C₂₆H₃₆O₅S

Base Information

Chemical Name:C₂₆H₃₆O₅S
CAS No.:182625-04-3
Molecular Formula:C₂₆H₃₆O₅S
Molecular Weight:460.635
Hs Code.:

C<sub>26</sub>H<sub>36</sub>O<sub>5</sub>S

Synonyms:C₂₆H₃₆O₅S

Suppliers and Price of C₂₆H₃₆O₅S

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of C₂₆H₃₆O₅S

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₂₆H₃₆O₅S

There total 20 articles about C₂₆H₃₆O₅S 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: 86.0%

: 100-39-0
benzyl bromide

: 182624-93-7
((1S,2S,3R,6R)-2-Benzenesulfonylmethyl-6-methoxymethoxymethyl-2,3-dimethyl-cyclohexyl)-methanol

: 182625-04-3
C₂₆H₃₆O₅S

Guidance literature:: With sodium hydride; In tetrahydrofuran; N,N-dimethyl-formamide; Ambient temperature;
DOI:10.1016/0040-4039(96)01585-7

Reference yield:

: 182625-02-1
[(1S,2S,3R,6R)-2-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-3-methoxymethoxymethyl-1,6-dimethyl-cyclohexyl]-methanol

: 182625-04-3
C₂₆H₃₆O₅S

Guidance literature:: Multi-step reaction with 6 steps

1: Bu₃P, N-phenylthiosuccinimide / pyridine / 50 °C

2: OXONE / tetrahydrofuran; methanol; H₂O

3: 80percent AcOH / 50 °C

4: NaIO₄, (NH₄)2SO₄ / methanol; H₂O / 0 °C

5: NaBH₄ / methanol / 0 °C

6: 86 percent / NaH / tetrahydrofuran; dimethylformamide / Ambient temperature

With Oxone; ammonium sulfate; sodium tetrahydroborate; sodium periodate; N-(phenylthio)succinimide; tributylphosphine; sodium hydride; acetic acid; In tetrahydrofuran; pyridine; methanol; water; N,N-dimethyl-formamide;
DOI:10.1016/0040-4039(96)01585-7

Reference yield:

: 182624-80-2
[(1S,2S,3R,6S)-2-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-6-hydroxymethyl-3-methoxymethoxymethyl-1-methyl-cyclohexyl]-methanol

: 182625-04-3
C₂₆H₃₆O₅S

Guidance literature:: Multi-step reaction with 14 steps

1: 75 percent / pyridine / 0 °C

2: imidazole / dimethylformamide / Ambient temperature

3: DIBAL-H / toluene / -78 °C

4: PDC, 4 Angstroem molecular sieves / CH₂Cl₂ / Ambient temperature

5: 1.) K₂CO₃; 2.) NaBH₄ / 1.) MeOH, RT; 2.) MeOH, 0 deg C

6: 96 percent / Bu₃P / pyridine / Ambient temperature

7: 84 percent / Li / tetrahydrofuran; liquid ammonia / -34 °C

8: Bu₄NF / tetrahydrofuran / Ambient temperature

9: Bu₃P, N-phenylthiosuccinimide / pyridine / 50 °C

10: OXONE / tetrahydrofuran; methanol; H₂O

11: 80percent AcOH / 50 °C

12: NaIO₄, (NH₄)2SO₄ / methanol; H₂O / 0 °C

13: NaBH₄ / methanol / 0 °C

14: 86 percent / NaH / tetrahydrofuran; dimethylformamide / Ambient temperature

With 1H-imidazole; Oxone; ammonium sulfate; sodium tetrahydroborate; sodium periodate; dipyridinium dichromate; N-(phenylthio)succinimide; tributylphosphine; 4 A molecular sieve; tetrabutyl ammonium fluoride; lithium; sodium hydride; diisobutylaluminium hydride; potassium carbonate; acetic acid; In tetrahydrofuran; pyridine; methanol; dichloromethane; ammonia; water; N,N-dimethyl-formamide; toluene;
DOI:10.1016/0040-4039(96)01585-7