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(4-chlorophenyl)(fluoro)dimethylsilane is a chemical compound with the molecular formula C8H10ClFSi. It is a silane derivative characterized by the presence of a chlorine atom and a fluorine atom attached to a phenyl ring, along with two methyl groups connected to the silicon atom. (4-chlorophenyl)(fluoro)dimethylsilane is known for its reactivity and potential toxicity, necessitating careful handling and adherence to safety protocols.

62244-51-3

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62244-51-3 Usage

Uses

Used in Organic Synthesis:
(4-chlorophenyl)(fluoro)dimethylsilane is utilized as a reagent in organic synthesis, particularly for the preparation of organosilicon compounds. Its unique structure allows for various chemical reactions, making it a valuable component in this field.
Used in Pharmaceutical Production:
(4-chlorophenyl)(fluoro)dimethylsilane serves as a building block in the production of pharmaceuticals. Its specific functional groups enable it to be a part of the synthesis process for certain drugs, contributing to the development of new medications.
Used in Agrochemicals:
(4-chlorophenyl)(fluoro)dimethylsilane is also used in the creation of agrochemicals, which are chemicals specifically designed for use in agriculture. Its role in this industry is similar to its function in pharmaceuticals, acting as a component in the synthesis of various agrochemical products.
Used in Materials Science:
In the field of materials science, (4-chlorophenyl)(fluoro)dimethylsilane has applications in the development of polymers and coatings with enhanced properties. Its incorporation into these materials can lead to improved characteristics such as durability, resistance to environmental factors, or specific optical or electronic properties.
Used in the Coatings Industry:
(4-chlorophenyl)(fluoro)dimethylsilane is used as a component in the development of advanced coatings. These coatings can benefit from the compound's properties, potentially leading to products with improved performance, such as increased resistance to wear, better adhesion, or enhanced barrier properties.

Check Digit Verification of cas no

The CAS Registry Mumber 62244-51-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,2,4 and 4 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 62244-51:
(7*6)+(6*2)+(5*2)+(4*4)+(3*4)+(2*5)+(1*1)=103
103 % 10 = 3
So 62244-51-3 is a valid CAS Registry Number.

62244-51-3SDS

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 (4-chlorophenyl)-fluoro-dimethylsilane

1.2 Other means of identification

Product number -
Other names (4-chloro-phenyl)-fluoro-dimethyl-silane

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:62244-51-3 SDS

62244-51-3Relevant academic research and scientific papers

Preparation of the iodides (Me3Si)2C(SiMe2C6H4Y)(SiMe2I) and some related compounds

Eaborn, Colin,Jones, Karen L.,Lickiss, Paul D.

, p. 35 - 42 (2007/10/02)

The preparations of: (a) the iodides (Me3Si)2C(SiMe2C6H4Y)(SiMe2I) (Y=H, p-OMe, p-Me, p-Cl, m-CF3), via the corresponding hydrides; (b) the compounds (Me3Si)2C(SiMe2Ph)(SiMe2X) with X=F, O2CCF3, OMe, N3, NCS and Cl: and (c) the iodide (p-MeC6H4)3CSiMe2I are described. Key words: Silicon; Iodide; Fluoride; Hydride; Trimethylsilyl

Zur Synthese von Siloxanen XI. Spaltung von Siloxanen durch Bortrifluorid

Scheim, U.,Porzel, A.,Ruehlmann, K.

, p. 31 - 38 (2007/10/02)

The cleavage of siloxane bonds by BF3 was investigated kinetically by 1H NMR spectroscopy.The reactions could be evaluated by use ofa pseudo-first order rate law, when a sufficiently large excess of BF3 was used.The order with respect to BF3 was found to be 4.7.The rate constants obtained could be correlated to ?*- values with a ρ*-value of -1.0.The ?*-value found previously by 29Si NMR spectroscopy for the Me3SiO group of 0.35 was confirmed.

REACTIONS IN THE CHLOROSILANE-SILANOL-SILOXANE SYSTEM

Ruehlmann, K.

, p. 139 - 152 (2007/10/02)

We obtained the first ?*-values and ES-values for siloxy groups by spectroscopic and kinetic methods.Detailed mechanistic investigations are performed on the hydrolysis of chlorosilanes, the cleavage of Si-O-Si bonds by HCl, and the substituent exchange reaction between silanols and chlorosilanes.

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