52340-78-0
52340-78-0
Chemical Structure
(R,R)-(+)-Hydrobenzoin
- CAS No.: 52340-78-0
- Formula:C14H14O2
- Molecular Weight:214.26
IUPAC Name: (1R,2R)-1,2-diphenylethane-1,2-diol
InChIKey: IHPDTPWNFBQHEB-ZIAGYGMSSA-N
SMILES: O[C@H](C1=CC=CC=C1)[C@@H](C2=CC=CC=C2)O
Biological Activity: (R,R)-(+)-Hydrobenzoin is a chiral secondary alcohol that can be used as a key substrate or a chiral auxiliary reagent in various catalytic reactions and synthetic experiments[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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(R,R)-(+)-Hydrobenzoin | 99.82% | (R,R)-(+)-Hydrobenzoin is a chiral secondary alcohol that can be used as a key substrate or a chiral auxiliary reagent in various catalytic reactions and synthetic experiments. | ||||||||||||||||||||
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(R,R)-(+)-Hydrobenzoin (Standard) | ≥98% | (R,R)-(+)-Hydrobenzoin (Standard) is the analytical standard of (R,R)-(+)-Hydrobenzoin. This product is intended for research and analytical applications. (R,R)-(+)-Hydrobenzoin is a chiral secondary alcohol that can be used as a key substrate or a chiral auxiliary reagent in various catalytic reactions and synthetic experiments. | ||||||||||||||||||||
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References
- [1]. Kwan SooKim, et al. Synthesis of enantiopure cyclopentitols and aminocyclopentitols mediated by oxyselenenylation of cyclopentene with (R,R)-hydrobenzoin. Tetrahedron Letters. 1988.
- [2]. Shabbir SH, et al. Molecular recognition and self-assembly special feature: A general protocol for creating high-throughput screening assays for reaction yield and enantiomeric excess applied to hydrobenzoin. Proc Natl Acad Sci U S A. 2009 Jun 30;106(26):10487-92. [Content Brief]
- [3]. Tran R, Kilyanek SM. Deoxydehydration of polyols catalyzed by a molybdenum dioxo-complex supported by a dianionic ONO pincer ligand. Dalton Trans. 2019 Nov 21;48(43):16304-16311. [Content Brief]
