29097-31-2 Usage
Uses
Used in Organic Synthesis:
Phenol, 2,2'-sulfinylbis[4-chloro(6CI,7CI,8CI,9CI) is used as a key intermediate in organic synthesis for the creation of various complex organic molecules. Its unique structure allows for versatile chemical reactions, making it a valuable component in the synthesis of specialty chemicals.
Used in Pharmaceutical Production:
In the pharmaceutical industry, Phenol, 2,2'-sulfinylbis[4-chloro(6CI,7CI,8CI,9CI) is used as a precursor for the development of new drugs. Its chemical properties enable the formation of diverse medicinal compounds, contributing to the advancement of pharmaceutical research and drug discovery.
Used in Agrochemical Production:
Phenol, 2,2'-sulfinylbis[4-chloro(6CI,7CI,8CI,9CI) also finds application in the agrochemical sector, where it serves as a starting material for the synthesis of various agrochemicals. Its role in this industry is crucial for the development of effective crop protection products and other agricultural chemicals.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, Phenol, 2,2'-sulfinylbis[4-chloro(6CI,7CI,8CI,9CI) is employed as a building block for the synthesis of novel bioactive compounds. Its unique structure and reactivity make it a promising candidate for the development of new therapeutic agents and pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 29097-31-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,0,9 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 29097-31:
(7*2)+(6*9)+(5*0)+(4*9)+(3*7)+(2*3)+(1*1)=132
132 % 10 = 2
So 29097-31-2 is a valid CAS Registry Number.
29097-31-2Relevant academic research and scientific papers
Javadi, Ali,Abouzari-Lotf, Ebrahim,Mehdipour-Ataei, Shahram,Zakeri, Masoumeh,Nasef, Mohamed Mahmoud,Ahmad, Arshad,Ripin, Adnan
, p. 2867 - 2877 (2015)
High-refractive-index polyamides (PAs) are developed by incorporation of sulfide- or sulfoxide linkages and chlorine substituents. The PAs are synthesized through the polycondensation of two novel diamine monomers, 2,2′-sulfide-bis(4-chloro-1-(4-aminophenoxy) phenyl ether (3a) and 2,2′-sulfoxide-bis(4-chloro-1-(4-aminophenoxy) phenyl ether (3b), with various aromatic diacids (a-e). The ortho-sulfide or sulfoxide units, pendant chlorine groups, and flexible ether linkages in the diamine monomers endowed the obtained PAs with excellent solubilities in organic solvents. The resulting PAs showed high thermal stability, with 10% weight loss temperatures exceeding 415°C under nitrogen and 399°C in air atmosphere. The combination of chlorine substituents, sulfide or sulfoxide linkages, and ortho-catenated structures provided polymers with high transparency along with high refractive index values of up to 1.7401 at 632.8 nm and low birefringences (0.0075). The structure-property relationships of the analogous PAs containing sulfide or sulfoxide linkages were also studied in detail by comparing the results.
