1513-34-4 Usage
Uses
Used in Organic Synthesis:
4-CHLORO-2-(TRIFLUOROMETHYL)PHENYLHYDRAZINE is used as a building block in organic synthesis for its versatile reactivity and structural features, allowing for the creation of a variety of complex organic molecules.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 4-CHLORO-2-(TRIFLUOROMETHYL)PHENYLHYDRAZINE is utilized as an intermediate in the synthesis of various drugs, contributing to the development of new medicinal compounds with potential therapeutic applications.
Used in Agrochemical Production:
Similarly, in agrochemicals, 4-CHLORO-2-(TRIFLUOROMETHYL)PHENYLHYDRAZINE serves as an intermediate, playing a crucial role in the synthesis of compounds designed to protect crops and enhance agricultural productivity.
Used in Insecticidal Compounds Research:
4-CHLORO-2-(TRIFLUOROMETHYL)PHENYLHYDRAZINE is also used as a reactive intermediate in the research and development of potential insecticidal compounds, aiming to discover new agents for pest control in agriculture and other settings.
Check Digit Verification of cas no
The CAS Registry Mumber 1513-34-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,1 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1513-34:
(6*1)+(5*5)+(4*1)+(3*3)+(2*3)+(1*4)=54
54 % 10 = 4
So 1513-34-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H6ClF3N2/c8-4-1-2-6(13-12)5(3-4)7(9,10)11/h1-3,13H,12H2
1513-34-4Relevant academic research and scientific papers
Antiimplantation Agents: Part I - 1-Arylthiosemicarbazides
Nagarajan, K.,Talwalker, P.K.,Kulkarni, C.L.,Venkateswarlu, A.,Prabhu, S.S.,Nayak, G.V.
, p. 1243 - 1257 (2007/10/02)
Several 1-arylthiosemicarbazides, 2-arylhydrazinothiazolines and 2-arylhydrazinodihydrothiazines have been examined for their antiimplantation activity in rats.Among the active compounds, 4-methyl-1-(3,5-bistrifluoromethylphenyl)thiosemicarbazide (3, C 2696-Go) and the corresponding 4,4-dimethyl (47), ethyl (4), n-butyl (5) and allyl (6) derivatives completely inhibit implantation at doses 10, 3, 20, 20 and 30 mg/kg respectively.The 3,4-dichlorophenyl analogue (32) is effective at a dose of 30 mg/kg. 2-(3,5-Bistrifluoromethylphenyl)hydrazinothiazoline (51) and the corresponding dihydrothiazine (63) show a weaker activity.The biological profile of C 2696-Go has been investigated in detail.It appears to prevent implantation by its antiuterotropic activity and ability to inhibit desiduoma formation.
