6618-67-3 Usage
Uses
Used in Organic Synthesis:
2,3-bis(bromomethyl)benzene-1,4-diyl diacetate is used as a cross-linking agent in the production of polymers and resins. Its reactive bromomethyl and acetate groups facilitate the formation of covalent bonds with other molecules, contributing to the structural integrity and properties of the resulting materials.
Used in Pharmaceutical and Agrochemical Industries:
2,3-bis(bromomethyl)benzene-1,4-diyl diacetate serves as a building block in the creation of various pharmaceuticals and agrochemicals. Its unique structure allows for the development of new compounds with specific therapeutic or pesticidal properties, enhancing the range of available treatments and products in these industries.
Check Digit Verification of cas no
The CAS Registry Mumber 6618-67-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,1 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6618-67:
(6*6)+(5*6)+(4*1)+(3*8)+(2*6)+(1*7)=113
113 % 10 = 3
So 6618-67-3 is a valid CAS Registry Number.
6618-67-3Relevant academic research and scientific papers
Efficient synthesis of 5,8-disubstituted-1,4-dihydrobenzoxathiin-3-oxides and their isomeric structures, 4,7-disubstituted-1,3-dihydrobenzo[b] thiophene-2,2-dioxides
Attardo, Giorgio,Wang, Wuyi,Kraus, Jean-Louis,Belleau, Bernard
, p. 4743 - 4746 (2007/10/02)
Functionalized dihydrobenzoxathiin oxides and dihydrobenzothiophene-2,2-dioxides 11-18 have been prepared via trapping of sulfur dioxide under photolytic or ground state conditions.
Capture du paradimethoxyorthoquinodimethane:syntheses de quinones et d'un intermediaire de la daunomycinone
Laduranty, Joelle,Lepage, Lucette,Lepage, Yves
, p. 1161 - 1167 (2007/10/02)
New para-dimethoxyl and para-diacetoxy derivatives in the naphthalene, anthracene, naphthacene, naphtho(2,3-c)thiophene and benzo-c-thiophene series are synthesized via the trapping of o-quinodimethanes by various dienophiles.Among these compounds, and in
