129015-69-6 Usage
Uses
Due to the limited information available in the provided materials, specific applications of 1-[5-Chloro-3-(trifluoromethyl)-2-pyridyl]hydrazine are not widely documented in scientific literature. However, based on its classification as a hydrazone, it can be inferred that it may have potential applications in various fields such as:
Used in Chemical Synthesis:
1-[5-Chloro-3-(trifluoromethyl)-2-pyridyl]hydrazine may be used as an intermediate or reagent in the synthesis of other organic compounds, given its unique structure and functional groups.
Used in Pharmaceutical Research:
As a hydrazone derivative, 1-[5-Chloro-3-(trifluoromethyl)-2-pyridyl]hydrazine could be explored for its potential as a pharmaceutical candidate, particularly in the development of new drugs with novel therapeutic properties.
Used in Material Science:
1-[5-Chloro-3-(trifluoromethyl)-2-pyridyl]hydrazine's specific chemical structure may also make it a candidate for use in the development of new materials with unique properties, such as in the fields of polymer chemistry or materials engineering.
Check Digit Verification of cas no
The CAS Registry Mumber 129015-69-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,0,1 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 129015-69:
(8*1)+(7*2)+(6*9)+(5*0)+(4*1)+(3*5)+(2*6)+(1*9)=116
116 % 10 = 6
So 129015-69-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H5ClF3N3/c7-3-1-4(6(8,9)10)5(13-11)12-2-3/h1-2H,11H2,(H,12,13)
129015-69-6Relevant academic research and scientific papers
Reisinger, Ales,Bernhardt, Paul V.,Wentrup, Curt
, p. 246 - 256 (2004)
Several tetrazolo[1,5-a]pyridines/2-azidopyridines undergo photochemical nitrogen elimination and ring expansion to 1,3-diazacyclohepta-1,2,4, 6-tetraenes (7,10,13,16,19,22) as well as ring cleavage to cyanovinylketenimines (8,17,20b) in low temperature Ar matrices. 6,8-Dichlorotetrazolo[1,5-a]pyridine/2-azido-3,5-dichloropridine 6 undergoes ready exchange of the chlorine in position 8 (3) with ROH/RONa. 8-Chloro-6-trifluoromethylletrazolo[1,5-a]pyridine 15 undergoes solvolysis of the CF3 group to afford 8-chloro-6-methoxycarbonyltetrazolo[1,5-a]pyridine 18. Several tetrazolopyridines/2-azidopyridines afford 1H- or 5H-1,3-diazepines in good yields on photolysis in the presence of alcohols or amines (11,14,23,25). 5-Chlorotetrazolo[1,5-a]pyridines/2-azido-6-chloropyridines 21 and 38 undergo a rearrangement to 1H-and 3H-3-cyanopyrroles 27 and 45, respectively. The mechanism of this rearrangement was investigated by 15N-labelling and takes place via transient 1,3-diazepines. The structures of 6,8-dichloro-tetrazolo[1,5-a]pyridine 6T, 6-chloro-8-ethoxytetrazoIo[1,5-a]pyridine 9Tb, dipyrrolylmethane 28, and 2-isopropoxy-4-dimethylamino-5H-1,3-diazepine 25b were determined by X-ray crystallography. In the latter case, this represents the first reported X-ray crystal structure of a 5H-1,3-diazepine.
