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| | (5S)-2 2 3-TRIMETHYL-5-PHENYLMETHYL-4-I& Basic information |
| Product Name: | (5S)-2 2 3-TRIMETHYL-5-PHENYLMETHYL-4-I& | | Synonyms: | (S)-5-Benzyl-2,2,3-trimethylimidazolidin-4-one hydrochloride;(5S)-(-)-2,2,3-TriMethyl-5-benzyl-4-iMidazolidinone Monohydrochloride 97%;(S)-(-)-5-Benzyl-2,2,3-trimethyl-4-imidazolidinone Hydrochloride (This product is only available in Japan.);(5S)-2,2,3-Trimethyl-5-benzyl-4-imidazolidinone
Hydrochloride,99%e.e.;(5S)-2 2 3-TRIMETHYL-5-PHENYLMETHYL-4-I&;(5S)-(-)-2,2,3-Trimethyl-5-benzyl-4-imidazolidinone monohydrochloride;(5S)-2,2,3-TriMethyl-5-benzyl-4-iMidazolidinone hydrochloride;4-Imidazolidinone, 2,2,3-trimethyl-5-(phenylmethyl)-, hydrochloride (1:1), (5S)- | | CAS: | 278173-23-2 | | MF: | C13H18N2O.ClH | | MW: | 254.759 | | EINECS: | | | Product Categories: | | | Mol File: | 278173-23-2.mol |  |
| | (5S)-2 2 3-TRIMETHYL-5-PHENYLMETHYL-4-I& Chemical Properties |
| Melting point | 157-161 °C(lit.) | | optical activity | [α]20/D -67°, c = 1 in H2O |
| | (5S)-2 2 3-TRIMETHYL-5-PHENYLMETHYL-4-I& Usage And Synthesis |
| Uses | Metal-free OrganoCatalyst technology for asymmetric catalysis. Catalyzes asymmetric Diels-Alder reactions, 1,3-dipolar additions and pyrrole alkylations in high enantiomeric excess. |
| | (5S)-2 2 3-TRIMETHYL-5-PHENYLMETHYL-4-I& Preparation Products And Raw materials |
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