C₂₄H₂₅N₂O₂⁽¹⁺⁾*C₇H₇O₃S^(1-)

Base Information

Chemical Name:C₂₄H₂₅N₂O₂⁽¹⁺⁾*C₇H₇O₃S^(1-)
CAS No.:88930-21-6
Molecular Formula:C₇H₇O₃S*C₂₄H₂₅N₂O₂
Molecular Weight:544.671
Hs Code.:

C<sub>24</sub>H<sub>25</sub>N<sub>2</sub>O<sub>2</sub><sup>(1+)</sup>*C<sub>7</sub>H<sub>7</sub>O<sub>3</sub>S<sup>(1-)</sup>

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Suppliers and Price of C₂₄H₂₅N₂O₂⁽¹⁺⁾*C₇H₇O₃S^(1-)

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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 C₂₄H₂₅N₂O₂⁽¹⁺⁾*C₇H₇O₃S^(1-)

Chemical Property:

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Technology Process of C₂₄H₂₅N₂O₂⁽¹⁺⁾*C₇H₇O₃S^(1-)

There total 10 articles about C₂₄H₂₅N₂O₂⁽¹⁺⁾*C₇H₇O₃S^(1-) 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:

: 88901-92-2
methyl 4,6-O-benzylidene-3-C-(carbomethoxy-methylene)-2,3-didesoxy-α-D-ribo-hexapyranoside

: 88930-21-6,88930-23-8
C₂₄H₂₅N₂O₂⁽¹⁺⁾*C₇H₇O₃S^(1-)

Guidance literature:: Multi-step reaction with 7 steps

1: 80 percent / hydrogen / 10percent Pd-C / methanol / 12 h

2: 75 percent / acetyl chloride / 24 h / Heating

3: 98 percent / aq. NaIO₄, NaHCO₃ / ethanol / 24 h / 20 °C

4: 84 percent / NaBH₄ / methanol / 0 - 10 °C

5: 97 percent / 33percent aq. acetic acid / 48 h / 120 °C

6: 56 percent / acetic acid / benzene / 1 h / Heating

7: p-toluenesulfonyl chloride, pyridine / 24 h / 20 °C

With pyridine; sodium tetrahydroborate; sodium periodate; hydrogen; sodium hydrogencarbonate; acetic acid; acetyl chloride; p-toluenesulfonyl chloride; palladium on activated charcoal; In methanol; ethanol; benzene;
DOI:10.1016/S0040-4020(01)80014-4

Reference yield:

: 88901-86-4,88901-87-5
<γR(1'S),(1R,1S)>-acide-δ-<1-(Nb-benzyl-tetrahydro-β-carboline)>-γ-<1'-(1',2'-dihydroxyethyl)>-butyrique-1',α,γ-lactone

: 88930-21-6,88930-23-8
C₂₄H₂₅N₂O₂⁽¹⁺⁾*C₇H₇O₃S^(1-)

Guidance literature:: With pyridine; p-toluenesulfonyl chloride; at 20 ℃; for 24h;
DOI:10.1016/S0040-4020(01)80014-4

Reference yield:

: 136945-86-3,137036-19-2
3-C-(carboxy-methylene)-2,3-didesoxy-α-β-D-erythro-pentapyranose

: 88930-21-6,88930-23-8
C₂₄H₂₅N₂O₂⁽¹⁺⁾*C₇H₇O₃S^(1-)

Guidance literature:: Multi-step reaction with 2 steps

1: 56 percent / acetic acid / benzene / 1 h / Heating

2: p-toluenesulfonyl chloride, pyridine / 24 h / 20 °C

With pyridine; acetic acid; p-toluenesulfonyl chloride; In benzene;
DOI:10.1016/S0040-4020(01)80014-4