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51075-23-1

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51075-23-1 Usage

General Description

Trimethyl[(2-phenylprop-1-en-1-yl)oxy]silane is a chemical compound that belongs to the group of organosilicon compounds. It is composed of a silicon atom attached to three methyl groups and an oxygen-bridged phenylpropenyl group. trimethyl[(2-phenylprop-1-en-1-yl)oxy]silane is commonly used as a coupling agent in organic synthesis reactions, particularly in the formation of silicone polymers. Its unique structure provides increased reactivity and compatibility with various types of organic compounds, making it a versatile tool in chemical reactions. Additionally, trimethyl[(2-phenylprop-1-en-1-yl)oxy]silane is known to improve the adhesion and bonding properties of materials, making it a valuable additive in many industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 51075-23-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,0,7 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 51075-23:
(7*5)+(6*1)+(5*0)+(4*7)+(3*5)+(2*2)+(1*3)=91
91 % 10 = 1
So 51075-23-1 is a valid CAS Registry Number.

51075-23-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethyl-[(Z)-2-phenylprop-1-enoxy]silane

1.2 Other means of identification

Product number -
Other names 2-Phenylpropionalehyd-enol-trimethylsilylether

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:51075-23-1 SDS

51075-23-1Relevant articles and documents

Preparation of silyl enol ethers using (bistrimethylsilyl)acetamide in ionic liquids

Smietana, Michael,Mioskowski, Charles

, p. 1037 - 1039 (2007/10/03)

(matrix presented) Ionic liquids have been used for the preparation of silyl enol ethers from aldehydes and ketones with (bistrimethylsilyl)acetamide (BSA) in good yields.

UNERWARTETE REAKTIONSPRODUKTE VON N-METHYL-N-TRIMETHYLSILYLTRIFLUORACETAMID (MSTFA) MIT ALDEHYDEN

Ende, M.,Luftmann, H.

, p. 5167 - 5170 (2007/10/02)

Aldehydes react with MSTFA (N-methyl-N-trimethylsilyl-trifluoroacetamide) to give E/Z-silylenolethers and surprisingly addition products of the reagent to the carbonyl group.The mass spectra of the MSTFA/aliphatic aldehyde adducts are dominated by a key fragment of m/z 228 formed by elimination of the alkyl part.With MSTFA/aromatic aldehyde adducts this fragmentation is replaced by M-H and M-CH3N.8COCF3 (M-126 amu) ions.

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