ChemicalBook > CAS DataBase List > TRIISOPROPYLSILANETHIOL

TRIISOPROPYLSILANETHIOL

Product Name
TRIISOPROPYLSILANETHIOL
CAS No.
156275-96-6
Chemical Name
TRIISOPROPYLSILANETHIOL
Synonyms
Triisopropylsilylthiol;tris(propan-2-yl)silanethiol;SKL291;TRIISOPROPYLSILANETHIOL;Triisopropylsilanethiol 97%;Triisopropylsilanethiol 95%+;ri(propan-2-yl)-sulfanylsilane;tri(propan-2-yl)-sulfanylsilane;1,1,1-Tris(1-methylethyl)silanethiol;Silanethiol,1,1,1-tris(1-methylethyl)-
CBNumber
CB2783365
Molecular Formula
C9H22SSi
Formula Weight
190.42
MOL File
156275-96-6.mol
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TRIISOPROPYLSILANETHIOL Property

Boiling point:
70-75 °C2 mm Hg(lit.)
Density 
0.887 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.479(lit.)
Flash point:
171 °F
solubility 
Soluble in most organic solvents.
pka
9.86±0.10(Predicted)
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
RIDADR 
UN 3334
WGK Germany 
3
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
429937
Product name
Triisopropylsilanethiol
Purity
97%
Packaging
1g
Price
$66.8
Updated
2024/03/01
Sigma-Aldrich
Product number
429937
Product name
Triisopropylsilanethiol
Purity
97%
Packaging
5g
Price
$231
Updated
2024/03/01
American Custom Chemicals Corporation
Product number
ORS0000953
Product name
TRIISOPROPYLSILANETHIOL
Purity
95.00%
Packaging
1G
Price
$649.91
Updated
2021/12/16
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TRIISOPROPYLSILANETHIOL Chemical Properties,Usage,Production

Physical properties

bp 70–73 °C (2 mmHg); d 0.887 g cm?3.

Uses

Triisopropylsilanethiol is convenient synthetic equivalent of H2S for the synthesis of alkanethiols and unsymmetrical dialkyl sulfides; used as polarityreversal catalyst in radical reactions.
1. Use as a Nucleophile: A Synthetic Equivalent of H2S. HSTIPS is prepared in quantitative yield (98%) from the reaction of LiSH (readily obtained by reacting H2S with n-BuLi in THF) with TIPSCl at ?78°C.
2.Synthesis of 9-BBN-derived Alkyl and Aryl Boranes.
3.Palladium-catalyzed Cross-coupling Reactions. The Pd0- catalyzed cross-coupling of vinyl and aryl halides with KSTIPS affords the corresponding silyl sulfides, which can be used either to prepare thiols or sulfides.
4.Use as Ligand in Ziegler-Natta Polymerization of Ethylene in Solution. A medium pressure process for the polymerization of ethylene has been developed in the presence of a catalytic system involving a monocyclopentadienyl titanium species, containing TIPSthiolate as the heteroligand and two activable ligands (2Cl or 2Me), associated with an ionic activator such as triphenylcarbenium tetrakis(pentafluorophenyl)borate.
5.Use in Radical Reactions. The radical reduction of alkyl halides by silanes is promoted by thiols. According to Roberts, the thiol acts as a polarity-reversal catalyst.6.

TRIISOPROPYLSILANETHIOL Preparation Products And Raw materials

Raw materials

Preparation Products

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156275-96-6, TRIISOPROPYLSILANETHIOLRelated Search:


  • TRIISOPROPYLSILANETHIOL
  • 1,1,1-Tris(1-methylethyl)silanethiol
  • Triisopropylsilylthiol
  • Triisopropylsilanethiol 97%
  • Silanethiol,1,1,1-tris(1-methylethyl)-
  • Triisopropylsilanethiol 95%+
  • tri(propan-2-yl)-sulfanylsilane
  • tris(propan-2-yl)silanethiol
  • ri(propan-2-yl)-sulfanylsilane
  • SKL291
  • 156275-96-6
  • C9H22SSi
  • CH32CH3SiSH
  • Others
  • Organosilicon
  • Organometallic Reagents
  • Organometallic Reagents
  • Organosilicon
  • Others
  • Chemical Synthesis
  • Organometallic Reagents