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Chemical Structure| 105694-44-8 Chemical Structure| 105694-44-8

Structure of 105694-44-8

Chemical Structure| 105694-44-8

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Product Details of [ 105694-44-8 ]

CAS No. :105694-44-8
Formula : C8H5BrO2
M.W : 213.03
SMILES Code : O=C1OCC2=C1C(Br)=CC=C2
MDL No. :MFCD18204744
Boiling Point : No data available
InChI Key :BSKYWJYGAQMPLU-UHFFFAOYSA-N
Pubchem ID :13720121

Safety of [ 105694-44-8 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H312-H332
Precautionary Statements:P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P330-P362-P403+P233-P501

Application In Synthesis of [ 105694-44-8 ]

* 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 [ 105694-44-8 ]

[ 105694-44-8 ] Synthesis Path-Upstream   1~2

  • 1
  • [ 82-73-5 ]
  • [ 102308-43-0 ]
  • [ 105694-44-8 ]
References: [1] Canadian Journal of Chemistry, 1987, vol. 65, p. 1214 - 1217.
[2] Journal of Organic Chemistry, 1987, vol. 52, # 1, p. 129 - 134.
[3] Journal of Organic Chemistry, 1987, vol. 52, # 1, p. 129 - 134.
  • 2
  • [ 82-73-5 ]
  • [ 102308-43-0 ]
  • [ 105694-44-8 ]
References: [1] Journal of Organic Chemistry, 1987, vol. 52, # 1, p. 129 - 134.
 

Historical Records

Technical Information

• Acyl Group Substitution • Alkyl Halide Occurrence • Baeyer-Villiger Oxidation • Barbier Coupling Reaction • Baylis-Hillman Reaction • Bouveault-Blanc Reduction • Bucherer-Bergs Reaction • Catalytic Hydrogenation • Clemmensen Reduction • Complex Metal Hydride Reductions • Corey-Bakshi-Shibata (CBS) Reduction • Corey-Chaykovsky Reaction • Ester Cleavage • Fischer Indole Synthesis • General Reactivity • Grignard Reaction • Henry Nitroaldol Reaction • Hiyama Cross-Coupling Reaction • Horner-Wadsworth-Emmons 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 • Prins Reaction • Reactions of Aldehydes and Ketones • Reactions of Alkyl Halides with Reducing Metals • Reactions of Amines • Reactions of Dihalides • Reactions with Organometallic Reagents • Reformatsky Reaction • Robinson Annulation • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Specialized Acylation Reagents-Carbodiimides and Related Reagents • 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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