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Chemical Structure| 1889-26-5 Chemical Structure| 1889-26-5

Structure of Valeryl Bromide
CAS No.: 1889-26-5

Chemical Structure| 1889-26-5

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Synonyms: Valeroyl Bromide

4.5 *For Research Use Only! Not for Human Use. We Do Not Sell to Patients.

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Product Details of [ 1889-26-5 ]

CAS No. :1889-26-5
Formula : C5H9BrO
M.W : 165.03
SMILES Code : CCCCC(Br)=O
Synonyms :
Valeroyl Bromide
English Name :Pentanoyl bromide
MDL No. :MFCD00059467
InChI Key :FDOHPUYPQQKECS-UHFFFAOYSA-N
Pubchem ID :11137484

Safety of [ 1889-26-5 ]

Application In Synthesis of [ 1889-26-5 ]

* 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 [ 1889-26-5 ]

[ 1889-26-5 ] Synthesis Path-Downstream   1~14

  • 1
  • [ 1889-26-5 ]
  • [ 147776-56-5 ]
  • [ 147776-45-2 ]
YieldReaction ConditionsOperation in experiment
With sodium hydride 1.) DMF, RT, 3 h, 2.) DMF, 50 deg C, overnight; Yield given. Multistep reaction;
  • 2
  • [ 1889-26-5 ]
  • [ CAS Unavailable ]
  • [ 1027955-16-3 ]
YieldReaction ConditionsOperation in experiment
With sodium hydride 1.) DMF, RT, 3 h, 2.) DMF, 50 deg C, overnight; Yield given. Multistep reaction;
  • 3
  • [ 1889-26-5 ]
  • [ 147776-38-3 ]
  • [ 147776-40-7 ]
YieldReaction ConditionsOperation in experiment
With sodium hydride 1.) DMF, RT, 3 h, 2.) DMF, 50 deg C, overnight; Yield given. Multistep reaction;
  • 4
  • [ 1889-26-5 ]
  • [ 19790-60-4 ]
  • [ 652150-96-4 ]
  • [ CAS Unavailable ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
With (S,S)-ArSO2NCH(i-Pr)CH2N(CH2CF3)CH2CH(i-Pr)NSO2CF3*AlMe; N-ethyl-N,N-diisopropylamine In various solvent(s) at -25℃; for 14h; Title compound not separated from byproducts;
  • 5
  • [ 1889-26-5 ]
  • [ 100-52-7 ]
  • [ 652150-97-5 ]
YieldReaction ConditionsOperation in experiment
85% With (S,S)-ArSO2NCH(i-Pr)CH2N(CH2CF3)CH2CH(i-Pr)NSO2CF3*AlMe; N-ethyl-N,N-diisopropylamine In various solvent(s) at -25℃; for 14h;
  • 6
  • [ 1889-26-5 ]
  • [ 544-92-3 ]
  • [ 38576-59-9 ]
YieldReaction ConditionsOperation in experiment
75% at 90℃; for 2h;
  • 7
  • [ 1889-26-5 ]
  • [ 952314-24-8 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: 75 percent / 2 h / 90 °C 2: Et3N / {(1R,2R)-[(3,5-tBu2-2-OH-C6H2)-(E)-CH=N]2-cyclohexane-TiO3}2 / CH2Cl2 / 10 h / -40 °C
  • 8
  • [ 1889-26-5 ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: 75 percent / 2 h / 90 °C 2: Et3N / {(1R,2R)-[(3,5-tBu2-2-OH-C6H2)-(E)-CH=N]2-cyclohexane-TiO3}2 / CH2Cl2 / 10 h / -40 °C
  • 9
  • [ 1889-26-5 ]
  • [ 93730-06-4 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: (i) AlCl3, CS2, (ii) aq. HCl 2: KOH, aq. N2H4*H2O / ethane-1,2-diol / Heating
  • 10
  • [ 1889-26-5 ]
  • [ 95441-28-4 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: (i) AlCl3, CS2, (ii) aq. HCl 2: KOH, aq. N2H4*H2O / ethane-1,2-diol / Heating 3: (i) NaNH2, xylene, (ii) /BRN= 605300/
  • 11
  • [ 104-53-0 ]
  • [ 1889-26-5 ]
  • [ 1057557-82-0 ]
YieldReaction ConditionsOperation in experiment
91% With 2Br(1-)*C41H51AlN4O2(2+); N-ethyl-N,N-diisopropylamine In dichloromethane at -70℃; for 24h; Inert atmosphere; optical yield given as %ee;
91% With 2Br(1-)*C41H51AlN4O2(2+); N-ethyl-N,N-diisopropylamine In dichloromethane at -70℃; for 24h; Inert atmosphere; optical yield given as %ee; enantioselective reaction;
  • 12
  • [ 110-62-3 ]
  • [ 1889-26-5 ]
  • [ 1057557-98-8 ]
YieldReaction ConditionsOperation in experiment
92% With 2Br(1-)*C41H51AlN4O2(2+); N-ethyl-N,N-diisopropylamine In dichloromethane at -70℃; for 24h; Inert atmosphere; optical yield given as %ee;
92% With 2Br(1-)*C41H51AlN4O2(2+); N-ethyl-N,N-diisopropylamine In dichloromethane at -70℃; for 24h; Inert atmosphere; optical yield given as %ee; enantioselective reaction;
  • 13
  • [ 764-59-0 ]
  • [ 1889-26-5 ]
  • [ 1057557-86-4 ]
YieldReaction ConditionsOperation in experiment
96% With 2Br(1-)*C41H51AlN4O2(2+); N-ethyl-N,N-diisopropylamine In dichloromethane at -70℃; for 24h; Inert atmosphere; optical yield given as %ee;
96% With 2Br(1-)*C41H51AlN4O2(2+); N-ethyl-N,N-diisopropylamine In dichloromethane at -70℃; for 24h; Inert atmosphere; optical yield given as %ee; enantioselective reaction;
  • 14
  • [ 1889-26-5 ]
  • [ CAS Unavailable ]
  • [ 1057557-90-0 ]
YieldReaction ConditionsOperation in experiment
63% With 2Br(1-)*C41H51AlN4O2(2+); N-ethyl-N,N-diisopropylamine In dichloromethane at -70℃; for 24h; Inert atmosphere; optical yield given as %ee;
63% With 2Br(1-)*C41H51AlN4O2(2+); N-ethyl-N,N-diisopropylamine In dichloromethane at -70℃; for 24h; Inert atmosphere; optical yield given as %ee; enantioselective reaction;
 

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