16807-29-7

Basic information

• Product Name: Disulfide, bis(3,4,5-trimethoxyphenyl)
• Synonyms: bis-(3,4,5-trimethoxyphenyl)disulfide;bis(3,4,5-trimethoxyphenyl)disulphide;bis(3,4,5-trimethoxyphenyl)disulfide;bis(3,4,5-trimethoxyphenyl) disulfide
• CAS NO: 16807-29-7
• Molecular Formula: C18H22O6S2
• Molecular Weight: 398.501
• Mol File: 16807-29-7.mol
• Article Data: 4

Chemical Properties

• Melting Point: 135-145 °C(Solv: ethanol (64-17-5))
• Boiling Point: 494.5±45.0 °C(Predicted)
• Density: 1.28±0.1 g/cm3(Predicted)
• CAS DataBase Reference: Disulfide, bis(3,4,5-trimethoxyphenyl)(CAS DataBase Reference)
• NIST Chemistry Reference: Disulfide, bis(3,4,5-trimethoxyphenyl)(16807-29-7)
• EPA Substance Registry System: Disulfide, bis(3,4,5-trimethoxyphenyl)(16807-29-7)

Safety Data

• Hazardous Substances Data: 16807-29-7(Hazardous Substances Data)

Upstream product

• 433935-37-6 O-ethyl-S-(3,4,5-trimethoxyphenyl)carbonodithioate 
• 24313-88-0 3,4,5-Trimethoxyaniline 
• 16807-30-0 3,4,5-trimethoxyphenylmercaptan 

Downstream Products

• 883980-08-3 3-[(3,4,5-trimethoxyphenyl)thio]-1H-indole-2-carboxylic acid 
• 1337932-61-2 5-methoxy-2-(thiophen-2-yl)-3-[(3,4,5-trimethoxyphenyl)thio]-1H-indole 
• 1337932-60-1 2-(1H-pyrrol-3-yl)-3-[(3,4,5-trimethoxyphenyl)thio]-1H-indole 
• 1337932-87-2 2-(thiophen-3-yl)-3-[(3,4,5-trimethoxyphenyl)thio]-1H-indole 
• 1337932-86-1 2-(furan-3-yl)-3-[(3,4,5-trimethoxyphenyl)thio]-1H-indole 
• 1314802-67-9 2-(thiophen-2-yl)-3-[(3',4',5'-trimethoxyphenyl)thio]-1H-indole 
• 1314802-66-8 2-(1H-pyrrol-2-yl)-3-[(3,4,5-trimethoxyphenyl)thio]-1H-indole 
• 1337932-84-9 2-(furan-2-yl)-3-[(3,4,5-trimethoxyphenyl)thio]-1H-indole 

Relevant articles and documents

Aerobic Oxidative C-H Azolation of Indoles and One-Pot Synthesis of Azolyl Thioindoles by Flavin-Iodine-Coupled Organocatalysis

The aerobic oxidative cross-coupling of indoles with azoles driven by flavin-iodine-coupled organocatalysis has been developed for the green synthesis of 2-(azol-1-yl)indoles. The coupled organocatalytic system enabled the one-pot three-component synthesis of 2-azolyl-3-thioindoles from indoles, azoles, and thiols in an atom-economical manner by utilizing molecular oxygen as the only sacrificial reagent.

ARYLTHIOINDOLE TUBULIN POLYMERIZATION INHIBITORS AND METHODS OF TREATING OR PREVENTING CANCER USING SAME

The present invention features arylthioindole compounds, pharmaceutical compositions of arylthioindole compounds and methods of treating a patient suffering from cancer or inflammatory, cardiac, or helminthic diseases, the method comprising administering