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Indole-3-carboxaldehyde-N1-phenyl thiosemicarbazone is a chemical compound with the molecular formula C16H14N4OS. It is derived from the indole-3-carboxaldehyde structure, which is a key component of the indole family of compounds. indole-3-carboxaldehyde-N1-phenyl thiosemicarbazone is characterized by the presence of a thiosemicarbazone group attached to the nitrogen atom at position 1 of the indole ring. Thiosemicarbazones are known for their ability to form stable complexes with metal ions, making them useful in coordination chemistry and as potential chelating agents. The phenyl group attached to the thiosemicarbazone moiety further influences the compound's reactivity and stability. This specific chemical is of interest in various fields, including pharmaceutical research, where it may be explored for its potential biological activities or as a precursor in the synthesis of more complex molecules.

7274-93-3

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7274-93-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7274-93-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,7 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7274-93:
(6*7)+(5*2)+(4*7)+(3*4)+(2*9)+(1*3)=113
113 % 10 = 3
So 7274-93-3 is a valid CAS Registry Number.

7274-93-3Downstream Products

7274-93-3Relevant academic research and scientific papers

Exploring synthetic and therapeutic prospects of new thiazoline derivatives as aldose reductase (ALR2) inhibitors

Shehzad, Muhammad Tariq,Imran, Aqeel,Hameed, Abdul,Rashida, Mariya al,Bibi, Marium,Uroos, Maliha,Asari, Asnuzilawati,Iftikhar, Shafia,Mohamad, Habsah,Tahir, Muhammad Nawaz,Shafiq, Zahid,Iqbal, Jamshed

, p. 17259 - 17282 (2021)

Inhibition of aldose reductase (ALR2) by using small heterocyclic compounds provides a viable approach for the development of new antidiabetic agents. With our ongoing interest towards aldose reductase (ALR2) inhibition, we have synthesized and screened a

Synthesis, characterization and anti-tubercular activity of substituted thiosemicarbazones and their ni(ii) complexes

Ul Ain, Qurat,Insha, Sheikh,Sharma, Rekha

, p. 3208 - 3214 (2021/05/26)

Complexes of substituted isatin-3-thiosemicarbazones (H2itsc-N1-Me, H1L; H2itsc-N1-Ph, H2L) and substituted indole-3-thiosemicarbazone (HIntsc-N1-Ph, H3L) with Ni (II) and triphenylphoshine of formula, [NiCl(L)(Ph3P)] (anionic form of L = 1L, 1; 2L, 2, 3L, 3) have been synthesized. The ligands and complexes have been characterized using spectroscopic techniques (IR, 1H NMR). 1HNMR of complexes supports binding of thio- ligands in anionic form. All the ligands (H1L - H3L) and their complexes were evaluated for their antitubercular activities. The enhancement in anti-TB activity of ligands on complexation with Ni(II) has been observed.

A thiourea structure unit including shrinking amino aromatic compound and its preparation method and application (by machine translation)

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Paragraph 0119; 0124-0127, (2019/07/10)

The invention relates to the technical field of pharmaceutical chemistry, and in particular relates to a thiourea structure unit including shrinking amino aromatic compound and its preparation method and application. The present invention provides including shrinking amino thiourea structure unit of the aromatic heterocyclic compound with the gastric cancer cells through the inner metal ion chelating form stable complexes, thereby suppressing the MGC803 gastric cancer cell proliferation activity. The results of the embodiment of the display, and the compound 3 - AP compared with, the present invention provides including shrinking amino thiourea structure unit of the aromatic heterocyclic compound to stomach MGC803 has better proliferation inhibitory activity. (by machine translation)

Photochromic behavior and mechanism of indole thiosemicarbazide derivates in amorphous powder, solution and nanofiber

Che, Yuanyuan,Liu, Lang,Zhao, Jianzhang,Yu, Yuming,Zhao, Xianmei

, p. 105 - 110 (2019/05/27)

A series of Schiff bases containing the indole group were synthesized. The compound 2-[(1-methyl-1H-indol-3-yl)methylene] hydrazinecarbothioamide (4) exhibits excellent reversible photochromic properties both in solid?solid state and solution. Moreover, t

Solvent-free synthesis of indole-based thiosemicarbazones under microwave irradiation

Liu, Lingling,Yang, Jie,Zhao, Zhigang,Shi, Peiyu,Liu, Xingli

experimental part, p. 57 - 60 (2010/05/19)

A rapid, effi cient and environmentally friendly methodology has been developed for the synthesis of indole-3-carboxaldehyde thiosemicarbazones by using aluminum oxide as the solid support under microwave assisted solvent-free conditions. Compared with the conventional heating method, this method gave the target products in good yield.

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