No renderable structure data available
C1=CC(=CC=C1C(=O)CBr)BrChemical Intermediate
Structures, identifiers and computed properties have been matched to the database record by CAS.
| Intermediates | 2-bromo-1-(4-bromophenyl)ethanone |
|---|---|
| IUPAC Name | — |
| CAS Number | 99-73-0 |
| Database ID | 7454 |
| Molecular Formula | — |
| Molecular Weight | — |
Product Information
2-bromo-1-(4-bromophenyl)ethanone (CAS 99-73-0) 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 7454
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-4a7d54f36c4048e889a0d4d8fbfd47e0Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-45ce36e9af924d7184219e9b7c52853bConditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-ca7eb8199fc748d08caa260d2d3c02a2Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-3425bb77b5c84a9cb403557eb14d2b4bConditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-bbe035b060474713ba08b9d7cac2e178Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-ec0f8aaf549b4b4285b2ab418e826b78No 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-20f08d4e8e5346ce86b4b63e75f43613No 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-3d2fe2459b054eb3a33606fc2042419fNo 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-a2ec87c0fb734e8a8a1ec988b37f7a9cNo 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-bc42e44a15c24388b2607dd3f9b9e6b2No 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-ecd16c433c85487fa7344a64c06ed34fNo 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-cc358881c5004ccf94a204c73debc497PubChem References
These sources are listed in the compound's public database record.
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