40156-12-5 Usage
Uses
Used in Organic Synthesis:
7-NORBORNADIENYLBENZENE is utilized as a precursor in organic synthesis for its ability to participate in a variety of chemical reactions, facilitating the creation of complex organic molecules.
Used in Polymer and Resin Production:
In the polymer industry, 7-NORBORNADIENYLBENZENE is employed as a crosslinking agent, which enhances the structural integrity and performance characteristics of the resulting polymers and resins.
Used in Pharmaceutical Synthesis:
7-NORBORNADIENYLBENZENE serves as a building block in the synthesis of pharmaceutical compounds, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Synthesis:
Similarly, in the agrochemical sector, 7-NORBORNADIENYLBENZENE is used as a key component in the synthesis of various agrochemicals, including pesticides and herbicides, to improve agricultural productivity and crop protection.
Proper handling and storage are imperative for 7-NORBORNADIENYLBENZENE due to its reactive properties, ensuring the safety of workers and the environment in all applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 40156-12-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,1,5 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 40156-12:
(7*4)+(6*0)+(5*1)+(4*5)+(3*6)+(2*1)+(1*2)=75
75 % 10 = 5
So 40156-12-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H12/c1-2-4-10(5-3-1)13-11-6-7-12(13)9-8-11/h1-9,11-13H
40156-12-5Relevant academic research and scientific papers
Synthesis and Use of 7-Substituted Norbornadienes for the Preparation of Prostaglandins and Prostanoids
Baxter, Anthony D.,Binns, Falmai,Javed, Tariq,Roberts, Stanley M.,Sadler, Peter,et al.
, p. 889 - 900 (2007/10/02)
Syntheses of 7-substituted norbornadienes from 7-t-butoxy- and 7-halogeno-norbornadienes are described.Rearrangement of the products in the presence of peracetic acid gives bicyclic aldehydes (2) in equilibrium with enol ethers (3) which are hydrolysed to hydroxycyclopentenylacetaldehydes (4), and converted into key intermediates for the synthesis of prostaglandins and their analogues.Syntheses of prostaglandin J analogues with n-hexyl and phenyl groups replacing the ο-side-chain are described.
