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1-Propanone, 2-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-1-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

133464-91-2

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133464-91-2 Usage

Role

Reagent for protecting carbonyl groups in organic molecules

Application

Synthesis of pharmaceuticals and other complex organic compounds

Protecting group

tert-butyldimethylsilyl (TBDMS)

Function of protecting group

Blocks the reactivity of hydroxyl and carbonyl groups in organic molecules for selective and controlled reactions

Importance

An important tool in the field of organic chemistry for protecting carbonyl groups during synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 133464-91-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,4,6 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 133464-91:
(8*1)+(7*3)+(6*3)+(5*4)+(4*6)+(3*4)+(2*9)+(1*1)=122
122 % 10 = 2
So 133464-91-2 is a valid CAS Registry Number.

133464-91-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[tert-butyl(dimethyl)silyl]oxy-1-phenylpropan-1-one

1.2 Other means of identification

Product number -
Other names 1-Propanone,2-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-1-phenyl

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:133464-91-2 SDS

133464-91-2Relevant academic research and scientific papers

Oxygenation of Silyl Enol Ethers and Silyl Ketene Acetals with Molecular Oxygen and Aldehyde Catalyzed by Nickel(II) Complex. A Convenient Method for the Preparation of α-Hydroxy Carbonyl Compounds

Takai, Toshihiro,Yamada, Tohru,Rhode, Oliver,Mukaiyama, Teruaki

, p. 281 - 284 (2007/10/02)

In the presence of a catalytic amount of nickel(II) complex, silyl enol ethers and silyl ketene acetals are smoothly oxygenated by the combined use of molecular oxygen and aldehyde to afford α-siloxy carbonyl compounds via possible intermediates, siloxy epoxides.And on treatment of the α-siloxy carbonyl compounds with potassium fluoride α-hydroxy carbonyl compounds are obtained in good to high yields.

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