Benzoyl derivatives
Filed: February 26th, 1998 [Granted]
Patent Number: 6054414
R17 R18 R19 n R12 R13 R21 R22 YLM 4.554 CH3 HH 2 CH3 H CH3 H CH— N(CH3)2 H CH3 4.555 CH3 HH 0 CH3 H CH3 H CH— NHOC2H5 H CH3 4.556 CH3 HH 1 CH3 H CH3 H CH— ...
Imidazopyrimidines and imidazopyridines for the treatment of neurological ...
Filed: November 7th, 2001 [Granted]
Patent Number: 6642230
... 369 CH3 SH CH3 OCH3 H CH3 C2H5 CH2OCH3 — 370 CH3 s H CH3 OCH3 H CH3 C2H5 C6H5 — 371 CH3 s H CH3 OCH3 H CH3 C2H5 c-C3H5 — 372 CH3 s H CH3 OCH3 H CH3 C2H5 ...
Herbicidal pyrazolesulfonamides
Filed: August 13th, 1987 [Granted]
Patent Number: 4762550
(R6> R7, R9 = H) H CH3 CH3 OCH3 OCH3 Q-22 (R6, R7, R9 = H) H CH3 H OCH3 OCH3 Q- 22 (R6, R7, R9 = H) H CH3 H CH3 OCH3 Q-23 (R6, R7, R9 = H) H CH3 H CH3 OCH3 ...
Imidazopyrimidinyl and imidazopyri dinyl derivatives
Filed: December 15th, 2000 [Granted]
Patent Number: 7045529
X R2 R3 RaIyl j^aryl2 j^aryB N o C2H5 H CI CHF2 HX CH2 CH3 H CH3 CHF2 H oo C2H5 H CI CHF2 HY CH2 CH3 H CH3 CHF2 H po C2H5 H CI CHF2 H 20 AO CH3 H CH3 CHF2 ...
Substituted oxime ethers, their preparation and their use for controlling ...
Filed: July 15th, 1993 [Granted]
Patent Number: 5358968
R> R2 R3 R4 X B.427 CH2=CH— CH2— 2-CH3— CH2— H CH3 CH B.428 CH3— 0-CH2— CH2— 2- CH3— CH2— H CH3 N B.429 CH3— O— CH2— CH2— 2-CH3— CH2— H CH3 CH B.430 CI— ...
Substituted benzyl oximino compounds
Filed: October 13th, 1999 [Granted]
Patent Number: 6329359
17 TABLE A-continued R2 R3 R4 CH3 2,4-(CH3)2— C6H3 CH3 3j5-F2 — CgELj CH3 3 ... A.68 H CH3 H A.69 H CH3 H A.70 H CH3 H A.71 H CH3 H A.72 H CH3 H A.73 H CH3 ...
Herbicidal pyrazole sulfonamides
Filed: March 16th, 1987 [Granted]
Patent Number: 4715886
... CH3 H CH2=CH2 CH3 CH3 CH H CH3 H CH2=CH2 CH3 OCH3 CH H CH3 H CH2N02 CH3 CH3 CH H CH3 H CH2N02 CH3 OCH3 CH H CH3 H CH2NO1 OCH3 OCH3 CH H CH3 H CH2N02 CH3 ...
Cycloalkyl, lactam, lactone and related compounds, pharmaceutical ...
Filed: February 13th, 2004 [Pending]
Patent Application Number: 10777247
$-CH2CH2— H, H — CH3 — CH3 -4> HS $CH2SCH2— H, H — CH3 — CH3 -4> HS CH3CH2CH(CH3 )— H, H — CH3 — CH3 -4> HS CH3CHCH2CH2CH2 H, H — CH3 — CH3 -4> HS 1 1 ...