19936-64-2 Usage
Type
Synthetic organic compound
Primary uses
Fungicide and antifungal agent, commonly applied to fruits, vegetables, and ornamental plants to prevent the growth of mold, mildew, and other fungal diseases
Mechanism of action
Inhibits the biosynthesis of ergosterol in fungal cells, disrupting their cell membrane and ultimately leading to cell death
Systemic properties
Can be absorbed by the plant and distributed throughout its tissues, providing long-lasting protection against fungal infections
Environmental and health concerns
Potential impact on human health and the environment, leading to its regulation and restricted use in some countries.
Check Digit Verification of cas no
The CAS Registry Mumber 19936-64-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,9,3 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19936-64:
(7*1)+(6*9)+(5*9)+(4*3)+(3*6)+(2*6)+(1*4)=152
152 % 10 = 2
So 19936-64-2 is a valid CAS Registry Number.
19936-64-2Relevant articles and documents
Synthesis, Structure, and Catalytic Hydrogenation Activity of [NO]-Chelate Half-Sandwich Iridium Complexes with Schiff Base Ligands
Lv, Wen-Rui,Li, Rong-Jian,Liu, Zhen-Jiang,Jin, Yan,Yao, Zi-Jian
, p. 8181 - 8188 (2021/05/26)
A series of N,O-coordinate iridium(III) complexes with a half-sandwich motif bearing Schiff base ligands for catalytic hydrogenation of nitro and carbonyl substrates have been synthesized. All iridium complexes showed efficient catalytic activity for the hydrogenation of ketones, aldehydes, and nitro-containing compounds using clean H2 as reducing reagent. The iridium catalyst displayed the highest TON values of 960 and 950 in the hydrogenation of carbonyl and nitro substrates, respectively. Various types of substrates with different substituted groups afforded corresponding products in excellent yields. All N,O-coordinate iridium(III) complexes 1-4 were well characterized by IR, NMR, HRMS, and elemental analysis. The molecular structure of complex 1 was further characterized by single-crystal X-ray determination.
