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Lithium, (triphenylsilyl)-, also known as lithium triphenylsilylide, is a chemical compound with the formula Li(SiPh3). It is a colorless, crystalline solid that is highly sensitive to air and moisture. Lithium, (triphenylsilyl)- is a strong base and a powerful nucleophile, making it a valuable reagent in organic synthesis. It is commonly used in the formation of silyl ethers and as a reducing agent in various chemical reactions. Due to its reactivity, it is typically stored under an inert atmosphere and handled with extreme care.

791-30-0

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791-30-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 791-30-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,9 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 791-30:
(5*7)+(4*9)+(3*1)+(2*3)+(1*0)=80
80 % 10 = 0
So 791-30-0 is a valid CAS Registry Number.

791-30-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name lithium,triphenylsilanide

1.2 Other means of identification

Product number -
Other names (triphenylsilyl)lithium

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:791-30-0 SDS

791-30-0Relevant academic research and scientific papers

Boron-metal exchange reaction of silylboranes with organometallic reagents: A new route to arylsilyl anions

Kawachi, Atsushi,Minamimoto, Takashi,Tamao, Kohei

, p. 1216 - 1217 (2007/10/03)

The boron-metal exchange reaction of (arylsilyl)boranes with alkyllithiums, potassium tert-butoxide, and methylmagnesium bromide affords the corresponding silyllithium, silylpotassium, and silylmagnesium compounds, respectively. Especially, the boron-lithium exchange reaction occurs even in hydrocarbon solvents such as toluene and hexane as well as in THF.

Alkylation and acylation of some activated aromatic substrates by organosilicon compounds

Artamkina, G. A.,Kovalenko, S. V.,Beletskaya, I. P.,Reutov, O. A.

, p. 139 - 150 (2007/10/02)

A method of alkylation and acylation of trinitrobenzene employing the oxidation of anionic ?-complexes generated from organosilicon reagents in the presence of KF/18-crown-6 ether is described.The method enables the introduction of alkyl and acyl substitu

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