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1,2-Benzenediol, 4-ethyl-3-fluoro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

158641-49-7

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158641-49-7 Usage

Molecular Structure

Contains a benzene ring with two hydroxyl (OH) groups at the 1 and 2 positions, a fluorine atom at the 3 position, and an ethyl group at the 4 position.

Pharmaceuticals

Used in the production of various pharmaceutical compounds.

Dyes

Utilized in the synthesis of different dye compounds.

Organic Compounds

Serves as a starting material for the synthesis of other fluorinated organic compounds.

Antioxidant

Exhibits antioxidant properties, which can help prevent oxidative damage in various applications.

Organic Synthesis

Due to its unique structure and properties, it has potential applications in the field of organic synthesis.

Medicinal Chemistry

Its properties make it a candidate for further exploration in the development of new drugs and pharmaceuticals.

Safety and Handling

As with any chemical compound, appropriate safety measures should be taken when handling 1,2-Benzenediol, 4-ethyl-3-fluoro-, including the use of personal protective equipment and proper disposal methods.

Check Digit Verification of cas no

The CAS Registry Mumber 158641-49-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,6,4 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 158641-49:
(8*1)+(7*5)+(6*8)+(5*6)+(4*4)+(3*1)+(2*4)+(1*9)=157
157 % 10 = 7
So 158641-49-7 is a valid CAS Registry Number.

158641-49-7Downstream Products

158641-49-7Relevant academic research and scientific papers

Synthesis and EPR Investigations of Fluorocatecholamines

Stegmann, Hartmut B.,Deuschle, Gabriele,Schuler, Paul

, p. 547 - 556 (2007/10/02)

The synthesis of 3-fluoro and 5-fluoronoradrenaline (3- and 5-fluoronorepinephrine) starting from 4-fluorophenol or 3-fluoroanisole is described.In the first step the second OH group is introduced followed by O-methylation and subsequent introduction of a

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