+1 858-523-8231
Login | Register
menu
AA Blocks, Building Blocks, Catalysts, Inhibitors
Login | Register
152-18-1,MFCD00014888
Catalog No.:AA003V0O

152-18-1 | TRIMETHYL THIOPHOSPHATE

Pack Size
Purity
Availability
Price(USD)
Quantity
  
10g
95%
in stock  
$89.00   $63.00
- +
25g
95%
in stock  
$188.00   $132.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
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  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
0  
Isotope Atom Count:
0  
Rotatable Bond Count:
3  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
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

Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
Submit
SDS
Related Products of 152-18-1
23754-87-2

23754-87-2
Building Blocks
More >
Historical Records
88-60-8

88-60-8

 1369347-95-4

1369347-95-4

 2126179-12-0

2126179-12-0

 941931-21-1

941931-21-1
Tags:152-18-1 Molecular Formula|152-18-1 MDL|152-18-1 SMILES|152-18-1 TRIMETHYL THIOPHOSPHATE
Catalog No.: AA003V0O
152-18-1,MFCD00014888
152-18-1 | TRIMETHYL THIOPHOSPHATE
Pack Size： 10g
Purity： 95%
in stock
$89.00 $63.00
Pack Size： 25g
Purity： 95%
in stock
$188.00 $132.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
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
BP: 82 °C(Press: 20 Torr)  
Storage: 2-8℃;Inert atmosphere;  
Complexity: 85.7  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 8  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 0  
Isotope Atom Count: 0  
Rotatable Bond Count: 3  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 1.2  
Downstream Synthesis Route
15088-78-5    121-45-9    152-18-1    97754-54-6 

[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]

15088-78-5    121-45-9    71-36-3    152-18-1    122-43-0 

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

Literature fold

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 Society20101124

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

Journal: Organic & biomolecular chemistry20070207

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

Journal: Environmental monitoring and assessment20030901

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 systems19970801

Related Products of of 152-18-1
23754-87-2
23754-87-2
Building Blocks More >
18719-58-9
18719-58-9
TRIS(2-CHLOROETHYL)-ORTHOFORMATE
AA003V49 | MFCD00000971
18911-76-7
18911-76-7
Yttrium(iii) hexafluoro-2,4-pentanedionate
AA003VA4 | MFCD00064764
999-82-6
999-82-6
2-Bromoethylphosphonic acid
AA003VL9 | MFCD00013957
89598-97-0
89598-97-0
5-Bromo-2-hydroxyphenylboronic acid
AA003WRT | MFCD00093408
891270-35-2
891270-35-2
4-(1H-Pyrazol-1-yl)phenylboronic acid
AA003Y87 | MFCD06739055
895367-68-7
895367-68-7
3-Chloro-n-(2-fluorobenzyl)propanamide
AA0040HF | MFCD08076778
89050-76-0
89050-76-0
4H-Pyran-4-one, tetrahydro-3,3,5,5-tetramethyl-
AA0042AS | MFCD21648548
89006-96-2
89006-96-2
5-(Propan-2-yl)-1,3-oxazole-4-carboxylic acid
AA0044RP | MFCD07376161
885279-20-9
885279-20-9
2-(3-Fluoro-phenyl)-thiazole-4-carbaldehyde
AA0045S3 | MFCD06738361
885275-03-6
885275-03-6
5-Fluoro-2-piperidin-3-yl-1h-benzimidazole dihydrochloride
AA0046YV | MFCD06739000
Historical Records
88-60-8
88-60-8
1369347-95-4
1369347-95-4
2126179-12-0
2126179-12-0
941931-21-1
941931-21-1
Submit
© 2017 AA BLOCKS, INC. All rights reserved.