863870-86-4 Usage
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
experimental part, 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.
A new and efficient synthesis of 4-functionalized benzo[6]furans from 2,3-dihalophenols
Sanz, Roberto,Castroviejo, M. Pilar,Fernandez, Yolanda,Fananas, Francisco J.
, p. 6548 - 6551 (2007/10/03)
Tandem Sonogashira coupling/5-endo-dig cyclization reactions on 2,3-dihalophenols suppose a straightforward entry to 4-halobenzo[b]furans, which can be easily transformed into 4-functionalized benzo[b]furans, that are difficult to synthesize by other proc
