C₅₆H₇₄O₂₅

Base Information

Chemical Name:C₅₆H₇₄O₂₅
CAS No.:189144-74-9
Molecular Formula:C₅₆H₇₄O₂₅
Molecular Weight:1147.19
Hs Code.:

C<sub>56</sub>H<sub>74</sub>O<sub>25</sub>

Synonyms:C₅₆H₇₄O₂₅

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Chemical Property of C₅₆H₇₄O₂₅

Chemical Property:

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Technology Process of C₅₆H₇₄O₂₅

There total 31 articles about C₅₆H₇₄O₂₅ 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:

: 4547-43-7
methyl 6-hydroxycaproate

: 189144-74-9
C₅₆H₇₄O₂₅

Guidance literature:: Multi-step reaction with 3 steps

1: 80 percent / hex-1-ene, ethyldiisopropylamine / CH₂Cl₂ / 36 h / 23 °C

2: 83 percent / H₂, AcOH / Pd-C / ethanol / 24 h / 23 °C / 10343 Torr

3: 1.) Ag₂CO₃, 4 Angstroem molecular sieves, 2.) AgClO₄ / 1) CH₂Cl₂, 23 deg C, 1 h; 2) CH₂Cl₂, 23 deg C, 12 h

With 1-hexene; 4 A molecular sieve; hydrogen; silver perchlorate; acetic acid; N-ethyl-N,N-diisopropylamine; silver carbonate; palladium on activated charcoal; In ethanol; dichloromethane;
DOI:10.1021/jo962300y

Reference yield:

: 173398-22-6
3,4,6-tri-O-acetyl-2-O-benzyl-β-D-glucopyranosyl bromide

: 189144-74-9
C₅₆H₇₄O₂₅

Guidance literature:: Multi-step reaction with 3 steps

1: 80 percent / hex-1-ene, ethyldiisopropylamine / CH₂Cl₂ / 36 h / 23 °C

2: 83 percent / H₂, AcOH / Pd-C / ethanol / 24 h / 23 °C / 10343 Torr

3: 1.) Ag₂CO₃, 4 Angstroem molecular sieves, 2.) AgClO₄ / 1) CH₂Cl₂, 23 deg C, 1 h; 2) CH₂Cl₂, 23 deg C, 12 h

With 1-hexene; 4 A molecular sieve; hydrogen; silver perchlorate; acetic acid; N-ethyl-N,N-diisopropylamine; silver carbonate; palladium on activated charcoal; In ethanol; dichloromethane;
DOI:10.1021/jo962300y

Reference yield:

: 173314-28-8
phenyl 3,4,6-tri-O-acetyl-2-O-benzyl-1-thio-α-D-glucopyranoside

: 189144-74-9
C₅₆H₇₄O₂₅

Guidance literature:: Multi-step reaction with 4 steps

1: bromine / CH₂Cl₂ / 0.08 h / 0 - 23 °C

2: 80 percent / hex-1-ene, ethyldiisopropylamine / CH₂Cl₂ / 36 h / 23 °C

3: 83 percent / H₂, AcOH / Pd-C / ethanol / 24 h / 23 °C / 10343 Torr

4: 1.) Ag₂CO₃, 4 Angstroem molecular sieves, 2.) AgClO₄ / 1) CH₂Cl₂, 23 deg C, 1 h; 2) CH₂Cl₂, 23 deg C, 12 h

With 1-hexene; 4 A molecular sieve; hydrogen; bromine; silver perchlorate; acetic acid; N-ethyl-N,N-diisopropylamine; silver carbonate; palladium on activated charcoal; In ethanol; dichloromethane;
DOI:10.1021/jo962300y