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. 2017 May 20;42(2):25–31. doi: 10.1584/jpestics.D16-100

Table 3. Activities and physical parameters of tolprocarb derivatives (part B).

No. A R1 R2 PKS-A IC50(μM) MBI-A MIC (ppm) RBC-E Index Tm (°C) AlogP
1 CH2CF3 i-Pr H 3.05×10−2 0.2 8 132.2 3.51
2 i-Pr i-Pr H 9.75×10−2 1 5 132.4 3.30
17 CH2CF3 H H 2.01×10−1 5 2 169.3 2.23
18 i-Pr CH3 CH3 1.39 500 2 110.0 2.50
19 CH2CF3 H i-Pr >100 500 2 129.0 3.51
20 i-Pr H i-Pr >100 >500 1 159.7 3.30
21 CH2CF3 n-Pr H 6.93×10−2 1 3 170.8 3.51
22 CH2CF3 t-Bu H 2.82×10−2 0.2 12 101.0 4.02
23 CH2CF3 i-Bu H 4.68×10−1 100 1 147.5 3.84
24 CH2CF3 c-Hex H 4.32×10−2 1 3 155.0 4.20
25 CH2CF3 COOCH3 H 2.87×10−2 1 3 139.3 2.12
26 CH2CF3 CH2SCH3 H 3.03×10−1 5 2 153.0 2.58
27 i-Pr CH2SCH3 H 1.65 500 2 162.2 2.36
28 CH2CF3 CH2SOCH3 H 1.04×101 >500 0 153.7 1.44
29 i-Pr CH2SOCH3 H >100 >500 0 192.7 1.22