The chemical substance known as {3-[(1,3-dimethyl-2,4,6-trioxotetrahydro-5(2H)-pyrimidinylidene)methyl]phenoxy}acetic acid, with the CAS number 354562-11-1, is a complex organic compound characterized by its unique structural features. It contains a phenoxy group, which is a phenol derivative where the hydroxyl group is replaced by an ether linkage, and an acetic acid moiety, indicating its acidic properties. The presence of a pyrimidinylidene structure suggests potential biological activity, as pyrimidines are often found in pharmaceuticals and agrochemicals. The compound's trioxo structure indicates multiple carbonyl groups, which can enhance reactivity and influence solubility. Additionally, the dimethyl substitution on the pyrimidine ring may affect its steric and electronic properties, potentially impacting its interactions in biological systems. Overall, this compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry and related fields. However, specific applications and biological activities would require further investigation and empirical data.

{3-[(1,3-dimethyl-2,4,6-trioxotetrahydro-5(2H)-pyrimidinylidene)methyl]phenoxy}acetic acid

354562-11-1: The chemical substance known as {3-[(1,3-dimethyl-2,4,6-trioxotetrahydro-5(2H)-pyrimidinylidene)methyl]phenoxy}acetic acid, with the CAS number 354562-11-1, is a complex organic compound characterized by its unique structural features. It contains a phenoxy group, which is a phenol derivative where the hydroxyl group is replaced by an ether linkage, and an acetic acid moiety, indicating its acidic properties. The presence of a pyrimidinylidene structure suggests potential biological activity, as pyrimidines are often found in pharmaceuticals and agrochemicals. The compound's trioxo structure indicates multiple carbonyl groups, which can enhance reactivity and influence solubility. Additionally, the dimethyl substitution on the pyrimidine ring may affect its steric and electronic properties, potentially impacting its interactions in biological systems. Overall, this compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry and related fields. However, specific applications and biological activities would require further investigation and empirical data.

<p>CDA-IN-1 (Compound vs#2-1) is an inhibitor of chitin deacetylase (CDA) that exhibits antifungal activity. By inhibiting fungal CDA activity, it activates plant immune responses and leads to the accumulation of reactive oxygen species (ROS), hindering fungal growth. At a concentration of 100 μM, CDA-IN-1 achieves inhibition rates of 86.9% on P. xanthii's PxCDA1 and 74.5% on PxCDA2. CDA-IN-1 is applicable in research on fungal plant diseases, such as cucumber powdery mildew and tomato gray mold.</p>

CAS 354562-11-1

{3-[(1,3-dimethyl-2,4,6-trioxotetrahydro-5(2H)-pyrimidinylidene)methyl]phenoxy}acetic acid

CDA-IN-1

Ref: TM-T206164