69674-00-6

Basic information

• Product Name: diisopropoxythiophosphoryl isothiocyanate
• Synonyms: diisopropoxythiophosphoryl isothiocyanate
• CAS NO: 69674-00-6
• Molecular Weight: 239.299
• Mol File: 69674-00-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: diisopropoxythiophosphoryl isothiocyanate(CAS DataBase Reference)
• NIST Chemistry Reference: diisopropoxythiophosphoryl isothiocyanate(69674-00-6)
• EPA Substance Registry System: diisopropoxythiophosphoryl isothiocyanate(69674-00-6)

Safety Data

• Hazardous Substances Data: 69674-00-6(Hazardous Substances Data)

Upstream product

• 5285-87-0 phenyl thiocyanate 
• 107-56-2 O,O-diisopropyl hydrogen phosphorodithioate 
• 4251-16-5 propyl thiocyanate 
• 556-64-9 methyl thiocyanate 
• 105526-48-5 tris(diisopropoxyphosphinothioylthio)-s-triazine 
• 84549-14-4 S-ethyl diisopropyl N-thiophosphoryldithiocarbamate 
• 27205-99-8 sodium O,O-diisopropyl dithiophosphate 
• 15999-70-9 chlorosulfenyl isocyanide dichloride 
• 1122-85-6 phenyl cyanate 

Downstream Products

• 109446-06-2 (4-ethoxy-phenylthiocarbamoyl)-amidothiophosphoric acid O,O'-diisopropyl ester 
• 76473-87-5 C₂₁H₃₈N₂O₅P₂S₂ 
• 89207-05-6 C₆H₅CH₂NHC(S)NHP(OCH(CH₃)2)2S 
• 1217089-19-4 p-(4-imidazol-1-yl)-C₆H₄NHC(S)NHP(S)(OiPr)2 
• 1217089-21-8 p-NC-C₆H₄NHC(S)NHP(S)(OiPr)2 
• 1353868-99-1 6-MeO(O)CC₆H₄NHC(S)NHP(S)(O(i)Pr)2 
• 1334285-76-5 C₁₅H₂₆N₃O₂PS₂ 
• 1361326-46-6 C₁₅H₂₅N₂O₂PS₂ 
• 245411-52-3 1,2-bis-N,N'-(diisopropoxythiophosphorylthiocarbamido)phenylenediamine 
• 163627-56-3 Phenyliminomethylene-thiophosphoramidic acid O,O'-diisopropyl ester 
• 69674-01-7 N-[bis(isopropoxy)-thiophosphoryl]-N'-phenylthiourea 
• 959904-63-3 [Cu(triphenylphosphine)2(piperidin-N-yl-C(S)NP(S)(O-i-Pr)2)] 

Relevant articles and documents

REACTION OF O,O-DIALKYL DITHIOPHOSPHATES WITH CHLOROSULFENYL ISOCYANIDE DICHLORIDE

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REACTIONS OF DIALKYL DITHIOPHOSPHORIC AND DIPHENYLDITHIOPHOSPHORIC ACIDS WITH THIOCYANATES

The interaction between phosphorus(IV) dithio acid partial esters and thiocyanates proceeds with initial formation of addition products to the CN bond.These adducts are either split by the second molecule of dithio acid to S-alkyl dithiocarbamates and tetraalkyl trithiophosphates or rearrange into dialkyl N-thiophosphoryldithiocarbamates.The latter easily split off the thiols and convert to isothiocyanatothiophosphates.A number of thiophosphorylated and diphosphorylated thioureas were synthesized by the reaction of isothiocyanatothiophosphates with amines and α-aminoalkylphosphonates.