212555-23-2

Basic information

• Product Name: (2,4,6-trimethoxyphenyl)methanethiol
• Synonyms: (2,4,6-trimethoxyphenyl)methanethiol;2,4,6-Trimethoxybenzylmercaptan
• CAS NO: 212555-23-2
• Molecular Formula: C₁₀H₁₄O₃S
• Molecular Weight: 214.284
• Mol File: 212555-23-2.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 326℃
• Flash Point: 151℃
• Appearance: /
• Density: 1.117
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.528
• Storage Temp.: Inert atmosphere,Room Temperature
• PKA: 9.07±0.10(Predicted)
• CAS DataBase Reference: (2,4,6-trimethoxyphenyl)methanethiol(CAS DataBase Reference)
• NIST Chemistry Reference: (2,4,6-trimethoxyphenyl)methanethiol(212555-23-2)
• EPA Substance Registry System: (2,4,6-trimethoxyphenyl)methanethiol(212555-23-2)

Safety Data

• Hazardous Substances Data: 212555-23-2(Hazardous Substances Data)

Usage

Uses

(2,?4,?6-?Trimethoxyphenyl)?methanethiol is a reactant used in the synthesis of thiolactone polymers that mimic natural nucleosides.

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

Upstream product

• 61040-78-6 2,4,6-trimethoxybenzyl alcohol 
• 830-79-5 2,4,6-trimethoxybenzaldehyde 
• 1197342-89-4 Boc-L-Ala-STmob 

Downstream Products

• 881913-37-7 3-tert-butoxy-2-(9H-fluoren-9-ylmethoxycarbonylamino)-thiobutyric acid 2,4,6-trimethoxy-benzyl ester 
• 651305-76-9 2-cyano-thioacetimidic acid 2,4,6-trimethoxy-benzyl ester 
• 366808-14-2 (Z)-2-hydroxystyryl-2,4,6-trimethoxybenzylsulfide 
• 366808-12-0 (Z)-2-hydroxystyryl-2,4,6-trimethoxybenzylsulfone 
• 1158245-54-5 Boc-L-Phe-STmob 
• 1158245-51-2 Fmoc-L-Ala-STmob 
• 1154041-20-9 S,S'-bis(2,4,6-trimethoxybenzyl) N-benzyloxycarbonyl-L-dithioaspartate 
• 1234549-10-0 S,S'-bis(2,4,6-trimethoxybenzyl) N-tert-butoxycarbonyl-L-dithioaspartate 
• 1197342-90-7 NH₂-L-Ala-STmob 
• 1292784-04-3 S-2,4,6-trimethoxybenzyl 3,5-bis((4,8,24-trioxo-6,13,16,19-tetraoxa-3,9,23-triazaoctacos-27-yn-1-yl)oxy)benzothioate 
• 1449578-40-8 3',5'-O-(di-tert-butylsilanediyl)-2'-O-(2,4,6-trimethoxybenzylthiomethyl)uridine 

Relevant articles and documents

Dynamic and Responsive DNA-like Polymers

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

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

An efficient and reliable procedure for the one-pot synthesis of di- and trimethoxybenzyl thiols from the corresponding benzyl alcohol is described.