104608-47-1

Basic information

• Product Name: ethyl (4-benzothiazol-2-ylbenzyl)phosphonochloridate hydrochloride
• Synonyms: ethyl (4-benzothiazol-2-ylbenzyl)phosphonochloridate hydrochloride
• CAS NO: 104608-47-1
• Molecular Weight: 388.254
• Mol File: 104608-47-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: ethyl (4-benzothiazol-2-ylbenzyl)phosphonochloridate hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl (4-benzothiazol-2-ylbenzyl)phosphonochloridate hydrochloride(104608-47-1)
• EPA Substance Registry System: ethyl (4-benzothiazol-2-ylbenzyl)phosphonochloridate hydrochloride(104608-47-1)

Safety Data

• Hazardous Substances Data: 104608-47-1(Hazardous Substances Data)

Upstream product

• 24239-18-7 2-<4-(bromomethyl)phenyl>benzothiazole 
• 75889-62-2 fostedil 
• 104608-45-9 Ethyl Hydrogen 4-(Benzothiazol-2-yl)benzylphosphonate 

Downstream Products

• 127881-39-4 (4-Benzothiazol-2-yl-benzyl)-morpholin-4-yl-phosphinic acid ethyl ester 
• 127881-45-2 (4-Benzothiazol-2-yl-benzyl)-(2-oxo-thiazolidin-3-yl)-phosphinic acid ethyl ester 
• 127881-47-4 (4-Benzothiazol-2-yl-benzyl)-(3-methyl-2-oxo-imidazolidin-1-yl)-phosphinic acid ethyl ester 
• 127881-31-6 ethyl (4-benzothiazol-2-ylbenzyl)-N-isopropylamidophosphonate 
• 127881-35-0 C₂₀H₂₅N₂O₂PS 
• 128766-90-5 Ethyl 3-Hydroxypropyl 4-(Benzothiazol-2-yl)benzylphosphonate 
• 128766-87-0 (4-Benzothiazol-2-yl-benzyl)-phosphonic acid 3-bromo-propyl ester ethyl ester 
• 128766-93-8 Ethyl 3-Nitroxypropyl 4-(Benzothiazol-2-yl)benzylphosphonate 
• 128766-95-0 Ethyl 3-Acetoxypropyl 4-(Benzothiazol-2-yl)benzylphosphonate 
• 127881-49-6 ethyl (4-benzothiazol-2-ylbenzyl)(2-thioxopyrrolidino)phosphinate 
• 127881-48-5 (4-Benzothiazol-2-yl-benzyl)-(4-ethyl-2,3-dioxo-piperazin-1-yl)-phosphinic acid ethyl ester 
• 128766-86-9 (4-Benzothiazol-2-yl-benzyl)-phosphonic acid 2-bromo-ethyl ester ethyl ester 
• 128766-82-5 (4-Benzothiazol-2-yl-benzyl)-phosphonic acid sec-butyl ester ethyl ester 
• 127881-33-8 C₁₈H₂₀ClN₂O₂PS 

Relevant articles and documents

Organic phosphorus compounds. IV. Asymmetric 4-(benzothiazol-2-yl)benzylphosphonates as potent calcium antagonistic vasodilators.

Various asymmetric or cyclic ester derivatives of the phosphonic acid moiety in the calcium antagonist fostedil (KB-944) were synthesized. The coronary vasodilator activity of these compounds was assessed by Langendorff's method. Among them, the ethyl isopropyl ester 12 showed the most potent activity, which was comparable to that of fostedil.