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| (-)-B-METHOXYDIISOPINOCAMPHEYLBORANE Basic information |
| Product Name: | (-)-B-METHOXYDIISOPINOCAMPHEYLBORANE | | Synonyms: | (+)-B-methoxydiisocamphenylborane;(-)-B-METHOXYDIISOPINOCAMPHEYLBORANE;(-)-B-METHOXYDIISOPINOCAMPHEYLBORANE HYDRATE;(-)-DIISOPINOCAMPHEYLMETHOXYBORANE HYDRATE;(+)-B-Methoxydiisopinocampheylborane;(+)-B-Methoxydiisopinocampheylborane,(+)-Diisopinocampheylmethoxyborane;(-)-beta-Methoxydiisopinocampheylboranehydrate;Borinic acid, B,B-bis[(1S,2R,3S,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-3-yl]-, methyl ester | | CAS: | 99438-28-5 | | MF: | C21H37BO | | MW: | 316.33 | | EINECS: | | Product Categories: | | Mol File: | 99438-28-5.mol |
| (-)-B-METHOXYDIISOPINOCAMPHEYLBORANE Chemical Properties |
| Boiling point | 365.6±9.0 °C(Predicted) | | density | 0.95±0.1 g/cm3(Predicted) | | Fp | >230 °F | | storage temp. | 2-8°C | | BRN | 6370228 |
| (-)-B-METHOXYDIISOPINOCAMPHEYLBORANE Usage And Synthesis |
| Uses | (+)?-?B-?Methoxydiisopinocamp?heylborane is a chiral catalyst used in synthetic organic chemistry such as the bacterial macrolide glycoside (-?)?-?Lyngbyaloside B which maintains antiproliferative activity. | | Uses | Reactant involved in:- Oxidative cyclization and alkylation for synthesis of ionomycin
- Intramolecular conjugate addition for tetrahydropyran synthesis
- Aldol addition and Suzuki coupling reactions
- Allylation
- Synthesis of alkanols
| | Uses | (-)-B-Methoxydiisopinocampheylborane hydrate is an intermediate used in the synthesis of homoallylic alcohol''s and several complex natural products. |
| (-)-B-METHOXYDIISOPINOCAMPHEYLBORANE Preparation Products And Raw materials |
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