Glycol) is a benzyl diol compound, which is the major metabolite of Styrene. 1-Phenylethane-1,2-diol can be oxidized to hydroxyl ketone (2-hydroxy-1-phenylethan-1-one) selectively with variety of catalysts, including organocatalysts, metal complexes, non-noble metal oxides, bimetallics. | ||||||||||||||||||||
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1-Phenylethane-1,2-diol (Standard) | ≥98% | 1-Phenylethane-1,2-diol (Standard) is the analytical standard of 1-Phenylethane-1,2-diol. This product is intended for research and analytical applications. 1-Phenylethane-1,2-diol (Styrene Glycol) is a benzyl diol compound, which is the major metabolite of Styrene. 1-Phenylethane-1,2-diol can be oxidized to hydroxyl ketone (2-hydroxy-1-phenylethan-1-one) selectively with variety of catalysts, including organocatalysts, metal complexes, non-noble metal oxides, bimetallics. | ||||||||||||||||||||
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Structural Analogs
-
Similarity Score 0.87
HY-41414(S)-(+)-2-Phenylglycinol -
Similarity Score 0.87
HY-W002038(R)-(-)-2-Phenylglycinol -
Similarity Score 0.87
HY-W0048302-Phenyl-1,3-propanediol -
Similarity Score 0.87
HY-W012618R1-Phenyl-1-propanol (Standard) -
Similarity Score 0.83
HY-W856876Tropaldehyde -
Similarity Score 0.83
HY-W041194Tropic acid -
Similarity Score 0.82
HY-N3859Erythro-1-phenylpropane-1,2-diol -
Similarity Score 0.82
HY-W087444A(S)-1-(4-Hydroxyphenyl)ethane-1,2-diol -
Explore the MedChemAI to find more analogs
References
- [1]. Fangwei Zhang, et al. Oxidation of 1-Phenylethane-1,2-Diol to 2-Hydroxy-1-Phenylethan-1-One Catalyzed by Gold Nanocrystals. ChemistrySelect. Volume 3, Issue 48 p. 13638-13640
- [2]. Bandyopadhyaya A K, et al. Synthesis of both enantiomers of 1-phenylethane-1, 2-diol via chirality transfer from bile acid derivatives[J]. Tetrahedron: Asymmetry, 2000, 11(17): 3463-3466.
- [3]. Kohn J, et al. Assessment of the neurotoxicity of styrene, styrene oxide, and styrene glycol in primary cultures of motor and sensory neurons. Toxicol Lett. 1995 Jan;75(1-3):29-37. [Content Brief]
