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ChemicalBook--->CAS DataBase List--->71031-02-2

71031-02-2

71031-02-2 Structure

71031-02-2 Structure
IdentificationMore
[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
Chemical PropertiesBack Directory
[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)
Safety DataBack 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 InformationBack 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
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

71031-02-2(sigmaaldrich)
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