C₅₇H₈₂N₆O₁₃

Base Information

Chemical Name:C₅₇H₈₂N₆O₁₃
CAS No.:259093-41-9
Molecular Formula:C₅₇H₈₂N₆O₁₃
Molecular Weight:1059.31
Hs Code.:

C<sub>57</sub>H<sub>82</sub>N<sub>6</sub>O<sub>13</sub>

Synonyms:C₅₇H₈₂N₆O₁₃

Suppliers and Price of C₅₇H₈₂N₆O₁₃

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of C₅₇H₈₂N₆O₁₃

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₅₇H₈₂N₆O₁₃

There total 19 articles about C₅₇H₈₂N₆O₁₃ 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:

: 2051-96-9,56777-24-3,74094-05-6
benzyl (R)-Lactate

: 259093-41-9
C₅₇H₈₂N₆O₁₃

Guidance literature:: Multi-step reaction with 7 steps

1: Et₃N / tetrahydrofuran; toluene / 0 - 20 °C

2: Et₃N / tetrahydrofuran / 12 h / 20 °C

3: 78 percent / TFA / CH₂Cl₂ / 24 h / 20 °C

4: (i-Pr)2NEt; N,N'-bis(2-oxo-3-oxazolidinyl)phosphinic chloride / CH₂Cl₂ / 0 - 20 °C

5: TFA / CH₂Cl₂ / 15 h / 20 °C

6: N-methylmorpholine; N,N'-bis(2-oxo-3-oxazolidinyl)phosphinic chloride / CH₂Cl₂ / 12 h / 20 °C

7: TFA / CH₂Cl₂ / 12 h / 0 °C

With 4-methyl-morpholine; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; triethylamine; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; toluene;
DOI:10.1021/jo001749v

Reference yield:

: 197635-07-7
1-tert-butoxycarbonyl-1-methyl-2-sec-butyl-hydrazine

: 259093-41-9
C₅₇H₈₂N₆O₁₃

Guidance literature:: Multi-step reaction with 6 steps

1: Et₃N / tetrahydrofuran / 12 h / 20 °C

2: 78 percent / TFA / CH₂Cl₂ / 24 h / 20 °C

3: (i-Pr)2NEt; N,N'-bis(2-oxo-3-oxazolidinyl)phosphinic chloride / CH₂Cl₂ / 0 - 20 °C

4: TFA / CH₂Cl₂ / 15 h / 20 °C

5: N-methylmorpholine; N,N'-bis(2-oxo-3-oxazolidinyl)phosphinic chloride / CH₂Cl₂ / 12 h / 20 °C

6: TFA / CH₂Cl₂ / 12 h / 0 °C

With 4-methyl-morpholine; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; triethylamine; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jo001749v

Reference yield:

: N'-isobutylidene-N-methyl-hydrazinecarboxylic acid tert-butyl ester

: 259093-41-9
C₅₇H₈₂N₆O₁₃

Guidance literature:: Multi-step reaction with 7 steps

1: NaCNBH₃; AcOH / methanol / 0 °C / pH 3 - 4

2: Et₃N / tetrahydrofuran / 12 h / 20 °C

3: 78 percent / TFA / CH₂Cl₂ / 24 h / 20 °C

4: (i-Pr)2NEt; N,N'-bis(2-oxo-3-oxazolidinyl)phosphinic chloride / CH₂Cl₂ / 0 - 20 °C

5: TFA / CH₂Cl₂ / 15 h / 20 °C

6: N-methylmorpholine; N,N'-bis(2-oxo-3-oxazolidinyl)phosphinic chloride / CH₂Cl₂ / 12 h / 20 °C

7: TFA / CH₂Cl₂ / 12 h / 0 °C

With 4-methyl-morpholine; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; sodium cyanoborohydride; acetic acid; triethylamine; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1021/jo001749v