|
| B-ISOPINOCAMPHEYL-9-BORABICYCLO[3.3.1]NONANE Basic information |
Product Name: | B-ISOPINOCAMPHEYL-9-BORABICYCLO[3.3.1]NONANE | Synonyms: | R-ALPINE-BORANE(R);B-ISOPINOCAMPHEYL-9-BORABICYCLO[3.3.1]NONANE;(R)-B-isopinocampheyl-9-borabicyclo[3.3.1]nonane;R-2,7,7-trimethylnorpinanborabicyclo(3.3.1)nonane;R-alpine-borane (0.5M soln. in thf);R-Alpine-Borane? (R)-2,6,6-trimethyl-4-(9-borabicyclo[3.3.1]nonan-9-yl)bicyclo[3.1.1]heptane;R-ALPINE-BORANE;R-ALPINE-BORANE 97% | CAS: | 73624-47-2 | MF: | C18H31B | MW: | 258.25 | EINECS: | | Product Categories: | API intermediates | Mol File: | 73624-47-2.mol | |
| B-ISOPINOCAMPHEYL-9-BORABICYCLO[3.3.1]NONANE Chemical Properties |
Boiling point | >55 °C(lit.) | alpha | -3 º (NEAT) | density | 0.896 g/mL at 25 °C | Fp | 1 °F | optical activity | [α]21/D -22°, c = 12 in THF |
| B-ISOPINOCAMPHEYL-9-BORABICYCLO[3.3.1]NONANE Usage And Synthesis |
Uses | R-Alpine-Borane? solution may be used to prepare:
- (R)-5-(Benzyloxy)pent-3-y-2-ol, an intermediate for the stereoselective total synthesis of (-)-stagonolide D.
- (R)-1-(p-Tolyl)-1-pentyn-3-ol, an intermediate for the enatioselective synthesis of (R)-incrustoporin.
- N-(tert-Butyloxycarbonyl)-(4S)-[4-2H]-1-L-homoserine tert-butyl ester, an intermediate for synthesizing (4S)-[4-2H]-L-homoserine.
| General Description | R-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 |
|