Reaction #4143349
Related Literature (1)
openreactiondata ↗doi:10.1039/C8SC04228D
Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-bc2d8376644e4f5e87654ae76014e09bNo renderable structure data available
C1=CC(=CC=C1C(=O)CBr)FChemical Intermediate
Structures, identifiers and computed properties have been matched to the database record by CAS.
| Intermediates | 2-bromo-1-(4-fluorophenyl)ethanone |
|---|---|
| IUPAC Name | — |
| CAS Number | 403-29-2 |
| Database ID | 96749 |
| Molecular Formula | — |
| Molecular Weight | — |
Product Information
2-bromo-1-(4-fluorophenyl)ethanone (CAS 403-29-2) product identity, structure identifiers and related reaction data for chemical intermediate research and sourcing review.
Potential Applications
For professional research and industrial use only
Database ID 96749
Safety Notice
For professional research and industrial use only. Review the supplier safety data sheet before handling.
Synthesis data
12 reactions · 12 references
Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-bc2d8376644e4f5e87654ae76014e09bConditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-50239245828c4b318abce769489271c5Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-db50d9c5ebfc4484add788903c4c70afNo renderable structure data available
Conditions: temp:22.01; pressure:0.00; stir:
Procedure: 4 uL mixture of each reacted solution was collected and diluted with 36 uL ACN 4 uL mixture of each reacted solution was collected and diluted with 36 uL ACN chiral resolving regent (150 mM in DCM, 40 uL) CuI with DIPEA (400 mM in ACN) 40 uL internal standard 1-phenylprop-2-yn-1-ol (4) (25 mM in ACN) 40 uL After the reaction, 10 uL of supernatant for each reaction was transferred to another 96-well plate After the reaction, 10 uL of supernatant for each reaction was transferred to another 96-well plate and diluted with 190 uL ACN before the IM-MS analysis
Source ID: ord-59fd04f952fe44ac80c9b1071ee3f1f7No renderable structure data available
Conditions: temp:22.01; pressure:0.00; stir:
Procedure: 4 uL mixture of each reacted solution was collected and diluted with 36 uL ACN 4 uL mixture of each reacted solution was collected and diluted with 36 uL ACN chiral resolving regent (150 mM in DCM, 40 uL) CuI with DIPEA (400 mM in ACN) 40 uL internal standard 1-phenylprop-2-yn-1-ol (4) (25 mM in ACN) 40 uL After the reaction, 10 uL of supernatant for each reaction was transferred to another 96-well plate After the reaction, 10 uL of supernatant for each reaction was transferred to another 96-well plate and diluted with 190 uL ACN before the IM-MS analysis
Source ID: ord-3f502e402956406bad0c2bfbeb249853No renderable structure data available
Conditions: temp:22.01; pressure:0.00; stir:
Procedure: 4 uL mixture of each reacted solution was collected and diluted with 36 uL ACN 4 uL mixture of each reacted solution was collected and diluted with 36 uL ACN chiral resolving regent (150 mM in DCM, 40 uL) CuI with DIPEA (400 mM in ACN) 40 uL internal standard 1-phenylprop-2-yn-1-ol (4) (25 mM in ACN) 40 uL After the reaction, 10 uL of supernatant for each reaction was transferred to another 96-well plate After the reaction, 10 uL of supernatant for each reaction was transferred to another 96-well plate and diluted with 190 uL ACN before the IM-MS analysis
Source ID: ord-3a9d31b03d754b539ee384fc6732addbNo renderable structure data available
Conditions: temp:22.01; pressure:0.00; stir:
Procedure: 4 uL mixture of each reacted solution was collected and diluted with 36 uL ACN 4 uL mixture of each reacted solution was collected and diluted with 36 uL ACN chiral resolving regent (150 mM in DCM, 40 uL) CuI with DIPEA (400 mM in ACN) 40 uL internal standard 1-phenylprop-2-yn-1-ol (4) (25 mM in ACN) 40 uL After the reaction, 10 uL of supernatant for each reaction was transferred to another 96-well plate After the reaction, 10 uL of supernatant for each reaction was transferred to another 96-well plate and diluted with 190 uL ACN before the IM-MS analysis
Source ID: ord-1d4d472a19cd48e6a371ac27916d2a3bNo renderable structure data available
Conditions: temp:22.01; pressure:0.00; stir:
Procedure: 4 uL mixture of each reacted solution was collected and diluted with 36 uL ACN 4 uL mixture of each reacted solution was collected and diluted with 36 uL ACN chiral resolving regent (150 mM in DCM, 40 uL) CuI with DIPEA (400 mM in ACN) 40 uL internal standard 1-phenylprop-2-yn-1-ol (4) (25 mM in ACN) 40 uL After the reaction, 10 uL of supernatant for each reaction was transferred to another 96-well plate After the reaction, 10 uL of supernatant for each reaction was transferred to another 96-well plate and diluted with 190 uL ACN before the IM-MS analysis
Source ID: ord-2705d01b26eb44f68eb0b3f8145aead6No renderable structure data available
Conditions: temp:22.01; pressure:0.00; stir:
Procedure: 4 uL mixture of each reacted solution was collected and diluted with 36 uL ACN 4 uL mixture of each reacted solution was collected and diluted with 36 uL ACN chiral resolving regent (150 mM in DCM, 40 uL) CuI with DIPEA (400 mM in ACN) 40 uL internal standard 1-phenylprop-2-yn-1-ol (4) (25 mM in ACN) 40 uL After the reaction, 10 uL of supernatant for each reaction was transferred to another 96-well plate After the reaction, 10 uL of supernatant for each reaction was transferred to another 96-well plate and diluted with 190 uL ACN before the IM-MS analysis
Source ID: ord-bf16d286caf54246995e3216a039942cNo renderable structure data available
Conditions: temp:22.01; pressure:0.00; stir:
Procedure: 4 uL mixture of each reacted solution was collected and diluted with 36 uL ACN 4 uL mixture of each reacted solution was collected and diluted with 36 uL ACN chiral resolving regent (150 mM in DCM, 40 uL) CuI with DIPEA (400 mM in ACN) 40 uL internal standard 1-phenylprop-2-yn-1-ol (4) (25 mM in ACN) 40 uL After the reaction, 10 uL of supernatant for each reaction was transferred to another 96-well plate After the reaction, 10 uL of supernatant for each reaction was transferred to another 96-well plate and diluted with 190 uL ACN before the IM-MS analysis
Source ID: ord-8fc4def655514dd08454f95558a39962No renderable structure data available
Conditions: temp:22.01; pressure:0.00; stir:
Procedure: 4 uL mixture of each reacted solution was collected and diluted with 36 uL ACN 4 uL mixture of each reacted solution was collected and diluted with 36 uL ACN chiral resolving regent (150 mM in DCM, 40 uL) CuI with DIPEA (400 mM in ACN) 40 uL internal standard 1-phenylprop-2-yn-1-ol (4) (25 mM in ACN) 40 uL After the reaction, 10 uL of supernatant for each reaction was transferred to another 96-well plate After the reaction, 10 uL of supernatant for each reaction was transferred to another 96-well plate and diluted with 190 uL ACN before the IM-MS analysis
Source ID: ord-4dadfeb433e44ffe8a660abe8870bd3cNo renderable structure data available
Conditions: temp:22.01; pressure:0.00; stir:
Procedure: 4 uL mixture of each reacted solution was collected and diluted with 36 uL ACN 4 uL mixture of each reacted solution was collected and diluted with 36 uL ACN chiral resolving regent (150 mM in DCM, 40 uL) CuI with DIPEA (400 mM in ACN) 40 uL internal standard 1-phenylprop-2-yn-1-ol (4) (25 mM in ACN) 40 uL After the reaction, 10 uL of supernatant for each reaction was transferred to another 96-well plate After the reaction, 10 uL of supernatant for each reaction was transferred to another 96-well plate and diluted with 190 uL ACN before the IM-MS analysis
Source ID: ord-2381f3daee3c4161868b1b1d5189b243PubChem References
These sources are listed in the compound's public database record.
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