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2,3,5,6-tetrafluoro-4-methoxybenzaldehyde is a chemical compound with the molecular formula C8H3F4O2. It is a derivative of benzaldehyde, substituted with four fluorine atoms and a methoxy group. 2,3,5,6-tetrafluoro-4-methoxybenzaldehyde is characterized by its strong odor and is recognized for its potential in various applications due to its unique structure.

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  • 19161-44-5 Structure
  • Basic information

    1. Product Name: 2,3,5,6-tetrafluoro-4-methoxybenzaldehyde
    2. Synonyms: 2,3,5,6-tetrafluoro-4-methoxybenzaldehyde
    3. CAS NO:19161-44-5
    4. Molecular Formula:
    5. Molecular Weight: 208.112
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 19161-44-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2,3,5,6-tetrafluoro-4-methoxybenzaldehyde(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,3,5,6-tetrafluoro-4-methoxybenzaldehyde(19161-44-5)
    11. EPA Substance Registry System: 2,3,5,6-tetrafluoro-4-methoxybenzaldehyde(19161-44-5)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 19161-44-5(Hazardous Substances Data)

19161-44-5 Usage

Uses

Used in Organic Synthesis:
2,3,5,6-tetrafluoro-4-methoxybenzaldehyde is used as a building block in organic synthesis for its ability to contribute to the formation of complex organic molecules. Its fluorinated and methoxylated structure allows for versatile reactions, making it a valuable intermediate in the synthesis of a wide range of compounds.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 2,3,5,6-tetrafluoro-4-methoxybenzaldehyde is used as a key intermediate for the development of new drugs. Its unique properties can be leveraged to create molecules with specific biological activities, contributing to the advancement of medicinal chemistry.
Used in Agrochemicals:
2,3,5,6-tetrafluoro-4-methoxybenzaldehyde is also utilized in the production of agrochemicals, where its chemical structure can be employed to create compounds with pesticidal or herbicidal properties, enhancing crop protection and yield.
Used in Aromatic Compounds Production:
Due to its strong odor, 2,3,5,6-tetrafluoro-4-methoxybenzaldehyde is used in the creation of various aromatic compounds. It serves as a precursor in the fragrance industry, contributing to the development of new scents and flavorings.
Used in Material Science:
2,3,5,6-tetrafluoro-4-methoxybenzaldehyde has potential applications in the development of new materials. Its unique chemical structure can be incorporated into polymers, coatings, or other materials to impart specific properties, such as enhanced stability or reactivity.
Used as a Research Reagent:
In chemical research, 2,3,5,6-tetrafluoro-4-methoxybenzaldehyde is used as a reagent to explore new reaction pathways and mechanisms. Its fluorinated and methoxylated nature provides a platform for studying the effects of these functional groups on chemical behavior and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 19161-44-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,1,6 and 1 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19161-44:
(7*1)+(6*9)+(5*1)+(4*6)+(3*1)+(2*4)+(1*4)=105
105 % 10 = 5
So 19161-44-5 is a valid CAS Registry Number.

19161-44-5Relevant articles and documents

On the reaction of some 5-polyfluoroaryl-1,2,4-oxadiazoles with methylhydrazine: synthesis of fluorinated indazoles

Palumbo Piccionello, Antonio,Pace, Andrea,Pierro, Paola,Pibiri, Ivana,Buscemi, Silvestre,Vivona, Nicolò

experimental part, p. 119 - 127 (2009/04/07)

The reaction of 5-polyfluoroaryl-1,2,4-oxadiazoles with methylhydrazine has been studied and the synthesis of fluorinated N-methylindazoles has been realized. Rearrangement reactions showed predominantly formation of N(1)-methylindazole regioisomers. Star

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