Smith, Nicholas D. et al. published their research in Bioorganic & Medicinal Chemistry Letters in 2004 | CAS: 3364-80-5

Thiazole-4-carbaldehyde (cas: 3364-80-5) belongs to thiazole derivatives. Thiazole rings are planar and aromatic. Thiazoles are characterized by larger pi-electron delocalization than the corresponding oxazoles and have therefore greater aromaticity.Various laboratory methods exist for the organic synthesis of thiazoles. For example, 2,4-dimethylthiazole is synthesized from thioacetamide and chloroacetone.Recommanded Product: 3364-80-5

Discovery of highly potent, selective, orally bioavailable, metabotropic glutamate subtype 5 (mGlu5) receptor antagonists devoid of cytochrome P450 1A2 inhibitory activity was written by Smith, Nicholas D.;Poon, Steve F.;Huang, Dehua;Green, Mitchell;King, Christopher;Tehrani, Lida;Roppe, Jeffrey R.;Chung, Janice;Chapman, Deborah P.;Cramer, Merryl;Cosford, Nicholas D. P.. And the article was included in Bioorganic & Medicinal Chemistry Letters in 2004.Recommanded Product: 3364-80-5 This article mentions the following:

Structure-activity relationship studies focused on bio-isosteric replacements of 2-pyridyl resulted in mGlu5 receptor antagonists with reduced inhibition of cytochrome P 450 1A2. This led to highly potent, selective and orally bioavailable 2-imidazolyl tetrazoles such as I that are devoid of cytochrome P 450 inhibitory activity. In the experiment, the researchers used many compounds, for example, Thiazole-4-carbaldehyde (cas: 3364-80-5Recommanded Product: 3364-80-5).

Thiazole-4-carbaldehyde (cas: 3364-80-5) belongs to thiazole derivatives. Thiazole rings are planar and aromatic. Thiazoles are characterized by larger pi-electron delocalization than the corresponding oxazoles and have therefore greater aromaticity.Various laboratory methods exist for the organic synthesis of thiazoles. For example, 2,4-dimethylthiazole is synthesized from thioacetamide and chloroacetone.Recommanded Product: 3364-80-5

Referemce:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica

Li, Yi et al. published their research in Russian Journal of General Chemistry in 2022 | CAS: 3364-80-5

Thiazole-4-carbaldehyde (cas: 3364-80-5) belongs to thiazole derivatives. The higher aromaticity of thiazole is due to delocalization of a lone pair of sulfur electrons across the ring, which is evidenced by chemical shifts of ring hydrogen at δ 7.27 and 8.77 ppm (C2 and C4), indicating diamagnetic ring current. There are numerous natural products that possess a thiazole ring with broad pharmacological activities. Thiamine, also known as vitamin B1, possesses a thiazole ring linked with 2-methylpyrimidine-4-amine as hydrochloride salt.Product Details of 3364-80-5

Synthesis and Antimicrobial Activity of Aurone Derivatives Containing Heterocyclic Substituents was written by Li, Yi;Zhao, Haiqing;Niu, Chao;Aisa, Haji Akber;Hou, Xueling. And the article was included in Russian Journal of General Chemistry in 2022.Product Details of 3364-80-5 This article mentions the following:

A series of aurone compounds with the B ring substituted by different heterocycles has been synthesized. All synthesized compounds have been tested for antibacterial activity. It has been determined that different heterocyclic substituents modulate the antibacterial spectrum of aurones. Indole-substituted aurones display good inhibitory activity against Gram-pos. bacteria. Thiophene-substituted aurones exhibit inhibitory activity against fungi. Aminopyrimidine-substituted aurones exhibit promising inhibitory activity against Gram-neg. bacteria. Authors have determined that 2-arylimidazo[1,2-a]pyridones I (R1 = H, OMe) can be used as a platform for antifungal agents design. In the experiment, the researchers used many compounds, for example, Thiazole-4-carbaldehyde (cas: 3364-80-5Product Details of 3364-80-5).

Thiazole-4-carbaldehyde (cas: 3364-80-5) belongs to thiazole derivatives. The higher aromaticity of thiazole is due to delocalization of a lone pair of sulfur electrons across the ring, which is evidenced by chemical shifts of ring hydrogen at δ 7.27 and 8.77 ppm (C2 and C4), indicating diamagnetic ring current. There are numerous natural products that possess a thiazole ring with broad pharmacological activities. Thiamine, also known as vitamin B1, possesses a thiazole ring linked with 2-methylpyrimidine-4-amine as hydrochloride salt.Product Details of 3364-80-5

Referemce:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica

Smith, Nicholas D. et al. published their research in Bioorganic & Medicinal Chemistry Letters in 2004 | CAS: 3364-80-5

Thiazole-4-carbaldehyde (cas: 3364-80-5) belongs to thiazole derivatives. Thiazole rings are planar and aromatic. Thiazoles are characterized by larger pi-electron delocalization than the corresponding oxazoles and have therefore greater aromaticity.Various laboratory methods exist for the organic synthesis of thiazoles. For example, 2,4-dimethylthiazole is synthesized from thioacetamide and chloroacetone.Recommanded Product: 3364-80-5

Discovery of highly potent, selective, orally bioavailable, metabotropic glutamate subtype 5 (mGlu5) receptor antagonists devoid of cytochrome P450 1A2 inhibitory activity was written by Smith, Nicholas D.;Poon, Steve F.;Huang, Dehua;Green, Mitchell;King, Christopher;Tehrani, Lida;Roppe, Jeffrey R.;Chung, Janice;Chapman, Deborah P.;Cramer, Merryl;Cosford, Nicholas D. P.. And the article was included in Bioorganic & Medicinal Chemistry Letters in 2004.Recommanded Product: 3364-80-5 This article mentions the following:

Structure-activity relationship studies focused on bio-isosteric replacements of 2-pyridyl resulted in mGlu5 receptor antagonists with reduced inhibition of cytochrome P 450 1A2. This led to highly potent, selective and orally bioavailable 2-imidazolyl tetrazoles such as I that are devoid of cytochrome P 450 inhibitory activity. In the experiment, the researchers used many compounds, for example, Thiazole-4-carbaldehyde (cas: 3364-80-5Recommanded Product: 3364-80-5).

Thiazole-4-carbaldehyde (cas: 3364-80-5) belongs to thiazole derivatives. Thiazole rings are planar and aromatic. Thiazoles are characterized by larger pi-electron delocalization than the corresponding oxazoles and have therefore greater aromaticity.Various laboratory methods exist for the organic synthesis of thiazoles. For example, 2,4-dimethylthiazole is synthesized from thioacetamide and chloroacetone.Recommanded Product: 3364-80-5

Referemce:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica