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"(Dichloro)(ethyl)(4-fluorophenyl)silane" is an organosilicon compound with the chemical formula C8H8Cl2FSi. It is a colorless liquid at room temperature and is soluble in common organic solvents. (dichloro)(ethyl)(4-fluorophenyl)silane is characterized by the presence of a silicon atom bonded to two chlorine atoms, an ethyl group, and a 4-fluorophenyl group. The 4-fluorophenyl group introduces a fluorine atom at the para position of the phenyl ring, which can significantly influence the compound's reactivity and physical properties. It is used in the synthesis of various organosilicon compounds and as a precursor in the production of silicone materials. Due to its reactivity, it is typically handled under controlled conditions to prevent unwanted side reactions.

7375-62-4

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7375-62-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7375-62-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,7 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7375-62:
(6*7)+(5*3)+(4*7)+(3*5)+(2*6)+(1*2)=114
114 % 10 = 4
So 7375-62-4 is a valid CAS Registry Number.

7375-62-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (dichloro)(ethyl)(4-fluorophenyl)silane

1.2 Other means of identification

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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

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More Details:7375-62-4 SDS

7375-62-4Relevant academic research and scientific papers

Solid phase cross-coupling reaction of aryl(halo)silanes with 4-iodobenzoic acid

Homsi, Fadi,Hosoi, Kazushi,Nozaki, Kyoko,Hiyama, Tamejiro

, p. 208 - 216 (2007/10/03)

Aryl(alkyl)(halo)silanes undergo facile and efficient palladium catalyzed cross-coupling reaction with iodobenzoic acid tethered to the Wang resin. Acid cleavage releases unsymmetrical biaryl carboxylic acids with high conversions, purities and yields.

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