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C19H25ClHgO5

Base Information Edit
  • Chemical Name:C19H25ClHgO5
  • CAS No.:909576-50-7
  • Molecular Formula:C19H25ClHgO5
  • Molecular Weight:569.447
  • Hs Code.:
  • Mol file:909576-50-7.mol
C<sub>19</sub>H<sub>25</sub>ClHgO<sub>5</sub>

Synonyms:C19H25ClHgO5

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Chemical Property of C19H25ClHgO5 Edit
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Technology Process of C19H25ClHgO5

There total 1 articles about C19H25ClHgO5 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 mercury(II) diacetate; In tetrahydrofuran; at 20 ℃; for 2h; diastereoselective reaction;
DOI:10.1007/s11164-012-0702-y
Guidance literature:
With sodium tetrahydroborate; oxygen; In N,N-dimethyl-formamide; at 20 ℃; for 4h;
DOI:10.1007/s11164-012-0702-y
Guidance literature:
Multi-step reaction with 9 steps
1.1: oxygen; sodium tetrahydroborate / N,N-dimethyl-formamide / 4 h / 20 °C
2.1: sodium; naphthalene / tetrahydrofuran / 0 °C
3.1: sodium hydride / 3 h / 20 °C
4.1: sodium hydride; carbon disulfide; methyl iodide / tetrahydrofuran / 2 h / 0 °C
4.2: 3 h / 90 °C
5.1: toluene-4-sulfonic acid / tetrahydrofuran; water / 2 h / 60 °C
5.2: 10 h / 0 - 20 °C
6.1: tetrahydrofuran / 10 h / 0 - 20 °C
7.1: dmap / dichloromethane / 2 h / 20 °C
8.1: mercury(II) diacetate / tetrahydrofuran / 2 h / 20 °C
9.1: oxygen; sodium tetrahydroborate / N,N-dimethyl-formamide / 4 h / 20 °C
With carbon disulfide; dmap; sodium tetrahydroborate; naphthalene; mercury(II) diacetate; oxygen; sodium; sodium hydride; toluene-4-sulfonic acid; methyl iodide; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide; 4.1: |Barton-McCombie Deoxygenation / 4.2: |Barton-McCombie Deoxygenation;
DOI:10.1007/s11164-012-0702-y
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