4162-89-4 Usage
Uses
Used in Organic Synthesis:
5-tert-butyl-2-methyl-1,3-dinitrobenzene is utilized as a reagent in organic synthesis for the preparation of pharmaceuticals and dyes. Its chemical properties make it a valuable intermediate in the creation of a variety of organic compounds.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 5-tert-butyl-2-methyl-1,3-dinitrobenzene is used as a key intermediate in the synthesis of certain medications, contributing to the development of new drugs and therapeutic agents.
Used in Dye Production:
5-tert-butyl-2-methyl-1,3-dinitrobenzene is also employed in the production of dyes, where its chemical structure aids in the creation of colorants for various applications, including textiles and other industrial uses.
Used in Agricultural Chemicals:
5-tert-butyl-2-methyl-1,3-dinitrobenzene serves as an intermediate in the production of agricultural chemicals, playing a role in the development of substances that can protect crops and enhance agricultural productivity.
Used in Explosives Manufacturing:
Additionally, 5-tert-butyl-2-methyl-1,3-dinitrobenzene is used in the manufacturing of explosives, where its chemical properties are harnessed to create materials with specific detonation characteristics.
Safety Measures:
Given its toxic and harmful nature, 5-tert-butyl-2-methyl-1,3-dinitrobenzene requires careful handling and storage. It can cause irritation to the respiratory system and skin, and its potential hazards necessitate the implementation of appropriate safety measures to protect individuals from ingestion, inhalation, or skin absorption.
Check Digit Verification of cas no
The CAS Registry Mumber 4162-89-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,6 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4162-89:
(6*4)+(5*1)+(4*6)+(3*2)+(2*8)+(1*9)=84
84 % 10 = 4
So 4162-89-4 is a valid CAS Registry Number.
4162-89-4Relevant academic research and scientific papers
Synthesis and Prior Misidentification of 4- tert-Butyl-2,6-dinitrobenzaldehyde
Martin, Daniel J.,Mercado, Brandon Q.,Mayer, James M.
, p. 12172 - 12176 (2019/10/02)
Substituted 2,6-dinitrobenzaldehydes are valuable synthetic precursors and have been prepared by several methods. We report here that one reported synthetic method actually forms the 3,5-dinitro isomer, 4-tert-butyl-3,5-dinitrobenzaldehyde, instead of the
On the illusive nature of o-formylazobenzenes: Exploiting the nucleophilicity of the azo group for cyclization to indazole derivatives
Peters, Maike V.,Stoll, Ragnar S.,Goddard, Richard,Buth, Gernot,Hecht, Stefan
, p. 7840 - 7845 (2007/10/03)
(Chemical Equation Presented) Facile rearrangement of azobenzenes is shown to occur in cases where the azo group is placed in the ortho position to carbonyl electrophiles to furnish the indazole skeleton. While this study demonstrates the illusive nature
Metacyclophanes and Related Compounds. Part 16. Preparation of 8-Fluoro-t-butylmetacyclophanes and their Treatment with Aluminium Chloride-Nitromethane in Benzene
Yamato, Takehiko,Arimura, Takashi,Tashiro, Masashi
, p. 1 - 8 (2007/10/02)
The preparation of 8-fluoro-t-butylmetacyclophanes (5) are described.Dithiametacyclophane (3) and metacyclophane bis(sulphones) (4) were obtained as a mixture of transoid and cisoid conformers, but metacyclophanes (5) were exclusively obtained as the transoid conformer after pyrolysis of the sulphones (4).AlCl3-MeNO2-Catalyzed trans-t-butylation of 8-fluoro-16-methyl-5,13-di-t-butylmetacyclophane (5a) in benzene under a variety of conditions faild to give 8-fluoro-16-methylmetacyclophane (32) but, instead, the tetrahydropyrenes (33) and/or (34) were obtained depending upon the conditions used.Internally substituted metacyclophanes were isomerized to the strainless metacyclophanes and these were then oxidized to the tetrahydropyrene (33).
