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127371-50-0

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127371-50-0 Usage

General Description

4,5-Difluoro-2-nitrotoluene is a chemical compound that is commonly used in the production of pharmaceuticals, agrochemicals, and other organic compounds. It is a nitro derivative of toluene, containing two fluorine atoms in the 4 and 5 positions and a nitro group in the 2 position. This chemical is known for its strong aromatic odor and is typically found in the form of a colorless to pale yellow liquid. It is considered to be hazardous and can cause irritation to the skin, eyes, and respiratory system upon exposure. In addition, 4,5-difluoro-2-nitrotoluene is also a flammable substance and should be handled and stored with caution.

Check Digit Verification of cas no

The CAS Registry Mumber 127371-50-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,3,7 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 127371-50:
(8*1)+(7*2)+(6*7)+(5*3)+(4*7)+(3*1)+(2*5)+(1*0)=120
120 % 10 = 0
So 127371-50-0 is a valid CAS Registry Number.

127371-50-0 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (H63030)  4,5-Difluoro-2-nitrotoluene, 98%   

  • 127371-50-0

  • 1g

  • 193.0CNY

  • Detail
  • Alfa Aesar

  • (H63030)  4,5-Difluoro-2-nitrotoluene, 98%   

  • 127371-50-0

  • 5g

  • 771.0CNY

  • Detail

127371-50-0Relevant articles and documents

Preparation method of 2,4,5-trifluorophenylacetic acid

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Paragraph 0040-0041; 0078, (2021/05/29)

The invention belongs to the technical field of preparation of drug intermediates, and discloses a preparation method of 2,4,5-trifluorophenylacetic acid, wherein the preparation method comprises the steps: step 1, reacting raw materials, a quaternary ammonium salt catalyst, sulfolane and potassium fluoride to obtain a first intermediate; step 2, carrying out hydrogenation catalytic reaction on the first intermediate to obtain a second intermediate; step 3, carrying out salt forming reaction on the second intermediate and a fluorinating reagent, quenching, and carrying out diazotization reaction on the second intermediate and a sodium nitrite aqueous solution to obtain diazonium salt; step 4, carrying out high-temperature cracking on the diazonium salt, to obtain 2,4,5-trifluorotoluene; and step 5 to step 7, carrying out halogenation, cyanidation and hydrolysis reactions on 2,4,5-trifluorotoluene in sequence, and thus obtaining 2,4,5-trifluorophenylacetic acid. The raw materials adopted by the method are easy to obtain and low in cost, the yield of the corresponding product obtained in each step is high, and large-scale production of the 2,4,5-trifluorophenylacetic acid is facilitated.

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