192750. lajstromszámú szabadalom • Hatóanyagként n-fenil-karbamát-származékokat tartalmazó fungicid készítmények és eljárás a hatóanyagok előállítására
23 192750 24 A vegyü let sorszáma X Y R1 R2 z Fizikai állandó 160-CH=CHz-OC2H5-C2H5-CH(CH3)2 0 op.: 127,5-128,5 °C 161-CH2CH2CH2CH3-OC2H5-C2H5-CH(CH3)2 0 op.: 76-77 °C 162-OCH3-OCH3-CH3-CH(CH3)2 0 op.: 121,5-122,5 °C 163-OCH3-OCH3-C2H5-CH(CH3)2 0 op.: 163-164,5 °C 164-OCH3-OCH3-C2H5-CH2CH=CHCH3 0 op.: 112,5-113,5 °C 165-OCH3-OCH3-C2H5-CH(CH)3--ciklopropil 0 op.: 138 °C (bomlik) 166-OCH3-OC2H5-C2H5-CH(CH3>2 0 op.: 124-125 °C 167-OC2H5-OC2H5-C2H5-CH(CH3)2 0 op.: 147-149 °C 168-CH2OCH3-OC2H5-C2H5-CH(CH3)2 0 op.: 107-108 °C 169-CH2OCH3-OC2H5-C2H5-CH(CH3)-CH20CH3 0 op.: 61-66 °C 170-CH20C2H5-OC2H5-C2H5-CH2CSCCH3 0 op.: 79,5-80,5 °C 171 CH20CHzCH=CH2-OC2H5-C2H5-CH(CH3)-C£CH 0 op.: 68,5-69 °C 172-CH20CH2C=CH-OC2H5-C2H5-CH2CH=CHCH3 0 nD24-0 = 1,5279 173-CH2OCH2CH2F-OC2H5-C2H5-CH2C=CCH2C1 0 nD22-5 = 1,5277 174-CH2OCH3-Cl-C2H5-CH(CH3>2 0 nD19-7 = 1,5221 175-CO-OCH3-OC2H5-C2H5-CH(CH3)2 0 op.: 116-118 °C 176-CO-CO2H5-OC2H5-C2H5-CH2CH=CHCH2C1 0 op.: 64-65 °C 177 CO-OCH2CH=CH2-OC2H5-C2H5-CH(CHs)2 0 op.: 110-111 °C 178-CO-OCH2CH2F-OC2H5-C2H5-CH(CH3)2 0 op.: 118-119 °C 179-CO-OCH2C=CH-OC2H5-C2H5-CH(CH3)2 0 op.: 124-125 °C 180-CH20CH3-CH3-C2H5-CH(CH3)2 0 no17 = 1,5198 181-C=N-OC2H5-C2H5-CH(CH3)2 0 op.: 108,5-109,5 °C 182-C=N-CH3-C2H5-CH(CH3)2 0 nD20 = 1,5265 183-CH2C=N-OC2H5-C2H5-CH(CH3)2 0 op.: 101-103 °C 184-CH2CH2C=N-OC2H5-C2H5-CH(CH3>2 0 no16-7 = 1,5089 185-CH=CHC=N-OC2H5-C2H5-CH(CH3)2 0 op.: 97-100 °C 186-CHO-OC2H5-C2H5-CH(CH3)2 0 op.: 103,5-105 °C 187-CH(OCH3)2-OC2H5-C2H5-CH(CH3)2 0 no17*2 = 1,5145 188-CH(OCzHs)2-OC2H5-C2H5-CH(CH3)2 0 nD11,2 = 1,5072 189 1,3-dioxolán—2—il-OC2H5-C2H5-CH(CH3)2 0 op.: 97-99 °C 190-CH=NOH-OC2H5-C2H5-CH{CH3)2 0 op.: 172-173,5 °C 191-CH=NOCH3-OC2H5-C2H5-CH(CH3)2 0 op.: 110-111,5 °C 192-C=CH-OC2H5-C2H5-CH(CH3)2 0 op.: 154,5-156 °C 193-CHBr-CHzBr-OC2H5-C2H5-CH(CH3)2 0 op.: 111-121 °C 194-CO-NH2-OC2H5-C2H5-CH(CH3>2 0 op.: 187-192 °C 195-CO-NHCH3-OC2H5-C2H5-CH(CH3)2 0 op.: 141-143 °C 196-CO-CH3-OC2H5-C2H5-CH(CH3)2 0 op.: 88-90 °C 197-CH2OH-OC2H5-C2H5-CH(CH3)2 0 op.: 117-118 °C 198-CHzOH-OC2H5-C2H5-CH(CH3)-C2H5 0 op.: 86-87,5 °C 199-CH3-CH3-C2H5-C2H5 s no20 = 1,5623 200-CH3-CH3-C2H5-CH(CH3>2 s op.: 73,5-75 °C 201-OC2HS-Cl-C2H5-CH(CH3)2 s op.: 70-71,5 “C 202-OC2H5-Cl-C2H5-CH(CH3)-C2H5 s op.: 80,5-81,5 °C 203-OC2H5-CH3-C2H5-CzHs s op.: 84,5-85,5 °C 204-OC2H5-CH3-C2H5-CH(CH3)2 s op.: 71-72 °C 205-OC2H5-CH3-CzHs-CH(CH3)-C2Hs s op.: 84,5-85,5 °C 206-CH3-CH3-CH3-CH(CH3)-C=CH 0 op.: 67,5-68,5 °C 207-CH3-CH3-CH3-CH(CH2CH3)-C=CH 0 no25 = 1,5269 208-CH2OCH3-CH3-C2H5-CH(CH3)2 0 nD18-5 = 1,5132 209-CH2OCH3-CH3-C2H5-CH3 0 no17 = 1,5219 210-OCH3-CH20CH3-C2H5-CH(CH3)2 0 op.: 90-91,5 °C 211-OCH3-CH20CH3-C2H5-CH(CH3)-CH20CH3 0 no25'2 = 1,5121 212-CH2OCH3-Cl-CH2=CH2-CH(CH3)2 0 no25’0 = 1,5269 213-CH2OCH3-Cl-CH2C=CH-CH(CH3)2 0 no25'0 = 1,5311 214-CH2OCH3-Cl-CH2CH2F-CH(CH3)2 0 no25-0 = 1,5133 215-CH2OCH3-Cl-C2H5-CH(CH3>-ciklopropil 0 nD25-5 = 1,5270 216-CH2OCH3-Cl-C2H5-CH(CH3l-CH20C6HS 0 nD25-5 = 1,5501 13
