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C15H19IO3

Base Information
  • Chemical Name:C15H19IO3
  • CAS No.:1027982-33-7
  • Molecular Formula:C15H19IO3
  • Molecular Weight:374.219
  • Hs Code.:
C<sub>15</sub>H<sub>19</sub>IO<sub>3</sub>

Synonyms:C15H19IO3

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Chemical Property of C15H19IO3
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Technology Process of C15H19IO3

There total 1 articles about C15H19IO3 which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With triethylamine; In tetrahydrofuran; at 0 ℃; for 1h;
DOI:10.1021/jm960465t
Guidance literature:
Multi-step reaction with 6 steps
1: 1.) n-BuLi / 1.) THF, hexane, -78 deg C, 1 h, 2.) THF, hexane, from 0 deg C to RT, overnight
2: 1.) TiCl4, Ti(O-iPr)4, i-Pr2NEt / 1.) CH2Cl2, 0 deg C, 90 min, 2.) CH2Cl2, 0 deg C, overnight
3: 1.) aq. LiOH, H2O2, 2.) sodium sulfite, aq. NaHCO3 / 1.) THF, 0 deg C, 3 h, 2.) THF, 2 h
4: 1.) 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone / 1.) THF, -78 deg C, 1 h, 2.) THF, 0 deg C, overnight
5: 300 mg / EDC, DMAP / tetrahydrofuran / Ambient temperature
6: 64 percent / n-Bu4NCl, KOAc, Pd(OAc)2 / Ambient temperature
With titanium(IV) isopropylate; dmap; 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; palladium diacetate; lithium hydroxide; n-butyllithium; tetrabutyl-ammonium chloride; dihydrogen peroxide; potassium acetate; titanium tetrachloride; sodium hydrogencarbonate; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; N-ethyl-N,N-diisopropylamine; sodium sulfite; In tetrahydrofuran;
DOI:10.1021/jm960465t
Guidance literature:
Multi-step reaction with 8 steps
1: 1.) n-BuLi / 1.) THF, hexane, -78 deg C, 1 h, 2.) THF, hexane, from 0 deg C to RT, overnight
2: 1.) TiCl4, Ti(O-iPr)4, i-Pr2NEt / 1.) CH2Cl2, 0 deg C, 90 min, 2.) CH2Cl2, 0 deg C, overnight
3: 1.) aq. LiOH, H2O2, 2.) sodium sulfite, aq. NaHCO3 / 1.) THF, 0 deg C, 3 h, 2.) THF, 2 h
4: 1.) 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone / 1.) THF, -78 deg C, 1 h, 2.) THF, 0 deg C, overnight
5: 300 mg / EDC, DMAP / tetrahydrofuran / Ambient temperature
6: 240 mg / aq. Na2CO3, KBr, Pd(PPh3)4 / toluene; ethanol / 6 h / 95 °C
7: 190 mg / Bu4NF / dimethylformamide; tetrahydrofuran / 4 h / Ambient temperature
8: 135 mg / HOBt, EDC, N-methylmorpholine / tetrahydrofuran / Ambient temperature
With 4-methyl-morpholine; titanium(IV) isopropylate; dmap; 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; lithium hydroxide; tetrakis(triphenylphosphine) palladium(0); n-butyllithium; tetrabutyl ammonium fluoride; dihydrogen peroxide; titanium tetrachloride; sodium hydrogencarbonate; sodium carbonate; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; N-ethyl-N,N-diisopropylamine; potassium bromide; sodium sulfite; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide; toluene;
DOI:10.1021/jm960465t
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