140923-17-7 Usage
Description
Iprovalicarb is a diastereoisomeric mixture consisting of equimolar amounts of L-(R)and L-(S)-iprovalicarb. It is a systemic fungicide that is specific to oomycetes, which are a group of pathogenic fungi. IPROVALICARB is utilized in the agricultural industry to protect crops from fungal infections.
Used in Agricultural Industry:
Iprovalicarb is used as a fungicide for the control of pathogenic fungi from the oomycetes class in various crops. It is particularly effective in protecting grapes, potatoes, tomatoes, and other crops from fungal infections, ensuring a healthy yield and reducing the need for alternative, potentially harmful treatments.
Used in Crop Protection:
Iprovalicarb is used as a systemic fungicide for the protection of crops against oomycete infections. Its specificity to oomycetes allows for targeted treatment of these pathogens without causing harm to beneficial organisms or the environment. This targeted approach helps maintain the ecological balance while providing effective control of fungal diseases in agricultural settings.
Check Digit Verification of cas no
The CAS Registry Mumber 140923-17-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,9,2 and 3 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 140923-17:
(8*1)+(7*4)+(6*0)+(5*9)+(4*2)+(3*3)+(2*1)+(1*7)=107
107 % 10 = 7
So 140923-17-7 is a valid CAS Registry Number.
InChI:InChI=1/C18H28N2O3/c1-11(2)16(20-18(22)23-12(3)4)17(21)19-14(6)15-9-7-13(5)8-10-15/h7-12,14,16H,1-6H3,(H,19,21)(H,20,22)/t14-,16?/m0/s1
140923-17-7Relevant articles and documents
Design, synthesis, and fungicidal activities of imino diacid analogs of valine amide fungicides
Sun, Man,Yang, Hui-Hui,Tian, Lei,Li, Jian-Qiang,Zhao, Wei-Guang
, p. 5729 - 5731 (2015)
The novel imino diacid analogs of valine amides were synthesized via several steps, including the protection, amidation, deprotection, and amino alkylation of valine, with the resulting structures confirmed by 1H and 13C NMR and HRMS. Bioassays showed that some of these compounds exhibited good fungicidal activity. Notably, isopropyl 2-((1-((1-(3-fluorophenyl)ethyl)amino)-3-methyl-1-oxobutan-2-yl)amino)propanoate 5i displayed significant levels of control, at 50%, against Erysiphe graminis at 3.9 μM as well as a level of potency very similar to the reference azoxystrobin, which gave 60% activity at this concentration. The present work demonstrates that imino diacid analogs of valine amides could be potentially useful key compounds for the development of novel fungicides against wheat powdery mildew.
