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Detail of "1788-10-9"

  • MSDS Download
  • CAS Number:
  • 1788-10-9
  • Name:
  • Benzenesulfonylchloride, 4-acetyl-

  • Superlist Name:
  • 4-Acetylbenzenesulfonyl chloride
  • Molecular Structure:
  • Formula:
  • C8H7ClO3S
  • Molecular Weight:
  • 218.66
  • Synonyms:
  • Benzenesulfonylchloride, p-acetyl- (6CI,7CI,8CI);4-Acetylbenzene-1-sulfonyl chloride;4-Acetylphenylsulfonyl chloride;NSC 104128;p-Acetylbenzenesulfonyl chloride;
  • Density:
  • 1.387 g/cm3
  • Melting Point:
  • 84-87 °C
  • Boiling Point:
  • 338.6 °C at 760mmHg
  • Flash Point:
  • 158.6 °C
  • Appearance:
  • brown crystalline powder
  • Hazard Symbols:
  • CorrosiveC, IrritantXi
  • Risk Codes:
  • 34-36/37/38
  • Safety:
  • 26-36/37/39-45-25-36 Details
  • Transport Information:
  • UN 3261 8/PG 3

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CAS No.1788-10-9 4-Acetylbenzenesulfonyl chloride

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CAS No.1788-10-9 4-Acetylbenzenesulfonyl chloride

4-Acetylbenzenesulfonyl chloride

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CAS No.1788-10-9 4-Acetylbenzenesulfonyl chloride

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CAS No.1788-10-9 4-Acetylbenzenesulfonyl chloride

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CAS No.1788-10-9 4-Acetylbenzenesulfonyl chloride

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CAS No.1788-10-9 4-Acetylbenzenesulfonyl chloride

Assay:98%  Appearance:White powder  Package:According to...

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

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CAS No.1788-10-9 4-Acetylbenzenesulfonyl chloride

4-Acetylbenzenesulfonyl Chloride

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CAS No.1788-10-9 4-Acetylbenzenesulfonyl chloride

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CAS No.1788-10-9 4-Acetylbenzenesulfonyl chloride

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CAS No.1788-10-9 4-Acetylbenzenesulfonyl chloride

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CAS No.1788-10-9 4-Acetylbenzenesulfonyl chloride

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Reference

Preparation of (4-pyridinylmethyl)sulfonamide derivatives as fungicidal plant protection agents
Some chemicals with cas registry numbers like 1788-10-9 are also used. Preparation of (4-pyridinylmethyl)sulfonamide derivatives as fungicidal plant protection agents. Grammenos, Wassilios; Blettner, Carsten; Mueller, Bernd; Gewehr, Markus; Tormo i Blasco, Jordi; Grote, Thomas; Rheinheimer, Joachim; Schaefer, Peter; Schieweck, Frank; Schwoegler, Anja; Wagner, Oliver; Goetz, Norbert; Strathmann, Siegfried; Schoefl, Ulrich; Scherer, Maria; Stierl, Reinhard (BASF Aktiengesellschaft, Germany). PCT Int. Appl. WO 2005033081 A1 14 Apr 2005, 40 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, JP, 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. (German). (World Intellectual Property Organization). CODEN: PIXXD2. CLASS: ICM: C07D213-42. APPLICATION: WO 2004-EP10124 10 Sep 2004. PRIORITY: EP 2003-21098 18 Sep 2003. DOCUMENT TYPE: Patent CA Section: 27 (Heterocyclic Compounds (One Hetero Atom)) Section cross-reference(s): 5, 10 The invention relates to sulfonamides I [R1 = H, alkyl, alkoxy, alkenyl, alkynyl; R2, R3, R4, R5 = hydrogen, halogen, alkyl, alkoxy or halomethyl; R2R3 = Ph, cyclopentyl, or cyclohexyl ring (whereby said ring can optionally be substituted with R2' and R3'); R2', R3' = H, halogen, alkyl, alkoxy or halomethyl; in the case (a), when R2, R3, R4 and R5 = H, X = Ph, substituted with a group -C(R6):NOR7; R6 = alkyl; R7 = alkyl, benzyl, alkenyl, haloalkyl, haloalkenyl, alkynyl, haloalkynyl; in case (b), when at least one of the groups R2, R3, R4 and R5 1 H, X = Ph, naphthyl or a five- or six-membered satd., partially unsatd., or arom. heterocycle, bonded by means of a C atom, comprising one to four heteroatoms from the group O, N or S, where X can be substituted as per the description]. The prepn. of I comprises reaction of 4-picolylamine II with sulfonic acid chlorides, XSO2Cl under basic conditions. Thus, N-methyl-N-[(4-pyridinyl)methyl]-4-[1-(ethoxyimino)ethyl]-benzenesulfona mide [I; R1 = Me, R2 = R3 = R4 = R5 = H, X = C6H4(CMe:NOEt)-4] was prepd. from 4-picolylamine via sulfonylation with 4-MeCOC6H4SO2Cl in Et2O contg. catalytic pyridine, imination with aq. EtONH2 in MeOH, and N-methylation with MeI in DMF contg. NaH. The invention further relates to methods for prodn. of said compds., agents comprising the same and use thereof for the control of fungal pests which are pathogenic to plants. The plant protection activity of I was detd. (70% phytoprotective effect vs. Alternaria solani and Sphaerotheca fuliginea). .
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