| Bioactivity | (R)-1-Phenyl-2-propanol is a chiral alcohol. (R)-1-Phenyl-2-propanol can be converted from (S)-1-phenyl-2-propanol[1][2]. |
| Name | (R)-1-Phenyl-2-propanol |
| CAS | 1572-95-8 |
| Formula | C9H12O |
| Molar Mass | 136.19 |
| Transport | Room temperature in continental US; may vary elsewhere. |
| Storage | Please store the product under the recommended conditions in the Certificate of Analysis. |
| Reference | [1]. Violetta Kiss, et al. Enantioseparation of secondary alcohols by diastereoisomeric salt formation. Chirality. 2006 Feb;18(2):116-20. [2]. Xiao-Xin Shi, et al. Asymmetric Syntheses of Both Enantiomers of Amphetamine Hydrochloride via Bakers’ Yeast Reduction of Phenylacetone. Journal of Chemical Research. 2004;2004(10):681-683. |
(R)-1-Phenyl-2-propanol
CAS: 1572-95-8 F: C9H12O W: 136.19
(R)-1-Phenyl-2-propanol is a chiral alcohol. (R)-1-Phenyl-2-propanol can be converted from (S)-1-phenyl-2-propanol.
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