C₃₈H₄₅NO₇

Base Information

Chemical Name:C₃₈H₄₅NO₇
CAS No.:134733-92-9
Molecular Formula:C₃₈H₄₅NO₇
Molecular Weight:627.778
Hs Code.:

C<sub>38</sub>H<sub>45</sub>NO<sub>7</sub>

Synonyms:C₃₈H₄₅NO₇

Suppliers and Price of C₃₈H₄₅NO₇

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Chemical Property of C₃₈H₄₅NO₇

Chemical Property:

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Technology Process of C₃₈H₄₅NO₇

There total 11 articles about C₃₈H₄₅NO₇ 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:

Reference yield: 55.0%

: 134721-16-7
(2R^*,6R^*)-2,6-Bis<(2R^*)-2-acetoxy-4-(3-iodo-4-methoxyphenyl)butyl>-1-benzoylpiperidine

: 134721-15-6
(2R^*,6R^*)-2,6-Bis<(2R^*)-2-acetoxy-4-(p-methoxyphenyl)butyl>-1-benzoylpiperidine

: 134733-92-9
C₃₈H₄₅NO₇

Guidance literature:: With bis(triphenylphosphine)nickel(II) chloride; triphenylphosphine; zinc; In N,N-dimethyl-formamide; at 50 ℃; for 21h;

Reference yield:

: 4801-58-5
N-hydroxypiperidine

: 134733-92-9
C₃₈H₄₅NO₇

Guidance literature:: Multi-step reaction with 10 steps

1: 1. HgO (yellow) / 1. CH₂Cl₂, 30min, 2. CHCl₃, reflux, 24h

2: 1. m-chloroperoxybenzoic acid (MCPBA) / 1. CHCl₂, r.t., 1h; 2. CHCl₃, reflux, 40h

3: 74 percent / Zn, ethylenediaminetetraacetic acid / acetic acid; ethanol / 0.5 h / Heating

4: 31 percent / triethylamine / benzene / 8 h

5: methanolic KOH

6: 96 percent / pyridine / 4-Dimethylaminopyridine (DMAP) / 24 h

7: H₂ / 5percent Pd/C / methanol; diethyl ether / 1.5 h / 760 Torr

8: K₂CO₃ / acetone / 4 h / Heating

9: 83 percent / I₂, silver trifluoroacetate / CH₂Cl₂; CHCl₃ / 3 h / Ambient temperature

10: 55 percent / bis(triphenylphosphine)nickel dichloride, Zn, triphenylphosphine / dimethylformamide / 21 h / 50 °C

With pyridine; potassium hydroxide; bis(triphenylphosphine)nickel(II) chloride; ethylenediaminetetraacetic acid; hydrogen; iodine; silver trifluoroacetate; potassium carbonate; triethylamine; 3-chloro-benzenecarboperoxoic acid; triphenylphosphine; mercury(II) oxide; zinc; dmap; palladium on activated charcoal; In methanol; diethyl ether; ethanol; dichloromethane; chloroform; acetic acid; N,N-dimethyl-formamide; acetone; benzene;

Reference yield:

: 134721-17-8
1-(benzyloxy)-4-(but-3-en-1-yl)benzene

: 134733-92-9
C₃₈H₄₅NO₇

Guidance literature:: Multi-step reaction with 10 steps

1: 1. HgO (yellow) / 1. CH₂Cl₂, 30min, 2. CHCl₃, reflux, 24h

2: 1. m-chloroperoxybenzoic acid (MCPBA) / 1. CHCl₂, r.t., 1h; 2. CHCl₃, reflux, 40h

3: 74 percent / Zn, ethylenediaminetetraacetic acid / acetic acid; ethanol / 0.5 h / Heating

4: 31 percent / triethylamine / benzene / 8 h

5: methanolic KOH

6: 96 percent / pyridine / 4-Dimethylaminopyridine (DMAP) / 24 h

7: H₂ / 5percent Pd/C / methanol; diethyl ether / 1.5 h / 760 Torr

8: K₂CO₃ / acetone / 4 h / Heating

9: 83 percent / I₂, silver trifluoroacetate / CH₂Cl₂; CHCl₃ / 3 h / Ambient temperature

10: 55 percent / bis(triphenylphosphine)nickel dichloride, Zn, triphenylphosphine / dimethylformamide / 21 h / 50 °C

With pyridine; potassium hydroxide; bis(triphenylphosphine)nickel(II) chloride; ethylenediaminetetraacetic acid; hydrogen; iodine; silver trifluoroacetate; potassium carbonate; triethylamine; 3-chloro-benzenecarboperoxoic acid; triphenylphosphine; mercury(II) oxide; zinc; dmap; palladium on activated charcoal; In methanol; diethyl ether; ethanol; dichloromethane; chloroform; acetic acid; N,N-dimethyl-formamide; acetone; benzene;