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Detail of > 1113-59-3

  • MSDS Download
  • CAS Number:
  • 1113-59-3
  • Name:
  • Propanoic acid,3-bromo-2-oxo-

  • Superlist Name:
  • Bromopyruvic acid
  • Formula:
  • C3H3BrO3
  • Molecular Structure:
  • Synonyms:
  • Pyruvicacid, bromo- (6CI,7CI,8CI);3-Bromo-2-oxopropanoic acid;3-Bromopyruvate;3-Bromopyruvic acid;NSC 11731;NSC 62343;b-Bromopyruvic acid;
  • Molecular Weight:
  • 166.96
  • EINECS:
  • 214-206-5
  • Density:
  • 2.011 g/cm3
  • Melting Point:
  • 77-82 °C
  • Boiling Point:
  • 223.4 °C at 760 mmHg
  • Flash Point:
  • 88.9 °C
  • Hazard Symbols:
  • CorrosiveC
  • Risk Codes:
  • 34-20/21/22
  • Safety:
  • 26-36/37/39-45-27Details
  • Transport Information:
  • UN 3261 8/PG 2
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1113-59-3 Bromopyruvic acid

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1113-59-3 Bromopyruvic acid

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1113-59-3 Bromopyruvic acid

Chemical Name: Bromopyruvic acid Molecular Formula: C3H3BrO3 Formula Weight: 166.96 CAS No.: 1113-59-3 MOL File: Mol file
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1113-59-3 Bromopyruvic acid

Product name:3-Bromopyruvic Acid Hydrate Appearance:white to light yellow powder Content:97%(By Titration NaOH 0.1N)
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1113-59-3 Bromopyruvic acid

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3-BROMOPYRUVIC ACID
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    Reference

    Cis-1,2-Diaminocyclohexane platinum complexes
    Cis-1,2-Diaminocyclohexane platinum complexes. (Fabrica de Productos Quimicos y Farmaceuticos Abello S. A., Spain). Belg. BE 898614 A1 2 May 1984, 16 pp. (French). (Belgium). CODEN: BEXXAL. ICI: A61. APPLICATION: BE 21-161 5 Jan 1984. DOCUMENT TYPE: Patent CA Section: 63 (Pharmaceuticals) Section cross-reference(s): 1, 49 cis-1,2-Diaminocyclohexane platinum (II) complexes (I, X and Y = sulfates, sulfonates, nitrates, carboxylates, etc.) are prepd. for use as neoplasm inhibitors. Cis-dichloro-1,2-diaminocyclohexane platinum [52691-24-4] was treated with AgNO3 and the resulting dinitrate complex [81473-15-6] obtained was further treated with 3-bromopyruvic acid [1113-59-3] to yield cis-bis(3-bromopyruvato)-1,2-diaminocyclohexaneplatinum [92389-55-4]. The yield was 70%.
    Enzymic production of aminoethylcysteine ketimine
    Enzymic production of aminoethylcysteine ketimine. Chiaraluce, Roberta; Nardini, Mirella; Dupre, Silvestro; Ricci, Giorgio; Cavallini, Doriano (Inst. Biol. Chem., Univ. Roma "La Sapienza", Rome, Italy). IRCS Med. Sci.: Libr. Compend. 1113-59-3 and 89648-14-6 are cas registry numbers of chemicals which are used as reagents here., 11(12), 1119-20 (English) 1983. CODEN: IRLCDZ. ISSN: 0305-6651. DOCUMENT TYPE: Journal CA Section: 7 (Enzymes) Section cross-reference(s): 6 Aminoethylcysteine ketimine (I) was produced on incubation of pantetheine or S-pyruvoyl pantetheine with horse kidney homogenate. The I-forming activity copurified from the homogenate with cysteamine-forming activity. The enzyme responsible for I formation in the horse kidney apparently is pantetheinase. .

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