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152-18-1,MFCD00014888
Catalog No.:AA003V0O

152-18-1 | TRIMETHYL THIOPHOSPHATE

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10g
95%
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$89.00   $63.00
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25g
95%
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$188.00   $132.00
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA003V0O
Chemical Name:
TRIMETHYL THIOPHOSPHATE
CAS Number:
152-18-1
Molecular Formula:
C3H9O3PS
Molecular Weight:
156.1405
MDL Number:
MFCD00014888
SMILES:
COP(=S)(OC)OC
Properties
Properties
 
BP:
82 °C(Press: 20 Torr)  
Storage:
2-8℃;Inert atmosphere;  

Computed Properties
 
Complexity:
85.7  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
4  
Rotatable Bond Count:
3  
XLogP3:
1.2  

Downstream Synthesis Route

[1]TetrahedronLetters,1989,vol.30,p.6757-6760

6846-35-1    121-45-9   
thiocarbamoylisothiocyanate 
  152-18-1 

[1]Hanusek,Jiří;Russell,MarkA.;Laws,AndrewP.;Page,MichaelI.[TetrahedronLetters,2007,vol.48,#3,p.417-419]

[1]Patent:WO2017/223258,2017,A1.Locationinpatent:Page/Pagecolumn36

Literature

Title: Mechanistic and computational study of a palladacycle-catalyzed decomposition of a series of neutral phosphorothioate triesters in methanol.

Journal: Journal of the American Chemical Society 20101124

Title: Mechanism of the sulfurisation of phosphines and phosphites using 3-amino-1,2,4-dithiazole-5-thione (xanthane hydride).

Journal: Organic & biomolecular chemistry 20070207

Title: Determination of organophosphorus pesticides and related compounds in water samples by membrane extraction and gas chromatography.

Journal: Environmental monitoring and assessment 20030901

Title: Selective inhibition and induction of CYP activity discriminates between the isoforms responsible for the activation of butylated hydroxytoluene and naphthalene in mouse lung.

Journal: Xenobiotica; the fate of foreign compounds in biological systems 19970801

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SDS
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