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13246-39-4

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13246-39-4 Usage

General Description

1-(Trimethylsilyl)ethanol, 98% is a chemical compound with the molecular formula C5H14OSi. It is a colorless liquid with a boiling point of 82-84°C and a density of 0.79 g/mL. This chemical is commonly used as a reagent in organic synthesis, particularly in the formation of silyl enol ethers from ketones and aldehydes. It serves as a protecting group for carbonyl compounds, as well as a precursor for various functionalized organosilanes. 1-(Trimethylsilyl)ethanol, 98% is also used in the preparation of pharmaceuticals, agrochemicals, and other fine chemicals. It should be handled and stored with proper safety precautions in a well-ventilated area away from sources of ignition.

Check Digit Verification of cas no

The CAS Registry Mumber 13246-39-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,4 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13246-39:
(7*1)+(6*3)+(5*2)+(4*4)+(3*6)+(2*3)+(1*9)=84
84 % 10 = 4
So 13246-39-4 is a valid CAS Registry Number.

13246-39-4SDS

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 1-trimethylsilylethanol

1.2 Other means of identification

Product number -
Other names trimethylsilyl-ethanol

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:13246-39-4 SDS

13246-39-4Relevant articles and documents

Synthesis of silylated alkylboronic acids and esters via hydroboration of allylic and vinylic trimethylsilanes

Cytarska,Kaczanowska,Zaidlewicz

, p. 1587 - 1594 (2008/09/18)

Representative allylic trimethylsilanes and isopropenyltrimethylsilane were hydroborated with dichloroborane, and the products were transformed into the corresponding ssor γ-trimethylsilylboronates. Synthesis of 2-trimethylsilylethylboronic acid and its diethyl ester via hydroboration of trimethylvinylsilane with diisopinocampheylborane, followed by liberation of α-pinene is described.

REGIO- AND STEREO-SELECTIVITY OF CATALYTIC HYDROALUMINATION OF OLEFINS WITH (2,6-DI-tert-BUTYL-4-METHYLPHENOXY)DIISOBUTYLALUMINIUM

Kuchin, A. V.,Nurushev, R. A.,Umanskaya, L. I.,Tolstikov, G. A.

, p. 1194 - 1199 (2007/10/02)

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