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Detail of "173159-57-4"

  • MSDS Download
  • CAS Number:
  • 173159-57-4
  • Name:
  • Benzamide,2-[[[[(4,6-dimethoxy-2-pyrimidinyl)amino]carbonyl]amino]sulfonyl]-4-(formylamino)-N,N-dimethyl-

  • Superlist Name:
  • Foramsulfuron
  • Molecular Structure:
  • Formula:
  • C17H20N6O7S
  • Molecular Weight:
  • 452.44
  • Synonyms:
  • N,N-Dimethyl-2-[[N-[[N-(4,6-dimethoxypyrimidin-2-yl)amino]carbonyl]amino]sulfonyl]-4-formamidobenzamide;Option;Option 35WDG;
  • Density:
  • 1.471 g/cm3

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CAS No.173159-57-4 Foramsulfuron

Assay:98%

Supplier:Hangzhou Dayangchem Co., Ltd. [ China (Mainland)]

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CAS No.173159-57-4 Foramsulfuron

Foramsulfuron

Supplier:Hangzhou Share Chemical Co., Ltd [ China (Mainland)]

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CAS No.173159-57-4 Foramsulfuron

1. Chemical name: 1-(4, 6-dimethoxypyrimidin-2-yl)-3-[2-(dimethylcarbamoyl)-5- formamidophenylsulfonyl]urea 2. Product name: foramsulfuron 3. CAS No.: 173159-57-4 4. Assay: 97% 5. Molecular Formula: C17H20N6O7S 6. Molecular Weight: 452.4 7. 1 kg per Tin 8. Application:

Supplier:beijing jinwuyuan(jwy) technology Co., Ltd. [ China (Mainland)]

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CAS No.173159-57-4 Foramsulfuron

Foramsulfuron

Supplier:NEOCHEMA [ Germany]

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CAS No.173159-57-4 Foramsulfuron

more information,please contact us

Supplier:Interchim S.A. [ Germany]

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CAS No.173159-57-4 Foramsulfuron

95%TC;35%WDG

Supplier:Changzhou Share Chemical Co.,Ltd. [ China (Mainland)]

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CAS No.173159-57-4 Foramsulfuron

Supplier:Changzhou Xinyou co., ltd. [ China (Mainland)]

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CAS No.173159-57-4 Foramsulfuron

Supplier:AccuStandard Inc [ United States]

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CAS No.173159-57-4 Foramsulfuron

Supplier:China Surchem International [ China (Mainland)]

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Reference

Sulfonylurea compositions having enhanced herbicidal effect
Sulfonylurea compositions having enhanced herbicidal effect. Yoshii, Hiroshi; Ishihara, Yoshiaki; Yamada, Ryu; Tsuruta, Tatsuhiko ( Ishihara Sangyo Kaisha, Ltd., Japan). PCT Int. Appl. WO 2005009132 A1 3 Feb 2005, 81 pp. DESIGNATED STATES: W: AE, AG, AL, AM, AT, AU, AZ, BA, BB, BG, BR, BW, BY, BZ, CA, CH, CN, CO, CR, CU, CZ, DE, DK, DM, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, HR, HU, ID, IL, IN, IS, KE, KG, KP, KR, KZ, LC, LK, LR, LS, LT, LU, LV, MA, MD, MG, MK, MN, MW, MX, MZ, NA, NI, NO, NZ, OM, PG, PH, PL, PT, RO, RU, SC, SD, SE, SG, SK, SL, SY, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, YU, ZA, ZM, ZW; RW: AT, BE, BF, BJ, CF, CG, CH, CI, CM, CY, DE, DK, ES, FI, FR, GA, GB, GR, IE, IT, LU, MC, ML, MR, NE, NL, PT, SE, SN, TD, TG, TR. (English). (World Intellectual Property Organization). CODEN: PIXXD2. CLASS: ICM: A01N047-36. ICS: A01N025-30. APPLICATION: WO 2004-JP9598 30 Jun 2004. PRIORITY: JP 2003-280259 25 Jul 2003. DOCUMENT TYPE: Patent CA Section: 5 (Agrochemical Bioregulators) The herbicidal effect of a sulfonylurea compd. or its salt is enhanced markedly by an alkoxylated glyceride. Thus, water-dispersible granules contg. nicosulfuron (5 g a.i./ha) was dild. with water corresponding to 300 L/ha, and an alkoxylated glyceride (Emanon CH 80) was added thereto in a concn. 90982-32-4 and 173159-57-4 which are cas registry numbers of substances are two of reagents here. of 0.025 wt.% , followed by foliar application to redroot pigweed (Amaranthus retroflexus). The alkoxylated glyceride enhanced the herbicidal effect of nicosulfuron more distinctly than the com. available adjuvant Citowett did, even at the same concn. .
Preparation of aminophenylsulfonylureidoazines
Preparation of aminophenylsulfonylureidoazines. Schnabel, Gerhard; Vermehren, Jan; Willms, Lothar (Hoechst Schering Agrevo Gmbh, Germany). Ger.In this article, certain chemicals are used. One of their cas registry numbers is 173159-57-4 Offen. 173159-57-4 are also occured in this study. DE 19540701 A1 7 May 1997, 15 pp. (German). (Germany). CODEN: GWXXBX. CLASS: ICM: C07D239-69. ICS: C07D239-52; C07D251-46; A01N047-36. ICA: C07D521-00. APPLICATION: DE 1995-19540701 2 Nov 1995. DOCUMENT TYPE: Patent CA Section: 28 (Heterocyclic Compounds (More Than One Hetero Atom)) Title compds. [I; R = halo, alkyl, alkoxy; n = 0-3; A = H, acyl; R1 = H, (substituted) hydrocarbyl, hydrocarbyloxy; R2 = H, (substituted) hydrocarbyl; NR1R2 = (substituted) heterocyclyl; R3 = H, alkyl; X, Y = halo, (substituted) alkyl, alkoxy, alkylthio; Z = CH, N], were prepd. starting from nitrobenzoic acids (II). Thus, a mixt. of NaOCN, 2-amino-4,6-dimethoxypyrimidine, and 2-dimethylaminocarbonyl-5-nitrobenzenesulfonyl chloride (prepn. given) was stirred in MeCN/pyridine to give 2-dimethylaminocarbonyl-5-nitro-N-[(4,6-dimethoxypyrimidin-2-yl)amino carbonyl]benzenesulfonamide. This in aq. NaOH was hydrogenated over Pd/C to give 2-dimethylaminocarbonyl-5-amino-N-[(4,6-dimethoxypyrimidin-2-yl)ami nocarbonyl]benzenesulfonamide. ..
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