101645-12-9 Usage
Description
Benzenamine, 4-[2-(4-pyridinyl)ethenyl]-, (E)-, also known as 4-(4-pyridyl)-2-butenylaniline, is a chemical compound characterized by a benzene ring with an attached amine group and a 4-pyridinyl ethenyl moiety. Benzenamine, 4-[2-(4-pyridinyl)ethenyl]-, (E)serves as a versatile building block in the synthesis of various organic compounds and pharmaceutical drugs, and is utilized in research and development for new materials and chemical processes. Its structural features and properties also suggest potential applications in medicine and pharmacology, although it requires careful handling and adherence to safety protocols due to possible health risks.
Uses
Used in Pharmaceutical Synthesis:
Benzenamine, 4-[2-(4-pyridinyl)ethenyl]-, (E)is used as a key intermediate in the synthesis of pharmaceutical drugs, contributing to the development of new medications with diverse therapeutic applications.
Used in Organic Compound Synthesis:
Benzenamine, 4-[2-(4-pyridinyl)ethenyl]-, (E)is utilized as a building block in the creation of a variety of organic compounds, expanding the scope of chemical research and innovation.
Used in Research and Development:
Benzenamine, 4-[2-(4-pyridinyl)ethenyl]-, (E)is employed in research and development for the exploration of new materials and chemical processes, driving advancements in the chemical industry.
Used in Medical and Pharmacological Applications:
Due to its unique structural features and properties, Benzenamine, 4-[2-(4-pyridinyl)ethenyl]-, (E)may have potential uses in the medical and pharmacological fields, although further research is necessary to fully understand its capabilities and limitations in these areas.
Check Digit Verification of cas no
The CAS Registry Mumber 101645-12-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,6,4 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 101645-12:
(8*1)+(7*0)+(6*1)+(5*6)+(4*4)+(3*5)+(2*1)+(1*2)=79
79 % 10 = 9
So 101645-12-9 is a valid CAS Registry Number.
101645-12-9Relevant articles and documents
A small-molecule chemosensor for the selective detection of 2,4,6-trinitrophenol (TNP)
Pan, Jianting,Tang, Fang,Ding, Aixiang,Kong, Lin,Yang, Longmei,Tao, Xutang,Tian, Yupeng,Yang, Jiaxiang
, p. 191 - 195 (2015)
A pyridine-based small-molecule receptor (L) for the specific recognition of TNP was synthesised and characterised by 1H NMR, 13C NMR and FT-IR spectra, and the optical properties were studied by UV-Vis absorption and PL spectra. The
Inhibitory effect of cytotoxic nitrogen-containing heterocyclic stilbene analogues on VEGF protein secretion and VEGF, hTERT and c-Myc gene expression
Martí-Centelles, Rosa,Murga, Juan,Falomir, Eva,Carda, Miguel,Alberto Marco
supporting information, p. 1809 - 1815 (2015/10/20)
A group of 21 nitrogen-containing heterocyclic stilbene derivatives, prepared by means of Heck coupling reactions, has been investigated for their cytotoxicity as well as their ability to inhibit the production of the vascular endothelial growth factor (VEGF) and the activation of telomerase. The ability of these compounds to inhibit proliferation of two tumoral cell lines (HT-29 and MCF-7) and one non-tumoral cell line (HEK-293) was first determined. Subsequently, we determined the capacity of the compounds to inhibit the secretion of VEGF in the aforementioned cell lines and downregulate the expression of the VEGF, hTERT and c-Myc genes, of which the latter two are involved in controlling the activation of telomerase.
Heterocyclic ethenyloxanilates as orally active antiallergic agents
Grozinger,Sorcek,Oliver
, p. 487 - 491 (2007/10/02)
Ethyl p-(pyrimidin-4-ylethenyl)oxanilate 2 and many substituted derivatives were found to have oral activity in the PCA assay. The pyrimidine moiety was replaced by other heterocycles but only pyrazine and pyridazine retained activity.
