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(1S-endo)-1,7,7-trimethylbicyclo[2.2.1]hept-2-yl acrylate
- CAS No.: 67253-41-2
- Purity: 99%
(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
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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
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2051-76-5
acrylic acid anhydride
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(1R,2R,4S)-1,7,7-trimethylbicyclo[2.2.1]hexane-2-ol
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16868-11-4,67253-41-2,69175-26-4
isobornyl acrylate
| Conditions | Yield |
|---|---|
|
With
sulfuric acid;
In
toluene;
at 60 - 80 ℃;
for 4.5h;
Solvent;
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98.9%
|
-
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5794-04-7
camphene
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79-10-7
acrylic acid
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136374-53-3,16868-11-4,67253-41-2,69175-26-4
isobornyl acrylate
| Conditions | Yield |
|---|---|
|
With
10H-phenothiazine;
for 0.5h;
Reagent/catalyst;
UV-irradiation;
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92.8%
|
67253-41-2 Upstream products
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464-43-7
borneol
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814-68-6
acryloyl chloride
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5794-04-7
camphene
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79-10-7
acrylic acid
67253-41-2 Downstream products
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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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