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(1S-endo)-1,7,7-trimethylbicyclo[2.2.1]hept-2-yl acrylate

  • CAS No.: 67253-41-2
  • Purity: 99%
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(1S-endo)-1,7,7-trimethylbicyclo[2.2.1]hept-2-yl acrylate Good Manufacturer supply High Quality 67253-41-2

  • Molecular Formula: C13H22O2
  • Molecular Weight: 209.30464
  • Vapor Pressure: 0.00415mmHg at 25°C 
  • Boiling Point: 247.5°C at 760 mmHg 
  • Flash Point: 80.1°C 
  • PSA: 29.46000 
  • Density: 1.01g/cm3 
  • LogP: 2.72220 

(1S-endo)-1,7,7-trimethylbicyclo[2.2.1]hept-2-yl acrylate(Cas 67253-41-2) Usage

General Description

(1S-endo)-1,7,7-trimethylbicyclo[2.2.1]hept-2-yl acrylate is a chemical compound with a unique molecular structure that consists of a bicyclic ring system with a double bond attached to a carboxylic acid group. It is classified as an acrylate, which means it contains the acrylic functional group. (1S-endo)-1,7,7-trimethylbicyclo[2.2.1]hept-2-yl acrylate is most commonly used as a monomer in the production of various polymers and plastics. Its unique structure and reactivity make it useful in the synthesis of materials with specific physical and chemical properties. Additionally, it can be used in the production of adhesives, coatings, and other industrial applications.

InChI:InChI=1/C13H22O2/c1-5-13(4,14)15-11-8-9-6-7-10(11)12(9,2)3/h5,9-11,14H,1,6-8H2,2-4H3/t9?,10-,11?,13?/m1/s1

67253-41-2 Relevant articles

Preparation method of bio-derived isobornyl (meth) acrylate

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Paragraph 0033-0036; 0041-0044; 0049-0052, (2021/01/15)

The invention belongs to the technical f...

Preparation method of isobornyl acrylate

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Paragraph 0049-0056, (2020/12/30)

The invention provides a preparation met...

Ru(II)-Catalyzed Oxidative Olefination of Benzamides: Switchable Aza-Michael and Aza-Wacker Reaction for Synthesis of Isoindolinones

Kumar, Manoj,Verma, Akhilesh K.,Verma, Shalini

supporting information, (2020/06/25)

Selective tandem oxidative C-H olefinati...

Ruthenium(II) Catalysed Highly Regioselective C-3 Alkenylation of Indolizines and Pyrrolo[1,2-a]quinolines

Jadhav, Pankaj Pandit,Kahar, Nilesh Machhindra,Dawande, Sudam Ganpat

supporting information, p. 7831 - 7835 (2019/12/24)

Discovered the Ruthenium(II) catalysed h...

67253-41-2 Process route

acrylic acid anhydride
2051-76-5

acrylic acid anhydride

(1R,2R,4S)-1,7,7-trimethylbicyclo[2.2.1]hexane-2-ol

(1R,2R,4S)-1,7,7-trimethylbicyclo[2.2.1]hexane-2-ol

isobornyl acrylate
16868-11-4,67253-41-2,69175-26-4

isobornyl acrylate

Conditions
Conditions Yield
With sulfuric acid; In toluene; at 60 - 80 ℃; for 4.5h; Solvent;
98.9%
camphene
5794-04-7

camphene

acrylic acid
79-10-7

acrylic acid

isobornyl acrylate
136374-53-3,16868-11-4,67253-41-2,69175-26-4

isobornyl acrylate

Conditions
Conditions Yield
With 10H-phenothiazine; for 0.5h; Reagent/catalyst; UV-irradiation;
92.8%

67253-41-2 Upstream products

  • 464-43-7
    464-43-7

    borneol

  • 814-68-6
    814-68-6

    acryloyl chloride

  • 5794-04-7
    5794-04-7

    camphene

  • 79-10-7
    79-10-7

    acrylic acid

67253-41-2 Downstream products

  • 74793-59-2
    74793-59-2

    3-Methylene-cyclopentanecarboxylic acid (1R,2S,4R)-1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl ester

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