34283-94-8 Usage
Uses
Used in Chemical Synthesis:
1,2,5-Trichloro-3-nitrobenzene is used as an intermediate in the synthesis of dyes and pigments for the coloration of various materials. Its unique chemical structure allows for the creation of a wide range of colored compounds.
Used in Pharmaceutical Production:
1,2,5-Trichloro-3-nitrobenzene is utilized in the production of pharmaceuticals, where its chemical properties contribute to the development of new drugs and medications.
Used in Agricultural Chemicals:
1,2,5-Trichloro-3-nitrobenzene is also employed in the production of agricultural chemicals, where it may be used to create pesticides or other agrochemicals to protect crops and enhance agricultural productivity.
Safety Precautions:
Due to its toxic nature, 1,2,5-Trichloro-3-nitrobenzene should be handled with care to avoid skin, eye, and respiratory system irritation. Proper safety measures, such as wearing protective gear and working in well-ventilated areas, are essential when working with 1,2,5-Trichloro-3-nitrobenzene.
Check Digit Verification of cas no
The CAS Registry Mumber 34283-94-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,2,8 and 3 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 34283-94:
(7*3)+(6*4)+(5*2)+(4*8)+(3*3)+(2*9)+(1*4)=118
118 % 10 = 8
So 34283-94-8 is a valid CAS Registry Number.
34283-94-8Relevant academic research and scientific papers
Synthesis and potent antifungal activity against Candida species of some novel 1H-benzimidazoles
Goeker, Hakan,Alp, Mehmet,Ates-Alagoez, Zeynep,Yildiz, Sulhiye
scheme or table, p. 936 - 948 (2009/12/05)
(Chemical Equation Presented) A series of 47 novel N1-alkylated- 2-aryl-5(6)-substituted-1H-benzimidazoles and their three novel indole analogues were synthesized and evaluated for in vitro antifungal activities against Candida species by the tube dilution method. The results showed that compounds 79 and 80, having pyridine at the position C-2, of benzimidazoles exhibited the greatest activity with MIC values of 6.25-3.12 μg/mL. Indole analogues 108-110 have no inhibitory activity.
Ozone-mediated reaction of polychlorobenzenes and some related halogeno compounds with nitrogen dioxide: A novel non-acid methodology for the selective mononitration of moderately deactivated aromatic systems
Suzuki,Mori,Maeda
, p. 841 - 845 (2007/10/02)
In the presence of ozone and preferably methanesulfonic acid as catalyst, polychlorobenzenes undergo selective mononitration with nitrogen dioxide at low temperatures, giving the corresponding polychloronitrobenzenes, in most cases in nearly quantitative yields.
