61575-01-7 Usage
Description
1,8-Diphenoxyoctane, with the molecular formula C18H22O2, is an organic compound belonging to the class of phenyl ether derivatives. It is characterized by its versatile nature and is of significant interest to chemists and researchers in the field of organic synthesis and structure-activity relationships.
Uses
Used in Organic Chemistry Research and Industry:
1,8-Diphenoxyoctane is used as a building block for the synthesis of various organic compounds, contributing to the development of new molecules with potential applications in different sectors.
Used in Pharmaceutical Production:
1,8-Diphenoxyoctane is used as a key component in the production of pharmaceuticals, where its unique structure and properties can be leveraged to create novel drugs with specific therapeutic effects.
Used in Agrochemicals:
In the agrochemical industry, 1,8-Diphenoxyoctane is utilized for the synthesis of various agrochemicals, such as pesticides and herbicides, that are essential for maintaining agricultural productivity and crop protection.
Used in Fine Chemicals Production:
1 8-DIPHENOXYOCTANE is also employed in the production of fine chemicals, which are high-purity chemicals used in various applications, including the fragrance, flavor, and specialty chemical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 61575-01-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,5,7 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 61575-01:
(7*6)+(6*1)+(5*5)+(4*7)+(3*5)+(2*0)+(1*1)=117
117 % 10 = 7
So 61575-01-7 is a valid CAS Registry Number.
61575-01-7Relevant articles and documents
Cobalt-Catalyzed Csp3?Csp3Homocoupling
Cai, Yingxiao,Qian, Xin,Gosmini, Corinne
supporting information, p. 2427 - 2430 (2016/08/16)
An efficient and easy method for Csp3?Csp3homocoupling was developed using cobalt bromide as catalyst. A series of functionalized alkyl bromides and alkyl chlorides were coupled in high yields under mild conditions. This reaction seems to involve a radical intermediate. (Figure presented.).
