S-2-(2-(benzyloxycarbonylamino)-2-methylpropylthio)ethyl ethanethioate

Base Information

Chemical Name:S-2-(2-(benzyloxycarbonylamino)-2-methylpropylthio)ethyl ethanethioate
CAS No.:1037833-02-5
Molecular Formula:C₁₆H₂₃NO₃S₂
Molecular Weight:341.496
Hs Code.:

Synonyms:S-2-(2-(benzyloxycarbonylamino)-2-methylpropylthio)ethyl ethanethioate

Suppliers and Price of S-2-(2-(benzyloxycarbonylamino)-2-methylpropylthio)ethyl ethanethioate

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 S-2-(2-(benzyloxycarbonylamino)-2-methylpropylthio)ethyl ethanethioate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of S-2-(2-(benzyloxycarbonylamino)-2-methylpropylthio)ethyl ethanethioate

There total 3 articles about S-2-(2-(benzyloxycarbonylamino)-2-methylpropylthio)ethyl ethanethioate 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:

: 1037833-00-3
benzyl 1-mercapto-2-methylpropan-2-ylcarbamate

: 1037833-02-5
S-2-(2-(benzyloxycarbonylamino)-2-methylpropylthio)ethyl ethanethioate

Guidance literature:: Multi-step reaction with 2 steps

1: caesium carbonate / N,N-dimethyl-formamide / 16 h

2: N,N-dimethyl-formamide / 70 °C

With caesium carbonate; In N,N-dimethyl-formamide;

Reference yield:

: 62471-40-3
2-benzyloxycarbonylamino-2-methylpropanol

: 1037833-02-5
S-2-(2-(benzyloxycarbonylamino)-2-methylpropylthio)ethyl ethanethioate

Guidance literature:: Multi-step reaction with 4 steps

1: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / -5 °C

2: sodium hydroxide / methanol; water / 0.25 h / 20 °C

3: caesium carbonate / N,N-dimethyl-formamide / 16 h

4: N,N-dimethyl-formamide / 70 °C

With sodium hydroxide; di-isopropyl azodicarboxylate; caesium carbonate; triphenylphosphine; In tetrahydrofuran; methanol; water; N,N-dimethyl-formamide; 1: Mitsunobu reaction;

Reference yield:

: 1032764-10-5
2-(benzyloxycarbonyl)amino-2-methylpropyl thioacetate

: 1037833-02-5
S-2-(2-(benzyloxycarbonylamino)-2-methylpropylthio)ethyl ethanethioate

Guidance literature:: Multi-step reaction with 3 steps

1: sodium hydroxide / methanol; water / 0.25 h / 20 °C

2: caesium carbonate / N,N-dimethyl-formamide / 16 h

3: N,N-dimethyl-formamide / 70 °C

With sodium hydroxide; caesium carbonate; In methanol; water; N,N-dimethyl-formamide;