1422-53-3 Usage
Description
2-Bromo-4-fluorotoluene is an organic compound that features a bromine and a fluorine atom attached to a toluene molecule. It is a colorless to light yellow liquid and is known for its unique chemical properties that make it suitable for various applications in different industries.
Uses
Used in Pharmaceutical Industry:
2-Bromo-4-fluorotoluene is used as an intermediate in the synthesis of pharmaceutical compounds for its ability to be chemically modified and incorporated into drug molecules.
Used in Chemical Synthesis:
2-Bromo-4-fluorotoluene is used as a building block in the preparation of various organic compounds, such as the meta-fluoro analog, (tris(5-fluoro-2-methylphenyl)phosphane, F-TOTP), due to its reactive bromine and fluorine atoms that can be further functionalized.
Used in Material Science:
2-Bromo-4-fluorotoluene may be utilized in the development of new materials, such as polymers or coatings, that require specific chemical and physical properties imparted by the bromine and fluorine atoms.
Used in Research and Development:
As a versatile organic compound, 2-Bromo-4-fluorotoluene is used in research and development for exploring new reactions, understanding chemical behavior, and developing novel applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 1422-53-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,2 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1422-53:
(6*1)+(5*4)+(4*2)+(3*2)+(2*5)+(1*3)=53
53 % 10 = 3
So 1422-53-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H6BrF/c1-5-6(8)3-2-4-7(5)9/h2-4H,1H3
1422-53-3Relevant articles and documents
Preparation of biaryl compounds
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, (2008/06/13)
A method for the preparation of biaryl compounds is disclosed which comprises contacting an aromatic halide in the presence of a catalyst comprising zerovalent nickel, a bidentate phosphorus-containing coordinating ligand and a reducing metal in a polar, aprotic solvent system for a time and under conditions suitable for the formation of biaryl compound.