Alternatived Products of [ 29558-78-9 ]
Product Details of [ 29558-78-9 ]
CAS No. : | 29558-78-9 |
MDL No. : | MFCD02258843 |
Formula : |
C12H9IO
|
Boiling Point : |
- |
Linear Structure Formula : | - |
InChI Key : | - |
M.W : |
296.10
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Pubchem ID : | - |
Synonyms : |
|
Application In Synthesis of [ 29558-78-9 ]
* 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 [ 29558-78-9 ]
- 1
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[ 1204-79-1 ]
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[ 29558-78-9 ]
- 2
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[ 7285-77-0 ]
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[ 29558-78-9 ]
Yield | Reaction Conditions | Operation in experiment |
|
Diazotization; |
|
- 3
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[ 29558-78-9 ]
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[ 61135-33-9 ]
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[ 1034147-10-8 ]
- 4
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[ 768-95-6 ]
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[ 29558-78-9 ]
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[ 1221259-68-2 ]
Yield | Reaction Conditions | Operation in experiment |
93% |
With sulfuric acid In acetic acid at 20℃; for 50h; |
64.A
To a mixture of 4'- iodobiphenyl-4-ol (0.332 g, 2 mmol) and 1 -admantanol (0.15 g, 0.51 mmol) in AcOH (2 ml) concentrated H2SO4 (0.5 ml) was added and the reaction mixture was stirred for 50 h at room temperature. This was diluted to 100 ml with EtOAc and washed with NaHCO3 solution, dried over MgSO4 and filtered. The filtrate was evaporated to dryness and the residue was crystallized from MeOH to give the product (0.195 g; 93%), as a colourless paste. 1 H NMR (CDCI3) 1.78 (m, 6H); 2.07(s, 3H); 2.15 (s, 6H); 6.69 (d, 1 H, J = 8.15 Hz); 7.21 - 7.28 (m, 3H); 7.37(d, 1 H, J = 2.28 Hz); 7.69 (d, 2H, J = 8.45 Hz). |
- 5
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[ 29558-78-9 ]
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[ 1066-54-2 ]
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[ 1202355-37-0 ]
- 6
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[ 29558-78-9 ]
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[ 154549-38-9 ]
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2'', 4'', 6''-tri(isopropyl)-1,1':4',1''-terphenyl-4-ol
[ No CAS ]