74607-59-3

Basic information

• Product Name: 3-Butyl-2-(4-methoxy-phenyl)-4-propyl-[1,3,2]thiazaphosphetidine 2-sulfide
• CAS NO: 74607-59-3
• Molecular Weight: 329.467
• Mol File: 74607-59-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3-Butyl-2-(4-methoxy-phenyl)-4-propyl-[1,3,2]thiazaphosphetidine 2-sulfide(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Butyl-2-(4-methoxy-phenyl)-4-propyl-[1,3,2]thiazaphosphetidine 2-sulfide(74607-59-3)
• EPA Substance Registry System: 3-Butyl-2-(4-methoxy-phenyl)-4-propyl-[1,3,2]thiazaphosphetidine 2-sulfide(74607-59-3)

Safety Data

• Hazardous Substances Data: 74607-59-3(Hazardous Substances Data)

Upstream product

• 19172-47-5 Lawessons reagent 
• 924-16-3 N-nitrosodibutylamine 

Relevant articles and documents

STUDIES ON ORGANOPHOSPHORUS COMPOUNDS XXXII Reactions of 2,4-bis(4-methoxyphenyl)-1,3,2,4-dithiadiphosphetane-2,4-disulfide with compounds containing the N=O function

Reactions of 2,4-bis(4-methoxyphenyl)-1,3,2,4-dithiadiphosphetane-2,4-disulfide, 1, with a series of substrates having a semipolar bond have been studied.C-Nitroso compounds react to give azoxy compounds or azo compounds, whereas N,N-dimethyl-p-nitrosoaniline furnishes p-dimethylamino-N-thiosulfinyl-aniline, 6, and benzofurazan-1-oxide produces 2,1,3-benzothiadiazole.N-nitroso compounds react with 1 to give phosphorous heterocycles in which the N-nitroso function is destroyed.Elimination of HNO from certain N-nitroso compounds has also been observed.Nitrones and N-oxides react with 1 to form the corresponding deoxygenated products.In the case of quinoline-N-oxide, small amounts of quinoline-2-thione could be isolated in addition to the deoxygenated product.Mechanistic considerations are presented.