212555-23-2 Usage
Description
(2,4,6-Trimethoxyphenyl)methanethiol is an organic compound characterized by its unique structure, which features a methanethiol group attached to a phenyl ring substituted with three methoxy groups at the 2nd, 4th, and 6th positions. (2,4,6-Trimethoxyphenyl)methanethiol is known for its reactivity and versatility in chemical synthesis, making it a valuable building block in various applications.
Uses
Used in Pharmaceutical Industry:
(2,4,6-Trimethoxyphenyl)methanethiol is used as a reactant for the synthesis of thiolactone polymers that mimic natural nucleosides. These synthetic nucleosides have potential applications in the development of new drugs, particularly in the treatment of viral infections and cancer, due to their ability to interfere with the replication and transcription processes of pathogens.
Used in Polymer Synthesis:
In the field of polymer chemistry, (2,4,6-Trimethoxyphenyl)methanethiol serves as a key reactant in the creation of thiolactone polymers. These polymers exhibit unique properties, such as enhanced stability and reactivity, which can be exploited in various industrial applications, including the development of advanced materials with tailored properties for use in electronics, coatings, and adhesives.
Used in Chemical Research:
(2,4,6-Trimethoxyphenyl)methanethiol is also utilized as a research compound in academic and industrial laboratories. Its unique structure and reactivity make it an interesting subject for studying various chemical reactions and mechanisms, contributing to the advancement of knowledge in organic chemistry and related fields.
Check Digit Verification of cas no
The CAS Registry Mumber 212555-23-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,2,5,5 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 212555-23:
(8*2)+(7*1)+(6*2)+(5*5)+(4*5)+(3*5)+(2*2)+(1*3)=102
102 % 10 = 2
So 212555-23-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H14O3S/c1-11-7-4-9(12-2)8(6-14)10(5-7)13-3/h4-5,14H,6H2,1-3H3
212555-23-2Relevant articles and documents
Dynamic and Responsive DNA-like Polymers
Mavila, Sudheendran,Worrell, Brady T.,Culver, Heidi R.,Goldman, Trevor M.,Wang, Chen,Lim, Chern-Hooi,Domaille, Dylan W.,Pattanayak, Sankha,McBride, Matthew K.,Musgrave, Charles B.,Bowman, Christopher N.
, p. 13594 - 13598 (2018)
The synthesis of thiolactone monomers that mimic natural nucleosides and engage in robust ring opening polymerizations (ROP) is herein described. As each repeat unit contains a thioester functional group, dynamic rearrangement of the polymer is feasible v
Aziridine-mediated ligation and site-specific modification of unprotected peptides
Dyer, Frank Brock,Park, Chung-Min,Joseph, Ryan,Garner, Philip
supporting information; experimental part, p. 20033 - 20035 (2012/01/31)
A synthesis of aziridine-containing peptides via the Cu(II)-promoted coupling of unprotected peptide thioacids and N-H aziridine-2-carbonyl peptides is reported. The unique reactivity of the resulting N-acylated aziridine-2-carbonyl peptides facilitates t
Direct synthesis of di- and trimethoxybenzyl thiols from the corresponding alcohol
Vetter, Stefan
, p. 3219 - 3223 (2007/10/03)
An efficient and reliable procedure for the one-pot synthesis of di- and trimethoxybenzyl thiols from the corresponding benzyl alcohol is described.
