17700-09-3 Usage
Description
2,3,4-Trichloronitrobenzene, also known as 1,3,5-trichlorobenzene, is an organic compound that exists as a white to light yellow crystalline powder. It is characterized by its needle-like or light yellow fluffy solid appearance. This chemical compound is known for its distinct chemical properties, which make it suitable for various applications across different industries.
Uses
Used in Chemical Synthesis:
2,3,4-Trichloronitrobenzene is used as an intermediate in the chemical synthesis of various organic compounds. Its unique chemical structure allows it to be a versatile building block for the production of dyes, pharmaceuticals, and other specialty chemicals. The compound's reactivity and stability make it an ideal candidate for use in the synthesis of complex molecules.
Used in Dye Manufacturing:
In the dye industry, 2,3,4-trichloronitrobenzene is used as a key component in the production of various types of dyes. Its chemical properties enable it to be easily modified and combined with other compounds to create a wide range of colors and shades. This makes it a valuable resource for the development of new and innovative dyes for various applications, such as textiles, plastics, and printing inks.
Used in Pharmaceutical Industry:
2,3,4-Trichloronitrobenzene is also utilized in the pharmaceutical industry as a starting material for the synthesis of various drugs. Its unique chemical structure allows it to be easily modified and functionalized, making it an ideal candidate for the development of new and effective medications. The compound's versatility and stability contribute to its widespread use in the synthesis of a diverse range of pharmaceutical products.
Used in Pesticide Formulation:
In the agricultural sector, 2,3,4-trichloronitrobenzene is used in the formulation of certain pesticides. Its chemical properties make it an effective active ingredient in controlling pests and protecting crops from damage. The compound's stability and reactivity allow it to be easily incorporated into various pesticide formulations, making it a valuable resource for the development of new and improved pest control products.
Air & Water Reactions
Insoluble in water.
Reactivity Profile
2,3,4-TRICHLORONITROBENZENE is incompatible with strong bases and strong oxidizing agents.
Fire Hazard
Flash point data for 2,3,4-TRICHLORONITROBENZENE are not available. 2,3,4-TRICHLORONITROBENZENE is probably combustible.
Safety Profile
Mutation data reported. Whenheated to decomposition it emits toxic vapors of NOx andClí.
Check Digit Verification of cas no
The CAS Registry Mumber 17700-09-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,7,0 and 0 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17700-09:
(7*1)+(6*7)+(5*7)+(4*0)+(3*0)+(2*0)+(1*9)=93
93 % 10 = 3
So 17700-09-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H2Cl3NO2/c7-3-1-2-4(10(11)12)6(9)5(3)8/h1-2H
17700-09-3Relevant articles and documents
A simple synthesis of 2,3-dichloro-6-nitrobenzonitrile
Trinka,Berecz,Reiter
, p. 679 - 680 (1996)
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Preparation method of 2,3,4-trifluoronitrobenzene
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Paragraph 0028-0030; 0033-0035; 0038-0040; 0043-0045; 0048, (2018/01/03)
The invention discloses a preparation method of 2,3,4-trifluoronitrobenzene and relates to the field of organic synthesis. The preparation method specifically comprises the following steps: firstly, 2,3,4-trichloronitrobenzene is prepared from 1,2,3-trichlorobenzene as a raw material through nitrification and substitution; then KF is added, stirring is performed for dehydration under catalysis of TBAB, a reaction is performed at 180 DEG C, a product is filtered after the reaction, a filtrate is fed into a water-free reactor after being subjected to reduced-pressure distillation, KF is added, reduced-pressure dehydration is performed under catalysis of TBAF, a reaction is performed at 120 DEG C under the ultrasonic power condition of 30 KHZ, a reaction process is tracked by GC, a product is cooled to 70-75 DEG C and filtered after the reaction, a filtrate is distilled for separating DMSO and a product. The method is simple to operate, and the product yield is high.
Preparation method for 3,5,-dichloro-2,4,-difluoroaniline
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Paragraph 0098-0101, (2017/03/08)
The invention relates to the field of organic synthesis, specifically to a preparation method for 3,5,-dichloro-2,4,-difluoroaniline and application thereof. The preparation method for 3,5,-dichloro-2,4,-difluoroaniline provided by the invention comprises the following steps: 1) nitration reaction; 2) reduction reaction; 3) diazotization reaction; 4) nitration reaction; 5) fluorination reaction; and 6) reduction reaction. The preparation method for 3,5,-dichloro-2,4,-difluoroaniline provided by the invention has the following beneficial effects: 1) the method has mild reaction conditions, is stable and controllable, has less active sites, is insusceptible to side reaction, and has good yield and quality in the whole line; and 2) raw materials are cheap and easily available, so cost can be effectively reduced, and energy is saved; meanwhile, the use of chlorine gas is avoided, so the method is environment-friendly.