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Chemical Structure| 22190-38-1 Chemical Structure| 22190-38-1

Structure of 22190-38-1

Chemical Structure| 22190-38-1

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Product Details of [ 22190-38-1 ]

CAS No. :22190-38-1
Formula : C10H10BrNO
M.W : 240.10
SMILES Code : CC(N1CCC2=C1C=CC(Br)=C2)=O
MDL No. :MFCD00056017
InChI Key :WQKQAIXOTCPWFE-UHFFFAOYSA-N
Pubchem ID :721847

Safety of [ 22190-38-1 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H317-H319
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 22190-38-1 ]

* 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 [ 22190-38-1 ]

[ 22190-38-1 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 22190-38-1 ]
  • [ 873055-33-5 ]
References: [1] Patent: US2011/98311, 2011, A1, .
[2] Patent: US2012/309758, 2012, A1, .
[3] Patent: US2015/231142, 2015, A1, .
 

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Technical Information

• Acyl Group Substitution • Alkyl Halide Occurrence • Baeyer-Villiger Oxidation • Barbier Coupling Reaction • Baylis-Hillman Reaction • Bucherer-Bergs Reaction • Chan-Lam Coupling Reaction • Clemmensen Reduction • Complex Metal Hydride Reductions • 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 • 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 • 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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