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N-(3-fluoro-phenyl)-thiobenzamide is a chemical compound with the molecular formula C13H10FNS. It is a derivative of benzamide, featuring a fluorine atom at the 3-position of the phenyl ring and a thiophene ring attached to the nitrogen atom. N-(3-fluoro-phenyl)-thiobenzamide is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals, particularly as a building block for the development of new molecules with specific biological activities. Its structure allows for a range of chemical modifications, making it a versatile intermediate in organic synthesis. The compound's properties, such as its reactivity and stability, are influenced by the presence of the fluorine atom and the thioamide group, which can affect its electronic and steric characteristics.

1629-24-9

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1629-24-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1629-24-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,2 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1629-24:
(6*1)+(5*6)+(4*2)+(3*9)+(2*2)+(1*4)=79
79 % 10 = 9
So 1629-24-9 is a valid CAS Registry Number.

1629-24-9Relevant academic research and scientific papers

Exogenous Photosensitizer-, Metal-, and Base-Free Visible-Light-Promoted C-H Thiolation via Reverse Hydrogen Atom Transfer

Xu, Ze-Ming,Li, Hong-Xi,Young, David James,Zhu, Da-Liang,Li, Hai-Yan,Lang, Jian-Ping

supporting information, p. 237 - 241 (2019/01/10)

Visible-light-driven, intramolecular C(sp2)-H thiolation has been achieved without addition of a photosensitizer, metal catalyst, or base. This reaction induces the cyclization of thiobenzanilides to benzothiazoles. The substrate absorbs visible light, and its excited state undergoes a reverse hydrogen-atom transfer (RHAT) with 2,2,6,6-tetramethylpiperidine N-oxyl to form a sulfur radical. The addition of the sulfur radical to the benzene ring gives an aryl radical, which then rearomatizes to benzothiazole via RHAT.

Antimycobacterial activity of 3'- and 4'-fluorothiobenzanilides

Waisser,Kunes,Odlerova,Roman,Kubicova,Horak

, p. 193 - 195 (2007/10/03)

On the basis of a preliminary study of the antimycobacterial activity of thiobenzanilides, a group of 3/-fluoro- and 4/fluorothiobenzanilides has been synthesized and tested against Mycobacterium tuberculosis, M. kansasii, M. avium and M. fortuitum. The r

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