Identification | More | [Name]
(R)-2-Oxiranylanisole | [CAS]
71031-02-2 | [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 | [Molecular Formula]
C9H10O2 | [MDL Number]
MFCD06795822 | [Molecular Weight]
150.17 | [MOL File]
71031-02-2.mol |
Safety Data | Back Directory | [Hazard Codes ]
T | [Risk Statements ]
R45:May cause cancer. R20/21:Harmful by inhalation and in contact with skin . R37/38:Irritating to respiratory system and skin . R41:Risk of serious damage to eyes. R43:May cause sensitization by skin contact. R52/53:Harmful to aquatic organisms, may cause long-term adverse effects in the aquatic environment . R68:Possible risk of irreversible effects. | [Safety Statements ]
S53:Avoid exposure-obtain special instruction before use . S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) . S61:Avoid release to the environment. Refer to special instructions safety data sheet . | [RIDADR ]
NA 1993 / PGIII | [WGK Germany ]
3
| [F ]
10-23 | [HS Code ]
29109000 |
Hazard Information | Back Directory | [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 |
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Company Name: |
Energy Chemical
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