3119-94-6

Basic information

• Product Name: 3-ethylbenzothiazolium iodide
• Synonyms: 3-ethylbenzothiazolium iodide;3-ethylbenzo[d]thiazol-3-iuM iodide
• CAS NO: 3119-94-6
• Molecular Formula: C₉H₁₀NS*I
• Molecular Weight: 291.15187
• EINECS: 221-495-1
• Mol File: 3119-94-6.mol
• Article Data: 3

Chemical Properties

• Melting Point: 138-139 °C
• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: g/cm³
• CAS DataBase Reference: 3-ethylbenzothiazolium iodide(CAS DataBase Reference)
• NIST Chemistry Reference: 3-ethylbenzothiazolium iodide(3119-94-6)
• EPA Substance Registry System: 3-ethylbenzothiazolium iodide(3119-94-6)

Safety Data

• Hazardous Substances Data: 3119-94-6(Hazardous Substances Data)

Usage

InChI:InChI=1/C9H10NS.HI/c1-2-10-7-11-9-6-4-3-5-8(9)10;/h3-7H,2H2,1H3;1H/q+1;/p-1

Upstream product

• 16407-47-9 bis(N-ethylbenzothiazol-2-ylidene) 
• 95-16-9 1,3-Benzothiazole 
• 75-03-6 ethyl iodide 

Downstream Products

• 1197983-84-8 (E)-3-{(E)-3-[(Z)-2-(3-ethyllbenzo[d]thiazol-2(3H)-ylidene)ethylidene]-2-(pyrimidin-2-ylthio)cyclopent-1-enyl}-1-(naphthalen-2-yl)prop-2-en-1-one 
• 948996-86-9 C₃₉H₃₆N₂O₂S₂ 
• 68549-49-5 3-ethyl-2-phenylbenzothiazoline 

Relevant articles and documents

Diazadithiafulvalenes as electron donor reagents

Diazadithiafulvalenes act as excellent electron donors to arenediazonium salts. The diazadithiafulvalenium radical cations trap primary carbon radicals successfully. However, the diazadithiafulvalenium salts which form, undergo rapid ring fragmentation in contrast to their tetrathia counterparts. The Royal Society of Chemistry 1999.

Selective Formation of Triose from Formaldehyde Catalyzed by Thiazolium Salt

In the self-condensation of formaldehyde catalyzed by thiazolium salts, dihydroxyacetone (triose), but not glycolaldehyde, was formed selectively and in high yield.This is of much interest as a facile and novel synthesis of triose from this C1 compound.A mechanism which can account for the selective formation of dihydroxyacetone is described.