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| B-ISOPINOCAMPHEYL-9-BORABICYCLO[3.3.1]NONANE Basic information |
| Product Name: | B-ISOPINOCAMPHEYL-9-BORABICYCLO[3.3.1]NONANE | | Synonyms: | S-alpine-borane (0.5M soln. in thf);S-Alpine-Borane? S-2,6,6-trimethyl-4-(9-borabicyclo(3.3.1)nonane-9-yl)-bicyclo(3.1.1)heptane;S-B-isopinocampheyl-9-borabicyclo(3.3.1)nonane;S-ALPINE-BORANE 97% NEAT LIQUID;(S)-(+)-1,2-Isopropylideneglycerol, 98% (99% ee/GLC);s-alpine-borane tm solution;isopinocampheylborane derivative;S-Alpine-Borane(R) solution | | CAS: | 42371-63-1 | | MF: | C18H31B | | MW: | 258.25 | | EINECS: | | Product Categories: | API intermediates | | Mol File: | 42371-63-1.mol |
| B-ISOPINOCAMPHEYL-9-BORABICYCLO[3.3.1]NONANE Chemical Properties |
| Boiling point | >55 °C(lit.) | | density | 0.897 g/mL at 25 °C | | Fp | 1 °F | | optical activity | [α]22/D +20°, c = 12 in THF |
| B-ISOPINOCAMPHEYL-9-BORABICYCLO[3.3.1]NONANE Usage And Synthesis |
| Uses | R- and S-Alpine-Boranes are used for asymmetric reduction of aldehydes and prochiral ketones. | | General Description | S-Alpine-Borane? is a chiral reducing agent, synthesized from (-)-α-pinene via hydroboration. |
| B-ISOPINOCAMPHEYL-9-BORABICYCLO[3.3.1]NONANE Preparation Products And Raw materials |
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![B-ISOPINOCAMPHEYL-9-BORABICYCLO[3.3.1]NONANE](/img/42371-63-1.jpg "B-ISOPINOCAMPHEYL-9-BORABICYCLO[3.3.1]NONANE")
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