615-86-1 Usage
Uses
Used in Pharmaceutical Synthesis:
2,4,5-tribromoaniline is used as a key intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Dye Production:
2,4,5-tribromoaniline serves as a precursor in the production of dyes, playing a crucial role in the creation of colorants for textiles, plastics, and other materials.
Used in Organic Compounds Synthesis:
2,4,5-tribromoaniline is utilized as a building block in the synthesis of a range of organic compounds, expanding the scope of chemical research and applications.
Used in Agricultural Chemical Production:
As an intermediate, 2,4,5-tribromoaniline is involved in the production of agricultural chemicals, aiding in the development of pesticides and other agrochemicals to enhance crop protection and yield.
Used as a Reagent in Organic Synthesis:
2,4,5-tribromoaniline functions as a reagent in various organic synthesis processes, facilitating chemical reactions and the formation of desired products.
Check Digit Verification of cas no
The CAS Registry Mumber 615-86-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 615-86:
(5*6)+(4*1)+(3*5)+(2*8)+(1*6)=71
71 % 10 = 1
So 615-86-1 is a valid CAS Registry Number.
615-86-1Relevant academic research and scientific papers
Synthesis of symmetrical dinitro-and diamino-substituted Troeger's base analogues
Sturala, Jiri,Cibulka, Radek
supporting information, p. 7066 - 7074 (2013/02/21)
This report describes a new synthetic approach to symmetrical diamino-substituted Troeger's base analogues, allowing the synthesis of 1,7-, and 4,10-diamino derivatives with no additional substituents and of 3,9-diamino derivative with methyl groups in the 1-, 4-, 7-and 10-positions. The synthesis uses regioselective nitration of dihalo-substituted-or tetrahalo-substituted Troeger's bases followed either by hydrogenation of the nitro functions accompanied by removal of halogen atoms or alternatively by chemoselective reduction of nitro groups to obtain the dihalo-diamino- substituted Troeger's base analogues. The 2,8-diamino derivatives, not accessible by this approach, can be prepared by Buchwald-Hartwig amination of the 2,8-dibromo-substituted Troeger's bases.
Trihalo monoazo dyestuffs
-
, (2008/06/13)
Monoazo dyes exhibiting excellent wash- and lightfastness and being essentially insensitive to acid having the formula SPC1 Wherein X, X1 and X2 are chlorine or bromine, and M is an alkali metal or hydrogen.
