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tert-butyloxycarbonyl-alanyl-aminoisobutyryl-alanyl methyl ester

Base Information
  • Chemical Name:tert-butyloxycarbonyl-alanyl-aminoisobutyryl-alanyl methyl ester
  • CAS No.:72086-86-3
  • Molecular Formula:C16H29 N3 O6
  • Molecular Weight:359.42
  • Hs Code.:
  • Mol file:72086-86-3.mol
tert-butyloxycarbonyl-alanyl-aminoisobutyryl-alanyl methyl ester

Synonyms:L-Alanine,N-[N-[N-[(1,1-dimethylethoxy)carbonyl]-L-alanyl]-2-methylalanyl]-, methyl ester

Suppliers and Price of tert-butyloxycarbonyl-alanyl-aminoisobutyryl-alanyl methyl ester
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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  • Chemicals and raw materials
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Total 3 raw suppliers
Chemical Property of tert-butyloxycarbonyl-alanyl-aminoisobutyryl-alanyl methyl ester
Chemical Property:
  • Vapor Pressure:2.15E-09mmHg at 25°C 
  • Boiling Point:480.5°C at 760 mmHg 
  • Flash Point:244.4°C 
  • Density:1.143g/cm3 
Purity/Quality:

99% *data from raw suppliers

Safty Information:
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  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of tert-butyloxycarbonyl-alanyl-aminoisobutyryl-alanyl methyl ester

There total 8 articles about tert-butyloxycarbonyl-alanyl-aminoisobutyryl-alanyl methyl ester 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:
Guidance literature:
With dicyclohexyl-carbodiimide; In dichloromethane; Ambient temperature;
DOI:10.1016/S0040-4020(01)92061-7
Guidance literature:
With 4-methyl-morpholine; dicyclohexyl-carbodiimide; In dichloromethane; Ambient temperature;
DOI:10.1016/S0040-4020(01)88119-9
Guidance literature:
Multi-step reaction with 5 steps
1: N-methylmorpholine / tetrahydrofuran / -15 °C
2: tetrahydrofuran / Ambient temperature
3: H2 / Pd/C / ethanol / 760 Torr
4: N-methylmorpholine / tetrahydrofuran / -15 °C
5: tetrahydrofuran / Ambient temperature
With 4-methyl-morpholine; hydrogen; palladium on activated charcoal; In tetrahydrofuran; ethanol;
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