- (R)-2-Oxiranylanisole
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- $3.00 / 1KG
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2020-01-13
- CAS:71031-02-2
- Min. Order: 1KG
- Purity: 98%
- Supply Ability: 200KG
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| | (R)-2-Oxiranylanisole Basic information |
| Product Name: | (R)-2-Oxiranylanisole | | Synonyms: | (2R)-1,2-EPOXY-3-PHENOXYPROPANE;OXIRANE, (PHENOXYMETHYL)-, (2R)-;(R)-2-OXIRANYLANISOLE;(R)-ALPHA-(2-OXIRANYL)ANISOLE;(R)-GLYCIDYL PHENYL ETHER;RPGE;(R)-PHENYL GLYCIDYL ETHER;(R)-α-(2-Oxiranyl)anisole, (R)-Glycidyl phenyl ether | | CAS: | 71031-02-2 | | MF: | C9H10O2 | | MW: | 150.17 | | EINECS: | | | Product Categories: | API intermediates | | Mol File: | 71031-02-2.mol |  |
| | (R)-2-Oxiranylanisole Chemical Properties |
| Boiling point | 85-86 °C(Press: 0.8 Torr) | | density | 1.122±0.06 g/cm3(Predicted) | | refractive index | 1.5290 to 1.5330 | | Fp | 71 °C | | form | clear liquid | | color | Colorless to Almost colorless | | CAS DataBase Reference | 71031-02-2(CAS DataBase Reference) |
| | (R)-2-Oxiranylanisole Usage And Synthesis |
| Uses | Reactant involved in the synthesis of:
- Neuroprotective small molecules
- Piperidinol analogs for studies of anti-tuberculosis activity
- 2-Substituted 3,4-dihydro-2H-1,4-benzoxazines via cyclization of hydroxyl sulfonamides
- Bicyclic azetidines via ring opening, esterification, chlorination and intramolecular alkylation
- Bromoalkanes via ring opening and addition across C-O bonds
Involved in biological studies as a substrate for Bacillus-produced enantioselective eposide hydrolase |
| | (R)-2-Oxiranylanisole Preparation Products And Raw materials |
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