Dipropyl chlorophosphate

Base Information

• Chemical Name: Dipropyl chlorophosphate
• CAS No.: 2510-89-6
• Molecular Formula: C6H14ClO3P
• Molecular Weight: 200.602
• Hs Code.: 2931900090
• DSSTox Substance ID: DTXSID20179787
• Nikkaji Number: J23.981J
• Wikidata: Q72469462
• Mol file: 2510-89-6.mol

Synonyms:Dipropyl chlorophosphate;2510-89-6;1-[chloro(propoxy)phosphoryl]oxypropane;Dipropyl phosphorochloridate;Phosphorochloridic acid, dipropyl ester;Propyl phosphorochloridate;Phosphorochloridicacid, dipropyl ester;Dipropyl chloridophosphate;Dipropyl phosphorochloride;Di-n-propyl chlorophosphate;O,O-dipropyl chlorophosphate;SCHEMBL177846;(Chlorodipropoxy)phosphine oxide;DTXSID20179787;MGWMBNBSQQGLAW-UHFFFAOYSA-N;BBL100451;GEO-01250;MFCD00012382;STL554245;AKOS005254616;1-[chloranyl(propoxy)phosphoryl]oxypropane;FT-0625296;A817646

Chemical Property of Dipropyl chlorophosphate

Chemical Property:

• Vapor Pressure: 0.0935mmHg at 25°C
• Refractive Index: 1.426
• Boiling Point: 231.7 °C at 760 mmHg
• Flash Point: 100.1 °C
• PSA: 45.34000
• Density: 1.14g/cm³
• LogP: 3.18650
• XLogP3: 1.7
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 6
• Exact Mass: 200.0369090
• Heavy Atom Count: 11
• Complexity: 128

Purity/Quality:

97% ^*data from raw suppliers

DipropylChlorophosphate ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCOP(=O)(OCCC)Cl

Technology Process of Dipropyl chlorophosphate

There total 2 articles about Dipropyl chlorophosphate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 30.8%

tetrachloromethane (56-23-5) + Dipropyltrimethylsilylphosphit (55755-15-2) → 1,1,3,3-tetramethyl-1,3-disiletane (1627-98-1) + chloro-trimethyl-silane (75-77-4) + chloroform (67-66-3,8013-54-5) + di-n-propyl trichloromethylphosphonate (53582-73-3) + dipropyl chlorophosphate (2510-89-6)

Guidance literature:

at 45 - 55 ℃; for 3h; Product distribution;

DOI:10.1007/BF00959203

Reference yield:

S-methyl O,O-dipropyl phosphorothioate (5301-73-5) → S-methyl-O-propyl phosphorchloridothioate (134125-84-1) + C10H24O6P2S (134125-83-0) + dipropyl chlorophosphate (2510-89-6) + O,O-dipropyl chlorothiophosphate (2524-05-2)

Guidance literature:

With sulfuryl dichloride; In toluene; at -20.1 ℃;

Reference yield: 98.0%

5-methyl-N-phenyl-4,5-dihydrothiazol-2-amine (13163-27-4) + dipropyl chlorophosphate (2510-89-6) → {5-Methyl-2-[(Z)-phenylimino]-thiazolidin-3-yl}-phosphonic acid dipropyl ester

Guidance literature:

In benzene;

upstream raw materials:

tetrachloromethane

Dipropyltrimethylsilylphosphit

S-methyl O,O-dipropyl phosphorothioate

Downstream raw materials:

phosphoric acid dipropyl ester-m-tolyl ester

di-n-propyl fluorophosphate

dipropylphosphate

2-(O,O-Dipropyl-phosphonooxy)-1-methacryloyloxy-ethan