120940-43-4 Usage
Description
1-METHYL-1-[2-NITRO-4-(TRIFLUOROMETHYL)PHENYL]HYDRAZINE is a hydrazine derivative with the molecular formula C8H9F3N4O2. It features a nitro group and a trifluoromethyl group attached to a phenyl ring, making it a versatile chemical compound with applications in various industries.
Uses
Used in Pharmaceutical Industry:
1-METHYL-1-[2-NITRO-4-(TRIFLUOROMETHYL)PHENYL]HYDRAZINE is used as an intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic effects.
Used in Agrochemical Industry:
1-METHYL-1-[2-NITRO-4-(TRIFLUOROMETHYL)PHENYL]HYDRAZINE is used in the synthesis of agrochemicals, specifically as a precursor for the development of new pesticides. Its properties can contribute to the creation of effective pest control solutions.
Used in Pesticide Development:
1-METHYL-1-[2-NITRO-4-(TRIFLUOROMETHYL)PHENYL]HYDRAZINE has been studied for its potential use as a pesticide. Its chemical structure may offer new possibilities for pest control, enhancing agricultural productivity and crop protection.
However, it is important to note that 1-METHYL-1-[2-NITRO-4-(TRIFLUOROMETHYL)PHENYL]HYDRAZINE has the potential to act as a mutagenic and genotoxic agent. Therefore, precautions should be taken when handling this compound to minimize risks to human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 120940-43-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,9,4 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 120940-43:
(8*1)+(7*2)+(6*0)+(5*9)+(4*4)+(3*0)+(2*4)+(1*3)=94
94 % 10 = 4
So 120940-43-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H8F3N3O2/c1-13(12)6-3-2-5(8(9,10)11)4-7(6)14(15)16/h2-4H,12H2,1H3
120940-43-4Relevant articles and documents
Synthesis of 3-aryl substituted benzo[1,2,5]triazepin-4-ones via intramolecular imine formation
Tomaszewski, Miros?aw J.,Boisvert, Luc,Jin, Shujuan
scheme or table, p. 1435 - 1437 (2009/06/18)
3-Aryl substituted benzo[1,2,5]triazepin-4-ones and their pyrido counterparts have been synthesized in five steps from commercially available starting materials. The key step involves base-induced cleavage of trifluoroacetyl-protected hydrazine intermedia
