ChemicalBook--->CAS DataBase List--->1795-31-9

1795-31-9

1795-31-9 Structure

1795-31-9 Structure
IdentificationMore
[Name]

TRIS(TRIMETHYLSILYL)PHOSPHITE
[CAS]

1795-31-9
[Synonyms]

PHOSPHOROUS ACID TRIS(TRIMETHYLSILYL) ESTER
TRIS(TRIMETHYLSILYL)PHOSPHITE
Phosphorous acid, tristrimethylsilyl
Tris(trimethylsily)phosphite
Phosphorousacidtrimethylsilylester
TRIS(TRIMETHYLSILYL) PHOSPHITE 95%
TRIS(TRIMETHYLSILYL)PHOSPHITE 97+%
Phosphorous acid tri(trimethylsilyl) ester
Tris(trimethylsiloxy)phosphine
[Molecular Formula]

C9H27O3PSi3
[MDL Number]

MFCD00015588
[Molecular Weight]

298.54
[MOL File]

1795-31-9.mol
Chemical PropertiesBack Directory
[Boiling point ]

78-81 °C/8 mmHg (lit.)
[density ]

0.893 g/mL at 25 °C(lit.)
[refractive index ]

n20/D 1.409(lit.)
[Fp ]

>230 °F
[storage temp. ]

RT, stored under nitrogen
[form ]

Liquid
[color ]

Clear colorless
[Specific Gravity]

0.893
[Water Solubility ]

Sparingly soluble in water.
[Hydrolytic Sensitivity]

8: reacts rapidly with moisture, water, protic solvents
[Sensitive ]

Air & Moisture Sensitive
[BRN ]

2043814
[InChI]

InChI=1S/C9H27O3PSi3/c1-14(2,3)10-13(11-15(4,5)6)12-16(7,8)9/h1-9H3
[InChIKey]

VMZOBROUFBEGAR-UHFFFAOYSA-N
[SMILES]

[Si](C)(C)(OP(O[Si](C)(C)C)O[Si](C)(C)C)C
[CAS DataBase Reference]

1795-31-9(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P305+P351+P338-P332+P313-P337+P313
[Hazard Codes ]

Xi
[Risk Statements ]

R36/38:Irritating to eyes and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
[RIDADR ]

1760
[WGK Germany ]

3
[F ]

10-21
[TSCA ]

No
[REACH Registrations]

Active
[HazardClass ]

8
[PackingGroup ]

III
[HS Code ]

29319000
Hazard InformationBack Directory
[Uses]

Tris(trimethylsilyl) Phosphite is used in the studies of bisphosphonic acids as effective inhibitor of glutamine synthetase, a promising approach for the discovery of novel drugs against tuberculosis. It also acts as a reagent in the preparation of substituted calix[4]arenes bearing one or two α-hydroxymethylphosphonic acid fragments at upper rim of macrocycle as inhibitors of glutathione S-transferase in vitro.
[Preparation]

By silylation of anhydrous phosphorous acid (dried by repeated azeotropic evaporation of a solution in  THF with dry benzene) with excess Chlorotrimethylsilane and excess Triethylamine in dimethoxyethane, toluene, or Et2O-THF, followed by evaporation of the solvent and vacuum distillation of the residue. The residue, which contains a mixture of  tris(trimethylsilyl) phosphite and bis(trimethylsilyl) phosphonate [HP(O)(OTMS)2], can also be heated with sodium (140 °C,  13-22 h), followed by vacuum distillation to obtain pure tris(trimethylsilyl) phosphite.
[storage]

Extremely hygroscopic; use in a fume hood.
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

Tris(trimethylsilyl) phosphite, 96%(1795-31-9)
[Sigma Aldrich]

1795-31-9(sigmaaldrich)
[TCI AMERICA]

Tris(trimethylsilyl) Phosphite,>97.0%(T)(1795-31-9)
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