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TERT-BUTYL (3S)-3-AMINOBUTANOATE

Base Information
  • Chemical Name:TERT-BUTYL (3S)-3-AMINOBUTANOATE
  • CAS No.:161105-54-0
  • Molecular Formula:C8H17 N O2
  • Molecular Weight:159.228
  • Hs Code.:29224985
  • Mol file:161105-54-0.mol
TERT-BUTYL (3S)-3-AMINOBUTANOATE

Synonyms:Butanoicacid, 3-amino-, 1,1-dimethylethyl ester, (S)-; 1,1-Dimethylethyl(S)-3-aminobutanoate

Suppliers and Price of TERT-BUTYL (3S)-3-AMINOBUTANOATE
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
  • TRC
  • 3-Amino-butyricacidtert-butylester
  • 100mg
  • $ 175.00
  • American Custom Chemicals Corporation
  • (S)-3-AMINO-BUTYRIC ACID TERT-BUTYL ESTER 95.00%
  • 1G
  • $ 1963.50
  • American Custom Chemicals Corporation
  • (S)-3-AMINO-BUTYRIC ACID TERT-BUTYL ESTER 95.00%
  • 100MG
  • $ 175.84
Total 9 raw suppliers
Chemical Property of TERT-BUTYL (3S)-3-AMINOBUTANOATE
Chemical Property:
  • Vapor Pressure:0.23mmHg at 25°C 
  • Refractive Index:1.423-1.427 
  • Boiling Point:207.1°Cat760mmHg 
  • PKA:8.71±0.10(Predicted) 
  • Flash Point:76.9°C 
  • PSA:52.32000 
  • Density:g/cm3 
  • LogP:1.76570 
Purity/Quality:

98%Min *data from raw suppliers

3-Amino-butyricacidtert-butylester *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes:
  • Statements: 34 
  • Safety Statements: 45-36/37/39-26 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of TERT-BUTYL (3S)-3-AMINOBUTANOATE

There total 11 articles about TERT-BUTYL (3S)-3-AMINOBUTANOATE 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 hydrogen; palladium dihydroxide; In methanol; for 24h; under 1551.44 Torr;
DOI:10.1021/jo0349633
Guidance literature:
Multi-step reaction with 2 steps
1.1: n-BuLi / tetrahydrofuran; hexane / 0.5 h / -78 °C
1.2: 87 percent / tetrahydrofuran; hexane / 3 h / -78 °C
2.1: 73 percent / H2; acetic acid / Pd(OH)2/C / methanol; H2O / 24 h / 20 °C / 760.05 Torr
With n-butyllithium; hydrogen; acetic acid; palladium dihydroxide; In tetrahydrofuran; methanol; hexane; water;
DOI:10.1016/j.tetasy.2007.06.008
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