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6143-29-9

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6143-29-9 Structure

6143-29-9 Structure
IdentificationMore
[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
Chemical PropertiesBack Directory
[Appearance]

CLEAR COLORLESS TO FAINTLY YELLOW LIQUID
[Boiling point ]

73-76 °C14 mm Hg(lit.)
[density ]

1.044 g/mL at 25 °C(lit.)
[refractive index ]

n20/D 1.47(lit.)
[Fp ]

144 °F
[storage temp. ]

2-8°C
[form ]

clear liquid
[color ]

White to Yellow to Green
[InChI]

InChI=1S/C9H12O2/c1-6(10)11-9-5-7-2-3-8(9)4-7/h2-3,7-9H,4-5H2,1H3
[InChIKey]

DRWRVXAXXGJZIO-UHFFFAOYSA-N
[SMILES]

C12CC(C=C1)CC2OC(=O)C
[CAS DataBase Reference]

6143-29-9(CAS DataBase Reference)
[EPA Substance Registry System]

Bicyclo[2.2.1]hept-5-en-2-ol, acetate (6143-29-9)
Safety DataBack Directory
[Safety Statements ]

S24/25:Avoid contact with skin and eyes .
[WGK Germany ]

3
[HS Code ]

29153900
[Storage Class]

10 - Combustible liquids
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Vinyl acetate-->Dicyclopentadiene
Hazard InformationBack 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.
Spectrum DetailBack Directory
[Spectrum Detail]

5-NORBORNEN-2-YL ACETATE(6143-29-9)1HNMR
5-NORBORNEN-2-YL ACETATE(6143-29-9)IR
5-NORBORNEN-2-YL ACETATE(6143-29-9)FT-IR
5-NORBORNEN-2-YL ACETATE(6143-29-9)Raman
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

6143-29-9(sigmaaldrich)
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