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1-Fluoro-4-(triethoxymethyl)benzene is an organic compound with the molecular formula C13H19FO3. It is a colorless liquid that is soluble in organic solvents. This chemical is characterized by the presence of a fluorine atom at the 1-position and a triethoxymethyl group (CH3CH2O)3CH- at the 4-position of a benzene ring. The triethoxymethyl group is a protecting group for the benzylic position, which can be used in various chemical reactions to prevent unwanted side reactions at that site. 1-fluoro-4-(triethoxymethyl)benzene is primarily used as an intermediate in the synthesis of pharmaceuticals and other organic compounds, taking advantage of its reactivity and the ability to selectively protect certain functional groups during chemical transformations.

10345-73-0

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10345-73-0 Usage

Fluoroalkyl compound

A compound containing a fluoroalkyl group, which is an alkyl group with fluorine atoms attached.

Benzene ring

A six-carbon ring structure with alternating single and double bonds, which is a fundamental structure in organic chemistry.

Fluoro and triethoxymethyl substituents

Two different functional groups attached to the benzene ring, a fluorine atom (-F) and a triethoxymethyl group (-CH2OC2H5)3.

Building block in organic synthesis

A compound used as a starting material or intermediate in the synthesis of more complex organic molecules.

Pharmaceutical industry application

The compound is commonly used in the production of various pharmaceuticals due to its unique properties and reactivity.

Potential intermediate in production

1-fluoro-4-(triethoxymethyl)benzene has been identified as a possible intermediate in the synthesis of agrochemicals and other related products.

Unique molecular structure and properties

The compound's specific arrangement of atoms and functional groups give it special characteristics that are valuable in the development of new materials and chemical processes.

Low toxicity

1-fluoro-4-(triethoxymethyl)benzene is considered to have a low level of toxicity, making it a relatively safe compound to handle.

Safety and handling precautions

Despite its low toxicity, it is essential to follow standard laboratory practices and safety measures when working with 1-fluoro-4-(triethoxymethyl)benzene to ensure proper handling and minimize risks.

Check Digit Verification of cas no

The CAS Registry Mumber 10345-73-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,4 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 10345-73:
(7*1)+(6*0)+(5*3)+(4*4)+(3*5)+(2*7)+(1*3)=70
70 % 10 = 0
So 10345-73-0 is a valid CAS Registry Number.

10345-73-0SDS

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 1-fluoro-4-(triethoxymethyl)benzene

1.2 Other means of identification

Product number -
Other names 1-fluoro-4-trimethoxymethyl-benzene

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:10345-73-0 SDS

10345-73-0Relevant academic research and scientific papers

Synthesis method of crude carboxylic ester (by machine translation)

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Paragraph 0021; 0022, (2020/08/09)

The method is characterized in that the carboxylic ester and the ether are prepared by reacting a carboxylic ester with an ether at a certain temperature under the catalysis of a catalyst at a certain pressure for a certain time. (by machine translation)

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