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C29H34O3S2

Base Information Edit
  • Chemical Name:C29H34O3S2
  • CAS No.:102306-87-6
  • Molecular Formula:C29H34O3S2
  • Molecular Weight:494.719
  • Hs Code.:
  • Mol file:102306-87-6.mol
C<sub>29</sub>H<sub>34</sub>O<sub>3</sub>S<sub>2</sub>

Synonyms:C29H34O3S2

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Chemical Property of C29H34O3S2 Edit
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Technology Process of C29H34O3S2

There total 17 articles about C29H34O3S2 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:
Multi-step reaction with 17 steps
1: (COCl2)2 / benzene
3: Irradiation
4: SeO2 / pyridine; dioxane
5: BF3*Et2O / CH2Cl2
6: n-BuLi / tetrahydrofuran / -78 °C
7: 1.) NaH; 2.) n-BuLi, TMEDA / 1.) THF, 0 deg C, 1 h; 2.) THF, -78 deg C to -23 deg C, 2,5 h; 3.) THF, -40 deg C
8: 4-pyrrolidinopyridine, Et3N / CH2Cl2
9: NaHB4, CeCl3
10: PPTS / CH2Cl2
11: 2N NaOH / ethanol; pyridine
12: CrO3*2Py
13: NaH / toluene / 10 h / 42 °C
14: 92 percent / NaBH4, CeCl3
15: DIAD, Ph3P / tetrahydrofuran
16: 0.2N HCl
17: CrO3*Py
With hydrogenchloride; sodium hydroxide; sodium tetrahydroborate; n-butyllithium; selenium(IV) oxide; cerium(III) chloride; N,N,N,N,-tetramethylethylenediamine; di-isopropyl azodicarboxylate; chromium trioxide-pyridine complex; (COCl2)2; boron trifluoride diethyl etherate; pyridinium p-toluenesulfonate; dipyridine chromium trioxide; sodium hydride; 4-pyrrolidin-1-ylpyridine; triethylamine; triphenylphosphine; In tetrahydrofuran; 1,4-dioxane; pyridine; ethanol; dichloromethane; toluene; benzene;
DOI:10.1021/ja00271a054
Guidance literature:
Multi-step reaction with 16 steps
2: Irradiation
3: SeO2 / pyridine; dioxane
4: BF3*Et2O / CH2Cl2
5: n-BuLi / tetrahydrofuran / -78 °C
6: 1.) NaH; 2.) n-BuLi, TMEDA / 1.) THF, 0 deg C, 1 h; 2.) THF, -78 deg C to -23 deg C, 2,5 h; 3.) THF, -40 deg C
7: 4-pyrrolidinopyridine, Et3N / CH2Cl2
8: NaHB4, CeCl3
9: PPTS / CH2Cl2
10: 2N NaOH / ethanol; pyridine
11: CrO3*2Py
12: NaH / toluene / 10 h / 42 °C
13: 92 percent / NaBH4, CeCl3
14: DIAD, Ph3P / tetrahydrofuran
15: 0.2N HCl
16: CrO3*Py
With hydrogenchloride; sodium hydroxide; sodium tetrahydroborate; n-butyllithium; selenium(IV) oxide; cerium(III) chloride; N,N,N,N,-tetramethylethylenediamine; di-isopropyl azodicarboxylate; chromium trioxide-pyridine complex; boron trifluoride diethyl etherate; pyridinium p-toluenesulfonate; dipyridine chromium trioxide; sodium hydride; 4-pyrrolidin-1-ylpyridine; triethylamine; triphenylphosphine; In tetrahydrofuran; 1,4-dioxane; pyridine; ethanol; dichloromethane; toluene;
DOI:10.1021/ja00271a054
Guidance literature:
Multi-step reaction with 14 steps
1: SeO2 / pyridine; dioxane
2: BF3*Et2O / CH2Cl2
3: n-BuLi / tetrahydrofuran / -78 °C
4: 1.) NaH; 2.) n-BuLi, TMEDA / 1.) THF, 0 deg C, 1 h; 2.) THF, -78 deg C to -23 deg C, 2,5 h; 3.) THF, -40 deg C
5: 4-pyrrolidinopyridine, Et3N / CH2Cl2
6: NaHB4, CeCl3
7: PPTS / CH2Cl2
8: 2N NaOH / ethanol; pyridine
9: CrO3*2Py
10: NaH / toluene / 10 h / 42 °C
11: 92 percent / NaBH4, CeCl3
12: DIAD, Ph3P / tetrahydrofuran
13: 0.2N HCl
14: CrO3*Py
With hydrogenchloride; sodium hydroxide; sodium tetrahydroborate; n-butyllithium; selenium(IV) oxide; cerium(III) chloride; N,N,N,N,-tetramethylethylenediamine; di-isopropyl azodicarboxylate; chromium trioxide-pyridine complex; boron trifluoride diethyl etherate; pyridinium p-toluenesulfonate; dipyridine chromium trioxide; sodium hydride; 4-pyrrolidin-1-ylpyridine; triethylamine; triphenylphosphine; In tetrahydrofuran; 1,4-dioxane; pyridine; ethanol; dichloromethane; toluene;
DOI:10.1021/ja00271a054
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