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6143-29-9

  • Product Name5-Norbornen-2-yl acetate
  • Molecular FormulaC9H12O2
  • Molecular Weight152.19
  • Purity99%
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Product Details

Quick Details

  • CasNo： 6143-29-9
  • Molecular Formula： C9H12O2
  • Purity： 99%

High Purity 5-Norbornene-2-yl 6143-29-9 with Competitive Price

  • Molecular Formula:C9H12O2
  • Molecular Weight:152.193
  • Appearance/Colour:clear colorless to faintly yellow liquid 
  • Vapor Pressure:5.8E-12mmHg at 25°C 
  • Melting Point:73-76 °C14 mm Hg(lit.) 
  • Refractive Index:n20/D 1.47(lit.)  
  • Boiling Point:184.7 °C at 760 mmHg 
  • Flash Point:62.2 °C 
  • PSA：26.30000 
  • Density:1.09 g/cm3 
  • LogP:1.51410 

5-NORBORNEN-2-YL ACETATE(Cas 6143-29-9) Usage

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.

InChI:InChI=1/C23H23NO4/c25-22(23-12-15-9-16(13-23)11-17(10-15)14-23)8-6-18-5-7-21(28-18)19-3-1-2-4-20(19)24(26)27/h1-8,15-17H,9-14H2/b8-6+

6143-29-9 Relevant articles

(Meth) acrylate derivative, polymer and photoresist composition having lactone structure, and method for forming pattern by using it

-

, (2008/06/13)

There are here disclosed a photoresist m...

Gas-phase Diels-Alder cycloaddition reaction in the presence of methanol and water vapor

Gholami,Talebi

, p. 79 - 83 (2007/10/03)

Hydrogen bonding effects of protic solve...

Ring-opening metathesis - Cross-metathesis reactions (ROM-CM) of substituted norbornadienes and norbornenes

Mayo, Peter,Tam, William

, p. 9513 - 9525 (2007/10/03)

Ring-opening metathesis - cross-metathes...

Effect of supramolecular inclusion on the selectivity of 3-nortricyclanylidene

Rosenberg,Brinker

, p. 1517 - 1522 (2007/10/03)

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6143-29-9 Process route

nortricyclane
279-19-6

nortricyclane

acetic acid
64-19-7,77671-22-8

acetic acid

3-Acetoxynortricyclen
6555-48-2,127127-98-4,127127-99-5

3-Acetoxynortricyclen

4-ethynylcyclopentene
330654-57-4

4-ethynylcyclopentene

5-acetoxynorborn-2-ene
2890-95-1,5257-37-4,62667-88-3,83679-37-2,99295-40-6,99295-41-7,112836-09-6,6143-29-9

5-acetoxynorborn-2-ene

Conditions
Conditions Yield
Photolysis;
84.2 % Chromat.
14.2 % Chromat.
1.6 % Chromat.
vinyl acetate
108-05-4,9003-20-7

vinyl acetate

cyclopenta-1,3-diene
542-92-7,25568-84-7,7313-32-8

cyclopenta-1,3-diene

5-acetoxynorborn-2-ene
2890-95-1,5257-37-4,62667-88-3,83679-37-2,99295-40-6,99295-41-7,112836-09-6,6143-29-9

5-acetoxynorborn-2-ene

Conditions
Conditions Yield
With water; at 22.95 ℃; Further Variations:; Reagents; Kinetics; gas-phase reaction;
 
at 22.95 ℃; gas phase reaction;
 

6143-29-9 Upstream products

  • 279-19-6
    279-19-6

    nortricyclane

  • 64-19-7
    64-19-7

    acetic acid

  • 108-05-4
    108-05-4

    vinyl acetate

  • 542-92-7
    542-92-7

    cyclopenta-1,3-diene

6143-29-9 Downstream products

  • 29583-33-3
    29583-33-3

    (+/-)-endo-norborneol acetate

  • 694-97-3
    694-97-3

    (1S,2S,4S)-bicyclo[2.2.1]hept-5-en-2-ol

  • 106928-44-3
    106928-44-3

    (1R,2R,4R)-endo-bicyclo[2.2.1]hept-5-en-2-ol

  • 154278-40-7
    154278-40-7

    (1S,2S,4S)-bicyclo[2.2.1]hept-5-en-2-yl acetate

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