35190-71-7 Usage
Description
(2-([2-(Hydroxymethyl)phenyl]disulfanyl)phenyl)methanol is a chemical compound with the molecular formula C14H14O2S2. It is a white solid that is used in organic synthesis. (2-([2-(HYDROXYMETHYL)PHENYL]DISULFANYL)PHENYL)METHANOL is composed of a central methanol group attached to two phenyl rings, each of which contains a disulfanyl group and a hydroxymethyl group. It is commonly used in the formation of disulfide bonds in proteins and peptides, making it an important building block in the study of biological and pharmaceutical molecules. Additionally, it has been studied for its potential applications in materials science and catalysis.
Uses
Used in Organic Synthesis:
(2-([2-(Hydroxymethyl)phenyl]disulfanyl)phenyl)methanol is used as a building block in organic synthesis for the formation of disulfide bonds in proteins and peptides. Its unique structure allows for the creation of complex molecules that are important in the study of biological and pharmaceutical compounds.
Used in Biological and Pharmaceutical Research:
In the field of biological and pharmaceutical research, (2-([2-(Hydroxymethyl)phenyl]disulfanyl)phenyl)methanol is used as a key component in the development of new drugs and therapies. Its ability to form disulfide bonds makes it a valuable tool in the study of protein structure and function, as well as in the design of novel therapeutic agents.
Used in Materials Science:
(2-([2-(Hydroxymethyl)phenyl]disulfanyl)phenyl)methanol has been studied for its potential applications in materials science. Its unique structure and properties make it a promising candidate for the development of new materials with specific characteristics, such as improved stability or reactivity.
Used in Catalysis:
In the field of catalysis, (2-([2-(Hydroxymethyl)phenyl]disulfanyl)phenyl)methanol has been investigated for its potential use as a catalyst or catalyst precursor. Its ability to form disulfide bonds and its reactivity make it a candidate for facilitating various chemical reactions, potentially leading to more efficient and environmentally friendly processes.
Check Digit Verification of cas no
The CAS Registry Mumber 35190-71-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,1,9 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 35190-71:
(7*3)+(6*5)+(5*1)+(4*9)+(3*0)+(2*7)+(1*1)=107
107 % 10 = 7
So 35190-71-7 is a valid CAS Registry Number.
35190-71-7Relevant articles and documents
Sequential C-H activation enabled expedient delivery of polyfunctional arenes
Cai, Xiaoqing,Chen, Qian,Chen, Xiaojian,Gao, Yang,Huo, Yanping,Li, Xianwei,Ouyang, Wensen,Rao, Jianhang,Wang, Jie
supporting information, p. 8075 - 8078 (2021/08/20)
Modular construction of polyfunctional arenes from abundant feedstocks stands as an unremitting pursue in synthetic chemistry, accelerating the discovery of drugs and materials. Herein, using the multiple C-H activation strategy with versatile imidate esters, the expedient delivery of molecular libraries of densely functionalized sulfur-containing arenes was achieved, which enabled the concise construction of biologically active molecules, such as Bipenamol.
Development of a tandem base-catalyzed, triphenylphosphine-mediated disulfide reduction-Michael addition
Bartolozzi, Alessandra,Foudoulakis, Hope M.,Cole, Bridget M.
experimental part, p. 2023 - 2032 (2009/04/03)
A tandem disulfide reduction-Michael addition was developed using both free and polymer-bound triphenylphosphine as the reducing agent. The procedure was applied to intermolecular systems for the synthesis of arylsulfanyl- and alkylsulfanyl-substi-tuted p
A convenient reduction of highly functionalized aromatic carboxylic acids to alcohols with borane-THF and boron trifluoride-etherate
Chen,Iakovleva,Kesten,Magano,Rodriguez,Sexton,Zhang,Lee
, p. 665 - 670 (2007/10/03)
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