111234-64-1 Usage
Uses
Used in Pharmaceutical Industry:
2,6-DICHLORO-3,5-DIFLUORO-4-(TRIFLUOROMETHYL)PHENYLHYDRAZINE is used as a disinfectant and preservative for various pharmaceutical products to ensure their safety and efficacy.
Used in Chemical Industry:
2,6-DICHLORO-3,5-DIFLUORO-4-(TRIFLUOROMETHYL)PHENYLHYDRAZINE is used as a reagent in organic synthesis, contributing to the development of new chemical compounds and materials.
Used in Pesticidal Applications:
2,6-DICHLORO-3,5-DIFLUORO-4-(TRIFLUOROMETHYL)PHENYLHYDRAZINE is used as a pesticide due to its pesticidal properties, helping to control and eliminate harmful pests in agricultural and other settings.
However, it is crucial to handle 2,6-DICHLORO-3,5-DIFLUORO-4-(TRIFLUOROMETHYL)PHENYLHYDRAZINE with care, as it is toxic and can cause irritation to the skin and respiratory system if not handled properly.
Check Digit Verification of cas no
The CAS Registry Mumber 111234-64-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,2,3 and 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 111234-64:
(8*1)+(7*1)+(6*1)+(5*2)+(4*3)+(3*4)+(2*6)+(1*4)=71
71 % 10 = 1
So 111234-64-1 is a valid CAS Registry Number.
111234-64-1Relevant academic research and scientific papers
Derivatives of N-phenylpyrazoles
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, (2008/06/13)
N-Phenylpyrazole derivatives of the formula: STR1 wherein R1 represents cyano, nitro, halogen, acetyl or formyl; R2 represents R5 SO2, R5 SO or R5 S in which R5 is optionally halogen substituted alkyl, alkenyl or alkynyl; R3 represents a hydrogen atom or a group NR6 R7 wherein R6 and R7 each represent hydrogen, alkyl, alkenylalkyl, alkynylalkyl, formyl, optionally halogen substituted alkanoyl, optionally halogen substituted alkoxycarbonyl, or alkoxymethyleneamino, halogen, or R6 and R7 together form a cyclic imide and R4 represents a substituted phenyl group possess arthropodicidal, plant nematocidal, anthelmintic and anti-protozoal properties; their preparation, compositions containing them and their use are described.
