C₃₅H₅₂O₅

Base Information

Chemical Name:C₃₅H₅₂O₅
CAS No.:113655-42-8
Molecular Formula:C₃₅H₅₂O₅
Molecular Weight:552.795
Hs Code.:

C<sub>35</sub>H<sub>52</sub>O<sub>5</sub>

Synonyms:

Suppliers and Price of C₃₅H₅₂O₅

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of C₃₅H₅₂O₅

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
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Technology Process of C₃₅H₅₂O₅

There total 24 articles about C₃₅H₅₂O₅ 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:

: 110-87-2
3,4-dihydro-2H-pyran

: 113655-42-8
(1S*,5S*,6S*,7R*)-3-<2-(benzyloxy)ethyl>-7-(tetrahydropyran-2-yl)oxy-6-<3(S*)-(tetrahydropyran-2-yl)oxyoct-1(E)-enyl>bicyclo<3.2.1>oct-2-ene

Guidance literature:: Multi-step reaction with 6 steps

1: 839 mg / p-TsOH / CH₂Cl₂ / 0.5 h

2: 723 percent / LiAlH₄ / tetrahydrofuran / 0.5 h

3: 691 mg / sulfur trioxide/pyridine, Et₃N / dimethylsulfoxide / 0.5 h / Ambient temperature

4: 850 mg / diethyl ether / 2.5 h / Ambient temperature

5: 420 mg / NaBH₄/CeCl₃*7H₂O / methanol / 0.5 h

6: 410 mg / p-TsOH / CH₂Cl₂

With pyridine; sodium tetrahydroborate; lithium aluminium tetrahydride; cerium(III) chloride; sulfur trioxide; triethylamine; toluene-4-sulfonic acid; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; dimethyl sulfoxide;
DOI:10.1248/cpb.35.2286

Reference yield:

: 110-87-2
3,4-dihydro-2H-pyran

: 113655-42-8
C₃₅H₅₂O₅

Guidance literature:: Multi-step reaction with 6 steps

1: 839 mg / p-TsOH / CH₂Cl₂ / 0.5 h

2: 723 percent / LiAlH₄ / tetrahydrofuran / 0.5 h

3: 691 mg / sulfur trioxide/pyridine, Et₃N / dimethylsulfoxide / 0.5 h / Ambient temperature

4: 850 mg / diethyl ether / 2.5 h / Ambient temperature

5: 376 mg / NaBH₄/CeCl₃*7H₂O / methanol / 0.5 h

6: p-TsOH / CH₂Cl₂

With pyridine; sodium tetrahydroborate; lithium aluminium tetrahydride; cerium(III) chloride; sulfur trioxide; triethylamine; toluene-4-sulfonic acid; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; dimethyl sulfoxide;
DOI:10.1248/cpb.35.2286

Reference yield:

: 113639-74-0
(1S*,5S*,6R*,7R*)-3-<2-(benzyloxy)ethyl>-6-ethoxycarbonyl-7-hydroxybicyclo<3.2.1>oct-2-ene

: 113655-42-8
(1S*,5S*,6S*,7R*)-3-<2-(benzyloxy)ethyl>-7-(tetrahydropyran-2-yl)oxy-6-<3(S*)-(tetrahydropyran-2-yl)oxyoct-1(E)-enyl>bicyclo<3.2.1>oct-2-ene

Guidance literature:: Multi-step reaction with 6 steps

1: 839 mg / p-TsOH / CH₂Cl₂ / 0.5 h

2: 723 percent / LiAlH₄ / tetrahydrofuran / 0.5 h

3: 691 mg / sulfur trioxide/pyridine, Et₃N / dimethylsulfoxide / 0.5 h / Ambient temperature

4: 850 mg / diethyl ether / 2.5 h / Ambient temperature

5: 420 mg / NaBH₄/CeCl₃*7H₂O / methanol / 0.5 h

6: 410 mg / p-TsOH / CH₂Cl₂

With pyridine; sodium tetrahydroborate; lithium aluminium tetrahydride; cerium(III) chloride; sulfur trioxide; triethylamine; toluene-4-sulfonic acid; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; dimethyl sulfoxide;
DOI:10.1248/cpb.35.2286