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97203-62-8

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97203-62-8 Usage

General Description

2-(Trimethylsilyl)ethanol is a chemical compound with the molecular formula C5H14OSi. It is a clear, colorless liquid that is insoluble in water but soluble in organic solvents. This chemical is commonly used as a reagent in organic synthesis, particularly in the preparation of silyl ethers, which are used as protecting groups in organic chemistry. 2-(Trimethylsilyl)ethanol can also serve as a building block for the synthesis of various organic compounds, including pharmaceuticals and agrochemicals. Additionally, this chemical is known for its ability to stabilize reactive intermediates and as a versatile starting material for the production of a wide range of functionalized compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 97203-62-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,2,0 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 97203-62:
(7*9)+(6*7)+(5*2)+(4*0)+(3*3)+(2*6)+(1*2)=138
138 % 10 = 8
So 97203-62-8 is a valid CAS Registry Number.
InChI:InChI=1/C5H14OSi/c1-7(2,3)5-4-6/h6H,4-5H2,1-3H3

97203-62-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-trimethylsilylethanesulfonyl chloride

1.2 Other means of identification

Product number -
Other names -

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:97203-62-8 SDS

97203-62-8Downstream Products

97203-62-8Relevant articles and documents

Synthesis of Methanethial S-Oxide (Sulfine) and Alkanethial S,S-Dioxides by Fluorodesilylation. Stereochemistry of Their Cyclopentadiene Diels-Alder Adducts

Block, Eric,Wall, Alan

, p. 1425 - 1428 (1985)

Fluorodesilylation of trimethylsilylmethanesulfinyl chloride 4 in the presence of cyclopentadiene gives 2-thiabicyclohept-5-ene endo-2-oxide, 5; in a like manner 1-trimethylsilylalkanesulfonic anhydrides afford endo- and exo-3-alkyl-2-thiabicyclohept-5-ene 2,2-dioxides, with the endo isomer predominating.Sulfine and alkyl sulfenes are invoked.

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