34492-32-5

Basic information

• Product Name: N,N-Bis(2-chloroethyl)aminodichlorophosphine sulfide
• Synonyms: N,N-Bis(2-chloroethyl)aminodichlorophosphine sulfide
• CAS NO: 34492-32-5
• Molecular Formula: C₄H₈Cl₄NPS
• Molecular Weight: 274.9638
• Mol File: 34492-32-5.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 314.1°Cat760mmHg
• Flash Point: 143.8°C
• Appearance: /
• Density: 1.532g/cm³
• Vapor Pressure: 0.000475mmHg at 25°C
• Refractive Index: 1.558
• CAS DataBase Reference: N,N-Bis(2-chloroethyl)aminodichlorophosphine sulfide(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-Bis(2-chloroethyl)aminodichlorophosphine sulfide(34492-32-5)
• EPA Substance Registry System: N,N-Bis(2-chloroethyl)aminodichlorophosphine sulfide(34492-32-5)

Safety Data

• Hazardous Substances Data: 34492-32-5(Hazardous Substances Data)

Usage

InChI:InChI=1/C4H8Cl4NPS/c5-1-3-9(4-2-6)10(7,8)11/h1-4H2

Upstream product

• 334-22-5 N,N-bis(chloro-2-ethyl)amine 
• 821-48-7 bis-(2-chloroethyl)amine hydrochloride 

Downstream Products

• 34492-38-1 C₁₆H₃₂Cl₂N₃PS 
• 34492-35-8 C₃₄H₄₀Cl₂N₃O₂PS 
• 34492-36-9 C₃₆H₄₄Cl₂N₃O₂PS 
• 91725-65-4 2--1,3,2-oxathiaphosphorinan-sulfid-(2) 

Relevant articles and documents

Preparation, structure, and reactivity of a new heterocyclic system-1-thio-2,8-diphenyl-2,5,8-triaza-1 λ5-phosphabicyclo[3.3.0]octane

A new heterocyclic system, 1-thio-2,8-diphenyl-2,5,8-triaza-1 λ5-phosphabicyclo[3.3.0]octane, has been prepared, and its structure was confirmed by single-crystal X-ray diffraction. Preliminary reactivity studies demonstrated a complex mechanis

In search of new organophosphorus pesticides and insecticides. Part III: Synthesis and anticholinesterase studies of 3-(subs)-quinoxy/pyridinoxy/cyclica mino-2,3-dihydro-2-(4-chlorophenyl)-1H-naphth [1,2-E][1,3,2] oxazaphosphorine 3-sulfides

In situ treatment of (cyclic) amino derivatives with the product obtained from the cyclocondensation of 1-p-chloroanilinomethyl naphthol-2 and thiophosphoryl chloride in dry benzene-THF afforded the titled oxazaphosphorine sulfides in good yield. Subsequently, the reaction of pyridinoxy/quinoxythiophosphorodi chloridates and 1-p-chloro anilino methyl naphthol-2 in dry benzene-THF mixture gave the corresponding pyridinoxy/quinoxy oxaza phosphorine 3-sulfides in quantitative yield. All the condensations proceeded smoothly by employing triethylamine to scavenge the liberated hydrogen chloride gas. Anticholinestease studies of these compounds indicated very high degree of inhibition several times higher than the reference standard-methyl parathion.