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2-NORBORNYL METHACRYLATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

29753-02-4

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29753-02-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29753-02-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,7,5 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 29753-02:
(7*2)+(6*9)+(5*7)+(4*5)+(3*3)+(2*0)+(1*2)=134
134 % 10 = 4
So 29753-02-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H16O2/c1-7(2)11(12)13-10-6-8-3-4-9(10)5-8/h8-10H,1,3-6H2,2H3

29753-02-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-bicyclo[2.2.1]heptanyl 2-methylprop-2-enoate

1.2 Other means of identification

Product number -
Other names Methacrylic acidnorbornan-2-yl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:29753-02-4 SDS

29753-02-4Downstream Products

29753-02-4Relevant academic research and scientific papers

Preparation method of (methyl)acrylate with bridged ring structure

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, (2020/06/16)

The invention relates to a preparation method of (methyl)acrylate with a bridged ring structure. The (methyl)acrylate is synthesized through three-step reaction comprising the following steps: firstly, carrying out direct addition on saturated fatty acid and bridged ring olefin or a derivative thereof; rectifying and purifying, thus removing a byproduct generated by self-polymerization of the bridged ring olefin; then carrying out hydrolysis to obtain corresponding bridged ring alcohol or a derivative thereof; finally, carrying out ester exchange reaction between the (methyl)acrylate and the bridged ring alcohol or the derivative thereof to obtain the (methyl)acrylate with the bridged ring structure. The preparation method provided by the invention is simple, and the steps are easy to operate; a target product is obtained through the three-step reaction and the yield is high; the disadvantages of a rectification process of a direct esterification technology that the requirements are high and the yield is low are overcome; the content of a residual cycloolefin monomer in the product is low; when the preparation method is applied to resin synthesis, the disadvantages that resin becomes yellow and the viscosity is increased can be remarkably relieved.

METHOD FOR PRODUCING DEUTERATED NORBORNEOL AND/OR DEUTERATED DINORBORNYL ETHER, AND METHOD FOR PRODUCING UNSATURATED CARBOXYLIC ESTER OF DEUTERATED NORBORNYL

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Page/Page column 11, (2008/06/13)

PROBLEM TO BE SOLVED: To provide a method for producing a deuterated norborneol and a deuterated dinorbornyl ether; and to provide a method for producing an unsaturated carboxylic ester of a deuterated norbornyl synthesized by using the deuterated norborneol and/or the deuterated dinorbornyl ether or the like produced by the method as a raw material. SOLUTION: The method for producing a compound represented by general formulas (I) (wherein, a part or the whole of the hydrogen atoms in a norbornene skeleton is a deuterium atom; and two or more kinds of compounds represented by general formula (I) and mutually having different structures can be included therein) and/or (II) (wherein, a part or the whole of the hydrogen atoms in a norbornene skeleton is a deuterium atom; and two or more kinds of compounds represented by general formula (II) and mutually having different structures can be included therein) involves deuterating 2-norbornene in deuterium oxide in the presence of an acid having pKa ≤1.

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