C₅₈H₈₈O₁₀Si₂

Base Information

Chemical Name:C₅₈H₈₈O₁₀Si₂
CAS No.:220691-96-3
Molecular Formula:C₅₈H₈₈O₁₀Si₂
Molecular Weight:1001.5
Hs Code.:

C<sub>58</sub>H<sub>88</sub>O<sub>10</sub>Si<sub>2</sub>

Synonyms:C₅₈H₈₈O₁₀Si₂

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Chemical Property of C₅₈H₈₈O₁₀Si₂

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Technology Process of C₅₈H₈₈O₁₀Si₂

There total 35 articles about C₅₈H₈₈O₁₀Si₂ 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: 95.0%

: 220691-31-6
C₆₅H₉₄O₁₀Si₂

: 220691-96-3
C₅₈H₈₈O₁₀Si₂

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol; dichloromethane;

Reference yield:

: 52813-63-5
(5R)-2,3,4,5-tetrahydro-5-hydroxymethyl-2-furanone

: 220691-96-3
C₅₈H₈₈O₁₀Si₂

Guidance literature:: Multi-step reaction with 13 steps

1: 84 percent / Ph₃P, DEAD / tetrahydrofuran / Heating

2: 98 percent / DIBAL-H / toluene / -78 °C

3: acetonitrile

4: NaOH / H₂O / Heating

5: 1.) LDA, 2.) t-BuOK / 1.) THF, -78 deg C, 2.) THF, -78 deg C to r.t.

6: H₂O, TFA / CH₂Cl₂

7: 87 percent / imidazole / dimethylformamide

8: 96 percent / MCPBA, NaOAc / CH₂Cl₂ / 0 °C

9: 1.) BuLi, Me₂AlCl / 1.) PhMe, 0 deg C; CH₂Cl₂, 0 deg C to r.t., 2.) PhMe, CH₂Cl₂

10: 1.) 9-BBN, 2.) NaOH, H₂O₂ / 1.) THF, reflux, 2.) THF, H₂O₂, r.t.

11: NaBH₄ / ethanol / 0 °C

12: 95 percent / 2,6-lutidine / CH₂Cl₂

13: 95 percent / H₂ / Pd/C / methanol; CH₂Cl₂

With 1H-imidazole; 2,6-dimethylpyridine; sodium hydroxide; sodium tetrahydroborate; 9-borabicyclo[3.3.1]nonane dimer; n-butyllithium; potassium tert-butylate; water; hydrogen; dihydrogen peroxide; sodium acetate; dimethylaluminum chloride; diisobutylaluminium hydride; 3-chloro-benzenecarboperoxoic acid; triphenylphosphine; trifluoroacetic acid; lithium diisopropyl amide; diethylazodicarboxylate; palladium on activated charcoal; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide; toluene; acetonitrile;

Reference yield:

: 106357-31-7
(2S,3S,4R)-1-benzyloxy-2,4-dimethylhex-5-ene-3-ol

: 220691-96-3
C₅₈H₈₈O₁₀Si₂

Guidance literature:: Multi-step reaction with 16 steps

1: 1.) 9-BBN, 2.) NaOH, H₂O₂ / 1.) THF, 65 deg C, 2.) THF, H₂O, 0 deg C to r.t.

2: 96 percent / PPTS / CH₂Cl₂

3: Na, NH₃ / diethyl ether

4: PPTS / CH₂Cl₂

5: Et₃N / CH₂Cl₂ / -5 °C

6: NaI, molecular sieves 4 Angstroem / butan-2-one / 45 °C

7: 1.) BuLi, DMPU / 1.) THF, -78 deg C, 2.) THF

8: CSA / methanol

9: TPAP, NMO, molecular sieves 4 Angstroem / CH₂Cl₂

10: Ph₃P / 0 °C

11: BuLi

12: 1.) BuLi, Me₂AlCl / 1.) PhMe, 0 deg C; CH₂Cl₂, 0 deg C to r.t., 2.) PhMe, CH₂Cl₂

13: 1.) 9-BBN, 2.) NaOH, H₂O₂ / 1.) THF, reflux, 2.) THF, H₂O₂, r.t.

14: NaBH₄ / ethanol / 0 °C

15: 95 percent / 2,6-lutidine / CH₂Cl₂

16: 95 percent / H₂ / Pd/C / methanol; CH₂Cl₂

With 2,6-dimethylpyridine; 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; sodium hydroxide; sodium tetrahydroborate; 9-borabicyclo[3.3.1]nonane dimer; n-butyllithium; N-methyl-2-indolinone; tetrapropylammonium perruthennate; 4 A molecular sieve; camphor-10-sulfonic acid; ammonia; hydrogen; dihydrogen peroxide; sodium; dimethylaluminum chloride; pyridinium p-toluenesulfonate; triethylamine; triphenylphosphine; sodium iodide; palladium on activated charcoal; In methanol; diethyl ether; ethanol; dichloromethane; butanone;