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260443-89-8

  • Product Name:NSC-703786
  • Molecular Formula:C14H11FN2S
  • Molecular Weight:258.319
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Product Details

Purity:99%

Chinese Factory Supply Wholesale NSC-703786 260443-89-8 with Cheap Price

  • Molecular Formula:C14H11FN2S
  • Molecular Weight:258.319
  • PSA:67.15000 
  • LogP:4.57420 

260443-89-8 Relevant articles

Recyclable copper-catalyzed cyclization of o-haloanilides and metal sulfides: An efficient and practical access to substituted benzothiazoles

Cai, Mingzhong,Hao, Wenyan,Huang, Wencheng,Ye, Qian

, (2022/01/19)

An efficient heterogeneous copper-cataly...

Antitumour benzothiazoles. Part 32: DNA adducts and double strand breaks correlate with activity; Synthesis of 5F203 hydrogels for local delivery

Stone, Erica L.,Citossi, Francesca,Singh, Rajinder,Kaur, Balvinder,Gaskell, Margaret,Farmer, Peter B.,Monks, Anne,Hose, Curtis,Stevens, Malcolm F.G.,Leong, Chee-Onn,Stocks, Michael,Kellam, Barrie,Marlow, Maria,Bradshaw, Tracey D.

supporting information, p. 6891 - 6899 (2015/11/11)

Potent, selective antitumour AhR ligands...

Bioactivation of fluorinated 2-aryl-benzothiazole antitumor molecules by human cytochrome P450s 1A1 and 2W1 and deactivation by cytochrome P450 2S1

Wang, Kai,Guengerich, F. Peter

, p. 1740 - 1751 (2012/11/07)

Both 2-(4-amino-3-methylphenyl)-5-fluoro...

Efficient and economical access to substituted benzothiazoles: Copper-catalyzed coupling of 2-haloanilides with metal sulfides and subsequent condensation

Ma, Dawei,Xue, Peng,Jiang, Yongwen,Xie, Siwei,Zhang, Xiaojing,Dong, Jinhua

supporting information; experimental part, p. 4222 - 4225 (2009/11/30)

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260443-89-8 Process route

4-amino-N-(5-fluoro-2-iodophenyl)-3-methylbenzamide

4-amino-N-(5-fluoro-2-iodophenyl)-3-methylbenzamide

4-(5-fluorobenzothiazol-2-yl)-2-methylphenylamine
260443-89-8

4-(5-fluorobenzothiazol-2-yl)-2-methylphenylamine

Conditions
Conditions Yield
4-amino-N-(5-fluoro-2-iodophenyl)-3-methylbenzamide; With sodiumsulfide nonahydrate; In N,N-dimethyl-formamide; at 80 ℃; for 12h; Schlenk technique; Sealed tube;
With hydrogenchloride; In N,N-dimethyl-formamide; at 20 ℃; for 10h;
71%
4-amino-N-(5-fluoro-2-iodophenyl)-3-methylbenzamide; With copper(l) iodide; sodiumsulfide nonahydrate; In N,N-dimethyl-formamide; at 80 ℃; for 12h;
With hydrogenchloride; In N,N-dimethyl-formamide; at 20 ℃;
69%
5-fluoro-2-(3-methyl-4-nitrophenyl)benzothiazole
260443-96-7

5-fluoro-2-(3-methyl-4-nitrophenyl)benzothiazole

4-(5-fluorobenzothiazol-2-yl)-2-methylphenylamine
260443-89-8

4-(5-fluorobenzothiazol-2-yl)-2-methylphenylamine

Conditions
Conditions Yield
With tin(II) chloride hydrate; In ethanol; for 3h; Reflux;
48%
With tin(ll) chloride; In ethanol; for 2h; Heating;
45%
With tin(ll) chloride; In ethanol; Heating;

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