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Chemical Structure| 52240-28-5 Chemical Structure| 52240-28-5

Structure of 52240-28-5

Chemical Structure| 52240-28-5

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Product Details of [ 52240-28-5 ]

CAS No. :52240-28-5
Formula : C8H7BrO3S
M.W : 263.11
SMILES Code : O=C(O)CCC(C1=CC=C(Br)S1)=O
MDL No. :MFCD08276248
InChI Key :FOUVWVYUMOWJPZ-UHFFFAOYSA-N
Pubchem ID :11184604

Safety of [ 52240-28-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 52240-28-5 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Upstream synthesis route of [ 52240-28-5 ]

[ 52240-28-5 ] Synthesis Path-Upstream   1~5

  • 1
  • [ 1003-09-4 ]
  • [ 108-30-5 ]
  • [ 52240-28-5 ]
References: [1] Journal of Organic Chemistry, 2001, vol. 66, # 22, p. 7283 - 7286.
[2] Organic Syntheses, 2002, vol. 79, p. 204 - 204.
[3] Journal of the Chemical Society, 1954, p. 4162,4165.
[4] Recueil des Travaux Chimiques des Pays-Bas, 1950, vol. 69, p. 1083,1103.
[5] Nippon Kagaku Zasshi, 1957, vol. 78, p. 779,783[6] Chem.Abstr., 1960, p. 22559.
  • 2
  • [ 1003-09-4 ]
  • [ 108-30-5 ]
  • [ 80885-88-7 ]
  • [ 52240-28-5 ]
References: [1] Patent: US4299769, 1981, A, .
  • 3
  • [ 1003-09-4 ]
  • [ 543-20-4 ]
  • [ 52240-28-5 ]
  • [ 1289489-53-7 ]
  • [ 1289489-58-2 ]
References: [1] Chemistry of Heterocyclic Compounds, 2011, vol. 46, # 10, p. 1199 - 1207.
  • 4
  • [ 1003-09-4 ]
  • [ 543-20-4 ]
  • [ 52240-28-5 ]
  • [ 1289489-53-7 ]
References: [1] Chemistry of Heterocyclic Compounds, 2011, vol. 46, # 10, p. 1199 - 1207.
  • 5
  • [ 1003-09-4 ]
  • [ 543-20-4 ]
  • [ 52240-28-5 ]
  • [ 144153-56-0 ]
  • [ 1289489-53-7 ]
References: [1] Chemistry of Heterocyclic Compounds, 2011, vol. 46, # 10, p. 1199 - 1207.
 

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• Alkyl Halide Occurrence • Arndt-Eistert Homologation • Baeyer-Villiger Oxidation • Barbier Coupling Reaction • Baylis-Hillman Reaction • Bucherer-Bergs Reaction • Clemmensen Reduction • Corey-Bakshi-Shibata (CBS) Reduction • Corey-Chaykovsky Reaction • Fischer Indole Synthesis • General Reactivity • Grignard Reaction • Henry Nitroaldol Reaction • Hiyama Cross-Coupling Reaction • Horner-Wadsworth-Emmons Reaction • Hunsdiecker-Borodin Reaction • Hydride Reductions • Kinetics of Alkyl Halides • Kumada Cross-Coupling Reaction • Lawesson's Reagent • Leuckart-Wallach Reaction • McMurry Coupling • Meerwein-Ponndorf-Verley Reduction • Passerini Reaction • Paternò-Büchi Reaction • Petasis Reaction • Peterson Olefination • Pictet-Spengler Tetrahydroisoquinoline Synthesis • Preparation of Aldehydes and Ketones • Preparation of Amines • Preparation of Carboxylic Acids • Prins Reaction • Reactions of Aldehydes and Ketones • Reactions of Alkyl Halides with Reducing Metals • Reactions of Amines • Reactions of Carboxylic Acids • Reactions of Dihalides • Reformatsky Reaction • Robinson Annulation • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Specialized Acylation Reagents-Ketenes • Stille Coupling • Stobbe Condensation • Substitution and Elimination Reactions of Alkyl Halides • Suzuki Coupling • Tebbe Olefination • Ugi Reaction • Wittig Reaction • Wolff-Kishner Reduction

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