2H-1-Benzopyran-3-carboxaldehyde, 4-chloro-6-fluoro-


Chemical Name: 2H-1-Benzopyran-3-carboxaldehyde, 4-chloro-6-fluoro-
CAS Number: 105799-69-7
Product Number: AG003L5T(AGN-PC-0JVOQ2)
Synonyms:
MDL No:
Molecular Formula: C10H6ClFO2
Molecular Weight: 212.6048

Identification/Properties


Properties
MP:
84-88 °C(lit.)
BP:
332.6°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
212.604g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
212.004g/mol
Monoisotopic Mass:
212.004g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
277
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


Request for Quotation


Customer Feedback


Chemical Structure



4-Chloro-6-fluoro-2H-chromene-3-carbaldehyde, also known as $name$, is a versatile chemical compound commonly used in chemical synthesis processes. Its unique structure and properties make it an excellent reagent for various synthetic applications.This compound is often employed as a key intermediate in the synthesis of biologically active molecules and pharmaceutical compounds. Its reactive aldehyde group allows for selective functionalization and modification, enabling the creation of complex organic scaffolds. Additionally, the presence of the chloro and fluoro substituents provides opportunities for further derivatization to tailor the compound for specific synthetic pathways.In organic synthesis, 4-Chloro-6-fluoro-2H-chromene-3-carbaldehyde serves as a valuable building block for the construction of heterocyclic compounds, such as benzopyrans and chromenes, which are widely found in natural products and drug molecules. Its ability to participate in various types of chemical reactions, including nucleophilic additions and condensations, makes it a versatile tool for the preparation of diverse chemical structures.Furthermore, the chromene core of this compound offers interesting electronic and spectroscopic properties that can be utilized in materials science and the development of new functional materials. By harnessing the synthetic potential of 4-Chloro-6-fluoro-2H-chromene-3-carbaldehyde, chemists can access a wide range of molecular diversity and explore innovative pathways in chemical synthesis.