19128-48-4 Usage
Uses
Used in Pharmaceutical Industry:
2-BROMO-1-CHLORO-3-NITROBENZENE is used as an intermediate in the synthesis of various pharmaceuticals. Its presence in the molecular structure allows for the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 2-BROMO-1-CHLORO-3-NITROBENZENE is used as a precursor in the production of certain agrochemicals. Its chemical structure contributes to the formulation of effective pesticides and other agricultural chemicals.
Used in Dye Industry:
2-BROMO-1-CHLORO-3-NITROBENZENE is utilized in the dye industry for the creation of various dyes. Its chemical composition plays a role in the color properties and stability of the dyes produced.
Used in Research and Development:
2-BROMO-1-CHLORO-3-NITROBENZENE is employed in research and development processes, particularly in the field of medicinal chemistry. It serves as a valuable compound for studying chemical reactions and exploring new applications in drug discovery.
Check Digit Verification of cas no
The CAS Registry Mumber 19128-48-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,1,2 and 8 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 19128-48:
(7*1)+(6*9)+(5*1)+(4*2)+(3*8)+(2*4)+(1*8)=114
114 % 10 = 4
So 19128-48-4 is a valid CAS Registry Number.
InChI:InChI=1S/C6H3BrClNO2/c7-6-4(8)2-1-3-5(6)9(10)11/h1-3H
19128-48-4Relevant academic research and scientific papers
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.
4 AND 5-Halo substituted 2-indanamine compounds
-
, (2008/06/13)
2-Indanamine compounds having 4 and 5-halo substituents are inhibitors of phenylethanolamine N-methyltransferase.
