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297156-50-4

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297156-50-4 Usage

General Description

2-Methyl-2-propenoic acid 2-(1-methylethyl)tricyclo[3.3.1.13,7]dec-2-yl ester is a chemical compound with a long, complex name that can be simplified to tricyclo[3.3.1.13,7]dec-2-yl ester. It is a synthetic compound with a unique molecular structure and is commonly used as a building block in organic synthesis. 2-Methyl-2-propenoic acid 2-(1-methylethyl)tricyclo[3.3.1.13,7]dec-2-yl ester is a colorless, viscous liquid at room temperature and is insoluble in water. It is primarily used in the manufacturing of pharmaceuticals, agrochemicals, and other specialty chemicals due to its versatile reactivity and ability to form complex structures. Additionally, it is known for its potential as a flavor and fragrance ingredient due to its unique chemical properties.

Check Digit Verification of cas no

The CAS Registry Mumber 297156-50-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,7,1,5 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 297156-50:
(8*2)+(7*9)+(6*7)+(5*1)+(4*5)+(3*6)+(2*5)+(1*0)=174
174 % 10 = 4
So 297156-50-4 is a valid CAS Registry Number.

297156-50-4 Well-known Company Product Price

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  • TCI America

  • (I0962)  2-Isopropyl-2-methacryloyloxyadamantane  >98.0%(GC)

  • 297156-50-4

  • 5g

  • 590.00CNY

  • Detail
  • TCI America

  • (I0962)  2-Isopropyl-2-methacryloyloxyadamantane  >98.0%(GC)

  • 297156-50-4

  • 25g

  • 2,150.00CNY

  • Detail

297156-50-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-propan-2-yl-2-adamantyl) 2-methylprop-2-enoate

1.2 Other means of identification

Product number -
Other names 2-Isopropyl-2-adamantyl Methacrylate

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:297156-50-4 SDS

297156-50-4Downstream Products

297156-50-4Relevant articles and documents

Preparation method and device of 2-isopropyl-2-adamantanol (methyl) acrylate

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Paragraph 0033-0034, (2019/06/07)

The invention discloses a preparation method of 2-isopropyl-2-adamantanol (methyl) acrylate, and the method is characterized in that the 2-isopropyl-2-adamantanol (methyl) acrylate is prepared from (methyl) acrylate and isopropyl adamantane alcohol as reaction raw materials by taking an alkaline compound as a catalyst and carrying out ester exchange reaction at 40-120 DEG C in the presence of a solvent, wherein the alkaline compound catalyst is loaded on a porous carrier; the reaction liquid is filtered by a plate-type filter at 60-80 DEG C and then is cooled to a temperature of -60 DEG C to 0DEG C, and a separated solid is the 2-isopropyl-2-adamantanol (methyl) acrylate. According to the invention, the alkaline compound is used for loading a porous catalyst, the production process stepsare simple, the reaction is thorough, the yield is up to more than 95%, the purification process is simple, the purity of the product reaches more than 98%, the solvent and the catalyst can be recycled, the production cost is saved, and the preparation method realizes zero emission of pollutants, and is a green production method.

METHOD FOR PRODUCING ADAMANTYL (METH)ACRYLATE COMPOUND

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Paragraph 0043, (2019/04/18)

PROBLEM TO BE SOLVED: To provide a method for producing an adamantyl (meth)acrylate compound having an extremely high purity at a high recovery rate. SOLUTION: The method for producing an adamantyl (meth)acrylate compound comprises subjecting a crude adamantyl (meth)acrylate compound produced by reacting a compound represented by the general formula (a) as given below and (meth)acrylic acid or the like to a first crystallization using at least one kind of water-soluble organic solvent and then adding water in an amount of 100 to 1 pt.mass based on 100 pts.mass of the water-soluble organic solvent to subject the same to a second crystallization. (In the formula, R1 represents H or a 1-10C alkyl group; M represents H, an alkali metal or MgX (X is halogen).) SELECTED DRAWING: None COPYRIGHT: (C)2019,JPOandINPIT

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