
CAS Name: 3-Chloro-5-[[[[(4,6-dimethoxy-2-pyrimidinyl)amino]carbonyl]amino]sulfonyl]-1-methyl-1H-pyrazole-4-carboxylic acid methyl ester
Additional Names: methyl 3-chloro-5-(4,6-dimethoxypyrimi...
Literature References: Sulfonylurea herbicide. Prepn: S. Yamamoto et al., JP Kokai 85 208977; eidem, US 4668277 (1985, 1987 both to Nissan); S. Yamamoto et al., ACS Symp. Ser. 504, 34 (1992). Physical properties and field trials in corn: K. Suzuki et al., Brighton Crop Prot. Conf. - Weeds 1991, 31. Field trials in landscape plants: R. T. Hurt, W. K. Vencill, J. Environ. Hort. 12, 135 (1994).
CAS Name: 2-[[[[(4,6-Dimethoxy-2-pyrimidinyl)amino]carbonyl]amino]sulfonyl]-4-[[(methylsulfonyl)amino]methyl]benzoic acid methyl ester
Additional Names: methyl 2-[3-(4,6-dimethoxypyrimidin-2-yl...
Literature References: Sulfonylurea herbicide; acetolactate synthase inhibitor. Prepn: K. Lorenz et al., WO 9510507; eidem US 5648315 (1995, 1997 both to Hoechst Schering AgrEvo). Comprehensive description: E. Hacker et al., BCPC Conf. - Weeds 2001, 43-48. Greenhouse trial of combination with iodosulfuron-methyl-sodium in winter wheat: W. A. Bailey et al., Weed Sci. 51, 515 (2003).
CAS Name: N-[[(4,6-Dimethoxy-2-pyrimidinyl)amino]carbonyl]-3-(ethylsulfonyl)-2-pyridinesulfonamideTrademarks: Matrix (DuPont); Titus (DuPont)
Percent Composition: C 38.97%, H 3.97%, N 16.23%, O...
Literature References: Sulfonylurea herbicide; blocks branched-chain amino acid synthesis by inhibiting the plant enzyme, acetolactate synthase. Prepd (not claimed): P. H. Liang, US 4774337 (1988 to DuPont); and use in herbicidal mixtures: idem, EP 341011 (1989 to DuPont), C.A. 113, 6360 (1990). Comprehensive description: H. L. Palm et al., Brighton Crop Prot. Conf. - Weeds 1989, 23-28. HPLC, TLC determn and environmental fate: G. E. Schneiders et al., J. Agric. Food Chem. 41, 2402 (1993). Field trials in potatoes: C. V. Eberlein et al., Weed Technol. 8, 428 (1994).
CAS Name: N-[[(1-Methylethyl)amino]carbonyl]-4-[(3-methylphenyl)amino]-3-pyridinesulfonamide
Additional Names: 1-isopropyl-3-[(4-m-toluidino-3-pyridyl)sulfonyl]urea; 3-isopropylcarbamylsulfonam...
Literature References: Sulfonylurea loop diuretic. Prepn: J. E. DeLarge et al., DE 2516025; eidem, US 4018929 (1975, 1977 both to A. Christiaens, S.A.); J. DeLarge, C. L. Lapiere, Ann. Pharm. Fr. 36, 369 (1978). Pharmacokinetics in humans: M. Lesne et al., Int. J. Clin. Pharmacol. Ther. Toxicol. 20, 382 (1982). Preliminary evaluation in acute heart failure: R. Stroobandt et al., Arch. Int. Pharmacodyn. 260, 151 (1982). Clinical pharmacology: D. C. Brater et al., Clin. Pharmacol. Ther. 42, 187 (1987). Series of articles on pharmacology, mode of action and renal effects in animals: Arzneim.-Forsch. 35, 1520-1541 (1985); on pharmacology, pharmacokinetics and clinical studies: Eur. J. Clin. Pharmacol. 31, Suppl., 1-55 (1986); Arzneim.-Forsch. 38, 143-214 (1988). Clinical comparison with furosemide, q.v., in congestive heart failure: J. Cosin et al., Eur. J. Heart Fail. 4, 507 (2002).
CAS Name: 2-[[[[(4,6-Dimethoxy-2-pyrimidinyl)amino]carbonyl]amino]sulfonyl]-6-(trifluoromethyl)-3-pyridinecarboxylic acid methyl ester
Additional Names: methyl 2-[(4,6-dimethoxypyrimidin-2-ylca...
Literature References: Sulfonylurea postemergent herbicide which inhibits acetolactate synthetase. Prepn: T. A. Andrea, P. H. T. Liang, EP 502740; eidem, US 5393734 (1992, 1995 both to Du Pont). Description of chemical and biological activities: S. R. Teaney et al., Brighton Crop Prot. Conf. - Weeds 1995, 49. Metabolism and selectivity: M. K. Koeppe et al., Pestic. Biochem. Physiol. 59, 105 (1998). LC determn in soil and water: C. R. Powley, P. A. de Bernard, J. Agric. Food Chem. 46, 514 (1998). Environmental fate: S. K. Singles et al., Pestic. Sci. 55, 288 (1999).
CAS Name: 3-Ethyl-2,5-dihydro-4-methyl-N-[2-[4-[[[[(trans-4-methylcyclohexyl)amino]carbonyl]amino]sulfonyl]phenyl]ethyl]-2-oxo-1H-pyrrole-1-carboxamide
Additional Names: N-[4-[2-(3-ethyl-4-meth...
Literature References: Sulfonylurea. Prepn: R. Weyer et al., DE 2951135; eidem, US 4379785 (1981, 1983 both to Hoechst). Synthesis: R. Weyer, V. Hitzel, Arzneim.-Forsch. 38, 1079 (1988). Pharmacology: K. Geisen, ibid., 1120. Effects on insulin and glucagon secretion: V. Leclercq-Meyer et al., Biochem. Pharmacol. 42, 1634 (1991). HPLC determn in biological fluids: K. H. Lehr, P. Damm, J. Chromatogr. 526, 497 (1990). Clinical pharmacokinetics: K. Ratheiser et al., Arzneim.-Forsch. 43, 856 (1993). Toxicity study: U. Schollmeier et al., ibid. 1038. Series of articles on pharmacology and clinical efficacy: Diabetes Res. Clin. Pract. 28 Suppl., S115-S149 (1995).
CAS Name: S-(3-Hydroxy-1,1-dimethylpropyl)-L-cysteine
Additional Names: L-3-[(3-hydroxy-1,1-dimethylpropyl)thio]alanine; (-)-felinine
Percent Composition: C 46.35%, H 8.27%, N 6.76%, O 23.16...
Literature References: Sulfur containing amino acid; occurs as L-(-)-form in cat urine. Isoln: R. G. Westall, Biochem. J. 55, 244 (1953). Synthesis of (±)-felinine: S. Trippett, J. Chem. Soc. 1957, 1929; of (-)-felinine: H. Eggerer, Ann. 657, 212 (1962); A. Schöberl et al., Ber. 101, 373 (1968).
Additional Names: Thiofeed
Literature References: Sulfur containing peptide antibiotic complex produced by Streptomyces tateyamensis no. 7906: Miyairi et al., DE 1929355 (1969 to Fujisawa), C.A. 72, 88921w (1970). Consists of the a and b series of thiopeptins A1, A2, A3, A4, and B (major component). Structurally similar to thiostrepton, q.v. Biological and chemical studies: Miyairi et al., Antimicrob. Agents Chemother. 1, 192 (1972). Characterization of thiopeptins B: Miyairi et al., J. Antibiot. 23, 113 (1970); structural studies: Muramatsu et al., ibid. 25, 537 (1972); 30, 383 (1977). Total structures of components: O. D. Hensens, G. Albers-Schönberg, Tetrahedron Lett. 1978, 3649.
CAS Name: 7,7'-(Carbonyldiimino)bis[4-hydroxy-3-[[2-sulfo-4-[(4-sulfophenyl)azo]phenyl]azo]-2-naphthalenesulfonic acid] hexasodium salt
Additional Names: C.I. 35780; C.I. Direct Red 80; Sirius ...
Literature References: Sulphonated tetrakisazo dye. Dye molecules bind parallel to helical native collagen. Water and light stability: J. J. Porter, Text. Res. J. 43, 735 (1973). Spectral study: J. P. Hart, W. F. Smyth, Spectrochim. Acta 36A, 279 (1980). Staining mechanisms: L. Feldskov Nielsen et al., Biotech. Histochem. 73, 71 (1998). Use as stain for collagen: F. Sweat et al., Arch. Pathol. 78, 69 (1964); D. A. Lee et al., J. Mater. Sci.: Mater. Med. 9, 47 (1998).
CAS Name: 2-[[[[[(4,6-Dimethoxy-2-pyrimidinyl)amino]carbonyl]amino]sulfonyl]methyl]benzoic acid methyl ester
Additional Names: methyl 2-[(4,6-dimethoxypyrimidin-2-yl)ureidosulfonylmethyl]benzoa...
Literature References: Sulphonylurea herbicide primarily used on rice and aquatic weeds. Prepn: R. F. Sauers, EP 51466; idem, US 4420325 (1982, 1983 both to DuPont). Conformation study: Y. K. Kang, D. W. Kim, Bull. Korean Chem. Soc. 11, 144 (1990). Environmental persistence: A. Ferrero et al., Mobility Degrad. Xenobiot., Proc. 9th Simp. Pestic. Chem. 1993, 257. HPLC determn in soil: C. Salardi et al., Meded. Fac. Landbouwwet. Univ. Gent 61, 617 (1996). LC determn in rice and crayfish; M. Zhou et al., J. AOAC Int. 79, 791 (1996). Control of aquatic weeds: G. McCorkelle et al., Proc. 9th Aust. Weeds Conf. 1990, 549. Field trials on rice: J. L. Pacheco, C. L. Pope, Proc. West. Soc. Weed Sci. 39, 147 (1986); M. P. Braverman, Weed Technol. 9, 494 (1995).
即日起可免费注册成为会员, 建立企业产品库, 免费上传产品目录, 企业介绍等. 让你的产品直接呈现给客户.
试运营阶段,所有广告业务5折优惠
