| Identification | More | [Name]
5-NORBORNEN-2-YL ACETATE | [CAS]
6143-29-9 | [Synonyms]
5-NORBORNEN-2-YL ACETATE
5-NORBORNENE-2-YL ACETATE
BICYCLO[2.2.1]-5-HEPTEN-2-YL ACETATE
BICYCLO[2.2.1]HEPT-5-EN-2-YL ACETATE
TIMTEC-BB SBB008463
2-acetoxy-5-norbornene
5-Norbornen-2-yl acetate, mixture of endo and exo
Acetic acid, 5-norbornen-2-yl ester
Acetic acid, bicyclo[2.2.1]hept-5-en-2-yl ester
Bicyclo[2.2.1]hept-5-en-2-ol, acetate
norborn-5-en-2-yl acetate
5-Norbornene-2-ol acetate
5-NORBORNEN-2-YL ACETATE, 98%, MIXTURE O F ENDO AND EXO
5-(Acetoxy)bicyclo[2.2.1]hepta-2-ene
5-Acetoxybicyclo[2.2.1]hept-2-ene
5-Acetoxynorborn-2-ene
Acetic acid norborn-5-en-2-yl ester
Bicyclo[2.2.1]hepta-2-ene-5-ol acetate
Norborna-5-ene-2-ol acetate | [EINECS(EC#)]
228-144-1 | [Molecular Formula]
C9H12O2 | [MDL Number]
MFCD00167565 | [Molecular Weight]
152.19 | [MOL File]
6143-29-9.mol |
| Hazard Information | Back Directory | [Chemical Properties]
CLEAR COLORLESS TO FAINTLY YELLOW LIQUID | [Uses]
5-Norbornen-2-yl acetate (mixture of endo and exo) was used to study the ring opening metathesis polymerization of norbornene catalysed by dinuclear complex Cp*2Os2Br4 (Cp*=pentamethylcyclopentadienyl) and related compounds. | [Biochem/physiol Actions]
5-Norbornen-2-yl acetate undergoes copolymerisation with ethylene by nickel catalyst system to form high molecular weight functionalized polyethylene bearing ester functionalities. -Norbornen-2-yl acetate is the starting reagent for synthesis of urea condensation products from a-dicarbonyl compounds using Bi (OTf)3 catalyst. |
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