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Chemical Structure| 112299-62-4 Chemical Structure| 112299-62-4

Structure of 112299-62-4

Chemical Structure| 112299-62-4

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Product Details of [ 112299-62-4 ]

CAS No. :112299-62-4
Formula : C8H8Br2
M.W : 263.96
SMILES Code : CC1=C(Br)C=CC=C1CBr
MDL No. :MFCD11847532
InChI Key :XVLACHXVYBTTPW-UHFFFAOYSA-N
Pubchem ID :22672648

Safety of [ 112299-62-4 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H302-H314
Precautionary Statements:P280-P305+P351+P338-P310
Class:8
UN#:1759
Packing Group:

Application In Synthesis of [ 112299-62-4 ]

* 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.

  • Downstream synthetic route of [ 112299-62-4 ]

[ 112299-62-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 773837-37-9 ]
  • [ 112299-62-4 ]
  • [ 76574-42-0 ]
YieldReaction ConditionsOperation in experiment
28.2% In N,N-dimethyl-formamide; at 100℃; for 12h; To a solution of bromo-3-bromomethyl-2-methyl-benzene (0.2 g, 7.6 mmol) in DMF (15 mL) is added sodium cyanide (0.55 g, 11.4 mmol) at room temperature. The reaction mixture is heated at 100 C for 12 hours and quenched with potassium permanganate solution, filtered, and the filtrate is diluted with water and extracted with EtOAc (2x20 mL). The organic extracts are dried over Na2SO4, filtered, and evaporated. The crude material is purified over silica gel column chromatography (combiflash),eluting with EtOAc 10-25% in hexanes to give the title compound (0.8 g, 28.2%). LCMS m/z 211 [M+Hjt
28.2% In N,N-dimethyl-formamide; at 20 - 100℃; for 12h; To a solution of bromo-3-bromomethyl-2-methyl-benzene (0.2 g, 7 6 mmol) in DMF (15 mL) is added sodium cyanide (0.55 g, 11.4 mmol) at room temperature. The reaction mixture is heated at 100 C. for 12 hours and quenched with potassium permanganate solution, filtered, and the filtrate is diluted with water and extracted with EtOAc (2*20 mL). The organic extracts are dried over Na2SO4, filtered, and evaporated. The crude material is purified over silica gel column chromatography (combiflash), eluting with EtOAc 10-25% in hexanes to give the title compound (0.8 g, 28.2%). LC-MS m/z 211 [M+H]+.
 

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