C₅₇H₇₆N₆O₁₂

Base Information

Chemical Name:C₅₇H₇₆N₆O₁₂
CAS No.:573968-38-4
Molecular Formula:C₅₇H₇₆N₆O₁₂
Molecular Weight:1037.26
Hs Code.:

C<sub>57</sub>H<sub>76</sub>N<sub>6</sub>O<sub>12</sub>

Synonyms:

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Chemical Property of C₅₇H₇₆N₆O₁₂

Chemical Property:

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Technology Process of C₅₇H₇₆N₆O₁₂

There total 8 articles about C₅₇H₇₆N₆O₁₂ 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:

: 621-44-3
3-nitro-L-tyrosine

: 573968-38-4
C₅₇H₇₆N₆O₁₂

Guidance literature:: Multi-step reaction with 9 steps

1: AcCl

2: HBTU; DIPEA / 4 h / 20 °C

3: 88 percent / NaHCO₃ / N,N-dimethyl-acetamide / 2 h / 90 °C

4: cyclohexene / 10 percent Pd/C / ethanol / 24 h / Heating

5: 1.0 g / DIPEA / CH₂Cl₂ / 1.5 h

6: LiBH₄ / tetrahydrofuran; methanol / 3 h / 20 °C

7: TEMPO; PhI(OAc)2 / CH₂Cl₂ / 2 h / 20 °C

8: Zn; VCl₃(thf)3 / CH₂Cl₂ / 5 h / 20 °C

9: 0.30 g / TsOH / CH₂Cl₂ / 1 h

With 2,2,6,6-tetramethyl-piperidine-N-oxyl; lithium borohydride; Vanadium (III) chloride-(tris-tetrahydrofuran); [bis(acetoxy)iodo]benzene; sodium hydrogencarbonate; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; toluene-4-sulfonic acid; N-ethyl-N,N-diisopropylamine; acetyl chloride; zinc; cyclohexene; palladium on activated charcoal; In tetrahydrofuran; methanol; ethanol; dichloromethane; N,N-dimethyl acetamide;
DOI:10.1016/S0968-0896(03)00054-3

Reference yield:

: 3195-65-1
methyl 3-nitro-L-tyrosinate

: 573968-38-4
C₅₇H₇₆N₆O₁₂

Guidance literature:: Multi-step reaction with 8 steps

1: HBTU; DIPEA / 4 h / 20 °C

2: 88 percent / NaHCO₃ / N,N-dimethyl-acetamide / 2 h / 90 °C

3: cyclohexene / 10 percent Pd/C / ethanol / 24 h / Heating

4: 1.0 g / DIPEA / CH₂Cl₂ / 1.5 h

5: LiBH₄ / tetrahydrofuran; methanol / 3 h / 20 °C

6: TEMPO; PhI(OAc)2 / CH₂Cl₂ / 2 h / 20 °C

7: Zn; VCl₃(thf)3 / CH₂Cl₂ / 5 h / 20 °C

8: 0.30 g / TsOH / CH₂Cl₂ / 1 h

With 2,2,6,6-tetramethyl-piperidine-N-oxyl; lithium borohydride; Vanadium (III) chloride-(tris-tetrahydrofuran); [bis(acetoxy)iodo]benzene; sodium hydrogencarbonate; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; toluene-4-sulfonic acid; N-ethyl-N,N-diisopropylamine; zinc; cyclohexene; palladium on activated charcoal; In tetrahydrofuran; methanol; ethanol; dichloromethane; N,N-dimethyl acetamide;
DOI:10.1016/S0968-0896(03)00054-3

Reference yield:

: 573968-33-9
(S)-2-((S)-2-tert-Butoxycarbonylamino-3-methyl-butyrylamino)-3-(4-hydroxy-3-nitro-phenyl)-propionic acid methyl ester

: 573968-38-4
C₅₇H₇₆N₆O₁₂

Guidance literature:: Multi-step reaction with 7 steps

1: 88 percent / NaHCO₃ / N,N-dimethyl-acetamide / 2 h / 90 °C

2: cyclohexene / 10 percent Pd/C / ethanol / 24 h / Heating

3: 1.0 g / DIPEA / CH₂Cl₂ / 1.5 h

4: LiBH₄ / tetrahydrofuran; methanol / 3 h / 20 °C

5: TEMPO; PhI(OAc)2 / CH₂Cl₂ / 2 h / 20 °C

6: Zn; VCl₃(thf)3 / CH₂Cl₂ / 5 h / 20 °C

7: 0.30 g / TsOH / CH₂Cl₂ / 1 h

With 2,2,6,6-tetramethyl-piperidine-N-oxyl; lithium borohydride; Vanadium (III) chloride-(tris-tetrahydrofuran); [bis(acetoxy)iodo]benzene; sodium hydrogencarbonate; toluene-4-sulfonic acid; N-ethyl-N,N-diisopropylamine; zinc; cyclohexene; palladium on activated charcoal; In tetrahydrofuran; methanol; ethanol; dichloromethane; N,N-dimethyl acetamide;
DOI:10.1016/S0968-0896(03)00054-3