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Bicyclo[2.2.1]hept-5-en-2-ylmethyl bicyclo[2.2.1]hept-5-ene-2-carboxylate is a bicyclic chemical compound featuring two adjacent seven-membered rings. This versatile molecule, characterized by a double bond and a carboxylic acid ester functional group, is widely utilized in organic chemistry as a building block and intermediate for synthesizing a variety of compounds. Its unique structure and reactivity are particularly valuable in the creation of complex organic molecules across different fields, including pharmaceuticals, agrochemicals, and materials science.

1218-65-1

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1218-65-1 Usage

Uses

Used in Organic Chemistry:
Bicyclo[2.2.1]hept-5-en-2-ylmethyl bicyclo[2.2.1]hept-5-ene-2-carboxylate serves as a key building block and intermediate in the synthesis of various organic compounds. Its presence in organic chemistry is attributed to its ability to participate in reactions such as hydrogenation, hydrolysis, and acylation, which are crucial for constructing complex molecular structures.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, bicyclo[2.2.1]hept-5-en-2-ylmethyl bicyclo[2.2.1]hept-5-ene-2-carboxylate is employed as a precursor for the development of novel drug molecules. Its unique bicyclic structure and functional groups make it an ideal candidate for the synthesis of bioactive compounds with potential therapeutic applications.
Used in Agrochemical Industry:
Bicyclo[2.2.1]hept-5-en-2-ylmethyl bicyclo[2.2.1]hept-5-ene-2-carboxylate also finds application in the agrochemical industry, where it is used as a starting material for the synthesis of new agrochemicals. Its reactivity and structural features contribute to the development of innovative products with improved performance in agricultural applications.
Used in Materials Science:
In the realm of materials science, bicyclo[2.2.1]hept-5-en-2-ylmethyl bicyclo[2.2.1]hept-5-ene-2-carboxylate is utilized for the synthesis of advanced materials with unique properties. Its incorporation into material formulations can lead to the development of new materials with enhanced characteristics, such as improved mechanical strength, thermal stability, or chemical resistance.

Check Digit Verification of cas no

The CAS Registry Mumber 1218-65-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,1 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1218-65:
(6*1)+(5*2)+(4*1)+(3*8)+(2*6)+(1*5)=61
61 % 10 = 1
So 1218-65-1 is a valid CAS Registry Number.
InChI:InChI=1/C16H20O2/c17-16(15-8-11-2-4-13(15)6-11)18-9-14-7-10-1-3-12(14)5-10/h1-4,10-15H,5-9H2

1218-65-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-bicyclo[2.2.1]hept-2-enylmethyl bicyclo[2.2.1]hept-2-ene-5-carboxylate

1.2 Other means of identification

Product number -
Other names EINECS 214-938-5

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:1218-65-1 SDS

1218-65-1Downstream Products

1218-65-1Relevant academic research and scientific papers

Aluminum trisphenoxide polymer as a Lewis acidic, solid catalyst

Saito, Susumu,Murase, Masaaki,Yamamoto, Hisashi

, p. 57 - 58 (2007/10/03)

A newly introduced, solid polymer of an aluminum trisphenoxide has been demonstrated an efficient catalyst for promoting the Diels-Alder reaction of α,β-enals.

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