863870-86-4 Usage
Description
2-Chloro-3-fluorophenol is a phenol derivative belonging to the class of phenol compounds, which are aromatic organic compounds with a hydroxyl group directly bonded to an aromatic hydrocarbon group. This specific chemical features chlorine and fluorine substituents and has the molecular formula C6H4ClFO. It is recognized for its role in the synthesis of various products and holds potential in medicinal chemistry and drug development.
Uses
Used in Pharmaceutical and Agrochemical Industries:
2-Chloro-3-fluorophenol is used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, contributing to the development of new drugs and pesticides due to its unique chemical properties.
Used in Dye and Pigment Production:
2-Chloro-3-fluorophenol is utilized as a building block in the production of dyes and pigments, enhancing the color spectrum and performance of these products in various applications.
Used in Organic Compound Manufacturing:
2-Chloro-3-fluorophenol serves as an intermediate in the manufacturing of other organic compounds, playing a crucial role in the creation of diverse chemical products.
Used in Medicinal Chemistry and Drug Development:
Possessing potential applications in the field of medicinal chemistry, 2-Chloro-3-fluorophenol is employed in drug development for its ability to be modified and incorporated into new therapeutic agents.
It is important to handle 2-Chloro-3-fluorophenol with care due to its hazardous nature and potential health risks if not properly managed.
Check Digit Verification of cas no
The CAS Registry Mumber 863870-86-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,3,8,7 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 863870-86:
(8*8)+(7*6)+(6*3)+(5*8)+(4*7)+(3*0)+(2*8)+(1*6)=214
214 % 10 = 4
So 863870-86-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H4ClFO/c7-6-4(8)2-1-3-5(6)9/h1-3,9H
863870-86-4Relevant articles and documents
Approaches to the synthesis of 2,3-dihaloanilines. Useful precursors of 4-functionalized-1 H-indoles
Guilarte, Veronica,Castroviejo, M. Pilar,Garcia-Garcia, Patricia,Fernandez-Rodriguez, Manuel A.,Sanz, Roberto
, p. 3416 - 3437 (2011/06/28)
2,3-Dihaloanilines have been proved as useful starting materials for synthesizing 4-halo-1H-indoles. Subsequent or in situ functionalization of the prepared haloindoles allows the access to a wide variety of 2,4- or 2,3,4-regioselectively functionalized indoles in good overall yields. As no efficient synthetic routes to 2,3-dihaloanilines have been described in the literature, different approaches to the preparation of these 1,2,3-functionalized aromatic precursors are now presented. The most general one involves a Smiles rearrangement from the corresponding 2,3-dihalophenols and allows the preparation of 2,3-dihaloanilides in a straightforward and synthetically useful manner.
