C₅₁H₅₆O₁₇

Base Information

Chemical Name:C₅₁H₅₆O₁₇
CAS No.:130719-12-9
Molecular Formula:C₅₁H₅₆O₁₇
Molecular Weight:940.995
Hs Code.:

C<sub>51</sub>H<sub>56</sub>O<sub>17</sub>

Synonyms:C₅₁H₅₆O₁₇

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Chemical Property of C₅₁H₅₆O₁₇

Chemical Property:

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Technology Process of C₅₁H₅₆O₁₇

There total 8 articles about C₅₁H₅₆O₁₇ 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: 80.0%

: 130719-11-8
methyl 5-O-(2,3-di-O-benzoyl-5-O-(chloroacetyl)-6-O-pivaloyl-β-D-galactofuranosyl)-2,3-di-O-benzoyl-6-O-pivaloyl-β-D-galactofuranoside

: 130719-12-9
C₅₁H₅₆O₁₇

Guidance literature:: With hydrazinium monoacetate; In methanol; water; at 50 ℃; for 4h;

Reference yield:

: 130719-06-1
ethyl 5,6-O-isopropylidene-1-thio-α-D-galactofuranoside

: 130719-12-9
C₅₁H₅₆O₁₇

Guidance literature:: Multi-step reaction with 8 steps

1: pyridine / 1 h / 0 °C

2: HOAc, H₂O / 4 h / 60 °C

3: 89 percent / pyridine / dioxane / 1 h / 0 °C

4: 95 percent / NaHCO₃ / dimethylformamide / 2 h / 20 °C

5: 84 percent / N-iodosuccinimide / trifluoromethanesulfonic acid / 1,2-dichloro-ethane / 0.08 h / 20 °C

6: 87 percent / hydrazine acetate / methanol; H₂O / 4 h / 50 °C

7: 95 percent / N-iodosuccinimide / trifluoromethanesulfonic acid / 1,2-dichloro-ethane / 0.08 h / 0 °C

8: 80 percent / hydrazine acetate / methanol; H₂O / 4 h / 50 °C

With pyridine; N-iodo-succinimide; water; hydrazinium monoacetate; sodium hydrogencarbonate; acetic acid; trifluorormethanesulfonic acid; In 1,4-dioxane; methanol; water; 1,2-dichloro-ethane; N,N-dimethyl-formamide;

Reference yield:

: 99773-30-5
5,6-O-isopropylidene-D-galactose diethyl dithioacetal

: 130719-12-9
C₅₁H₅₆O₁₇

Guidance literature:: Multi-step reaction with 9 steps

1: 63 percent / molecular sieves 4 Angstroem, HgCl₂, HgO / acetonitrile / 0.08 h / 20 °C

2: pyridine / 1 h / 0 °C

3: HOAc, H₂O / 4 h / 60 °C

4: 89 percent / pyridine / dioxane / 1 h / 0 °C

5: 95 percent / NaHCO₃ / dimethylformamide / 2 h / 20 °C

6: 84 percent / N-iodosuccinimide / trifluoromethanesulfonic acid / 1,2-dichloro-ethane / 0.08 h / 20 °C

7: 87 percent / hydrazine acetate / methanol; H₂O / 4 h / 50 °C

8: 95 percent / N-iodosuccinimide / trifluoromethanesulfonic acid / 1,2-dichloro-ethane / 0.08 h / 0 °C

9: 80 percent / hydrazine acetate / methanol; H₂O / 4 h / 50 °C

With pyridine; N-iodo-succinimide; 4 A molecular sieve; water; hydrazinium monoacetate; sodium hydrogencarbonate; acetic acid; mercury dichloride; mercury(II) oxide; trifluorormethanesulfonic acid; In 1,4-dioxane; methanol; water; 1,2-dichloro-ethane; N,N-dimethyl-formamide; acetonitrile;