Category: 64559-06-4

Putta, V. P. Rama Kishore published the artcileThe facile and efficient organocatalytic platform for accessing 1,2,4-selenadiazoles and thiadiazoles under aerobic conditions, SDS of cas: 64559-06-4, the publication is Tetrahedron Letters (2018), 59(10), 904-908, database is CAplus.

The organocatalytic approach towards synthesis of rarely explored 1,2,4-selenadiazole and thiadiazole scaffolds have been devised using corresponding carboxamides as substrates. The transformations were realized using two distinct conditions in the presence of catalytic vitamin B₃ or thiourea under aerobic conditions. Developed methods overcome the associated limitations of previous reported approaches and the desired products were obtained in high yields and selectivity without the formation of toxic side-products.

Tetrahedron Letters published new progress about 64559-06-4. 64559-06-4 belongs to amides-buliding-blocks, auxiliary class Amine,Benzene,Amide,Ether, name is 3-Methoxybenzothioamide, and the molecular formula is C8H9NOS, SDS of cas: 64559-06-4.

Referemce:
https://en.wikipedia.org/wiki/Amide,
Amide – an overview | ScienceDirect Topics

Waisser, K. published the artcileHydrophobic properties of some thiobenzamides, antimycobacterially active compounds, Category: amides-buliding-blocks, the publication is Folia Pharmaceutica Universitatis Carolinae (1998), 23(Suppl.), 114-115, database is CAplus.

HPLC was used to assess the hydrophobic properties of 11 PhCSNH₂ (R = H, 3- and 4-MeO and -Cl, 4-O₂N, 4-Me₂N, 4-Me, 4-MeS, 3,4-Cl₂, 3-Br). A correlation equation was derived for this series of compounds, based on hydrophobic substituent constants calculated for R.

Folia Pharmaceutica Universitatis Carolinae published new progress about 64559-06-4. 64559-06-4 belongs to amides-buliding-blocks, auxiliary class Amine,Benzene,Amide,Ether, name is 3-Methoxybenzothioamide, and the molecular formula is C11H12O4, Category: amides-buliding-blocks.

Referemce:
https://en.wikipedia.org/wiki/Amide,
Amide – an overview | ScienceDirect Topics

Edward, John T. published the artcileApplicability of the HT acidity function to the protonation of thioamides, thioureas, and thioesters, Quality Control of 64559-06-4, the publication is Canadian Journal of Chemistry (1977), 55(12), 2331-5, database is CAplus.

The protonation of eleven thioamides, five thioureas, and four thionbenzoates in aqueous sulfuric acid follows the HT acidity function. Protonation constants pKTH+ obtained by use of HT agreed fairly well with pKTH+ values obtained by the Bunnett-Olsen method, but less well with those obtained by the Marziano-Cimino-Passerini procedure. Linear free energy relation of pKTH+ values are discussed.

Canadian Journal of Chemistry published new progress about 64559-06-4. 64559-06-4 belongs to amides-buliding-blocks, auxiliary class Amine,Benzene,Amide,Ether, name is 3-Methoxybenzothioamide, and the molecular formula is C8H9NOS, Quality Control of 64559-06-4.

Referemce:
https://en.wikipedia.org/wiki/Amide,
Amide – an overview | ScienceDirect Topics

Czaplewski, Lloyd G. published the artcileAntibacterial alkoxybenzamide inhibitors of the essential bacterial cell division protein FtsZ, Synthetic Route of 64559-06-4, the publication is Bioorganic & Medicinal Chemistry Letters (2009), 19(2), 524-527, database is CAplus and MEDLINE.

3-Methoxybenzamide is a weak inhibitor of the essential bacterial cell division protein FtsZ. Exploration of the structure-activity relationships of 3-methoxybenzamide analogs led to the identification of potent anti-staphylococcal compounds

Bioorganic & Medicinal Chemistry Letters published new progress about 64559-06-4. 64559-06-4 belongs to amides-buliding-blocks, auxiliary class Amine,Benzene,Amide,Ether, name is 3-Methoxybenzothioamide, and the molecular formula is C8H9NOS, Synthetic Route of 64559-06-4.

Referemce:
https://en.wikipedia.org/wiki/Amide,
Amide – an overview | ScienceDirect Topics

Drsata, J. published the artcileBiological side-effects of potential antituberculotic agents. XIII. Use of serum aspartate aminotransferase for the examination of organ toxicity of thiobenzamides, Formula: C8H9NOS, the publication is Cesko-Slovenska Farmacie (1988), 37(6), 243-5, database is CAplus and MEDLINE.

Ten title compounds (I; R¹ = H, 4-Br, 3-Cl, 4-Cl, 3-Me, 4-Me, 3-MeO, 4-MeO, 4-NMe₂; R² = H, 4-Cl) were screened for hepatotoxicity as indicated by blood serum levels of aspartate aminotransferase (AST). An equation is derived relating the values of Hammett’s constants for I and log AST. The hepatotoxicity of I decreases with an increase in the value of Hammett’s constant

Cesko-Slovenska Farmacie published new progress about 64559-06-4. 64559-06-4 belongs to amides-buliding-blocks, auxiliary class Amine,Benzene,Amide,Ether, name is 3-Methoxybenzothioamide, and the molecular formula is C8H9NOS, Formula: C8H9NOS.

Referemce:
https://en.wikipedia.org/wiki/Amide,
Amide – an overview | ScienceDirect Topics

Drsata, J. published the artcileBiological side-effects of potential antituberculotic agents. XIII. Use of serum aspartate aminotransferase for the examination of organ toxicity of thiobenzamides, Formula: C8H9NOS, the publication is Cesko-Slovenska Farmacie (1988), 37(6), 243-5, database is CAplus and MEDLINE.

Ten title compounds (I; R¹ = H, 4-Br, 3-Cl, 4-Cl, 3-Me, 4-Me, 3-MeO, 4-MeO, 4-NMe₂; R² = H, 4-Cl) were screened for hepatotoxicity as indicated by blood serum levels of aspartate aminotransferase (AST). An equation is derived relating the values of Hammett’s constants for I and log AST. The hepatotoxicity of I decreases with an increase in the value of Hammett’s constant

Cesko-Slovenska Farmacie published new progress about 64559-06-4. 64559-06-4 belongs to amides-buliding-blocks, auxiliary class Amine,Benzene,Amide,Ether, name is 3-Methoxybenzothioamide, and the molecular formula is C8H9NOS, Formula: C8H9NOS.

Referemce:
https://en.wikipedia.org/wiki/Amide,
Amide – an overview | ScienceDirect Topics

Czaplewski, Lloyd G. published the artcileAntibacterial alkoxybenzamide inhibitors of the essential bacterial cell division protein FtsZ, Synthetic Route of 64559-06-4, the publication is Bioorganic & Medicinal Chemistry Letters (2009), 19(2), 524-527, database is CAplus and MEDLINE.

3-Methoxybenzamide is a weak inhibitor of the essential bacterial cell division protein FtsZ. Exploration of the structure-activity relationships of 3-methoxybenzamide analogs led to the identification of potent anti-staphylococcal compounds

Bioorganic & Medicinal Chemistry Letters published new progress about 64559-06-4. 64559-06-4 belongs to amides-buliding-blocks, auxiliary class Amine,Benzene,Amide,Ether, name is 3-Methoxybenzothioamide, and the molecular formula is C8H9NOS, Synthetic Route of 64559-06-4.

Referemce:
https://en.wikipedia.org/wiki/Amide,
Amide – an overview | ScienceDirect Topics