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BOC-BETA-N-BENZYLAMINO-L-ALA

Base Information
  • Chemical Name:BOC-BETA-N-BENZYLAMINO-L-ALA
  • CAS No.:124730-06-9
  • Molecular Formula:C15H22N2O4
  • Molecular Weight:294.351
  • Hs Code.:
  • Mol file:124730-06-9.mol
BOC-BETA-N-BENZYLAMINO-L-ALA

Synonyms:BOC-BETA-N-BENZYLAMINO-L-ALA;BOC-(S)-2-AMINO-3-(BENZYLAMINO)PROPANOIC ACID;Boc-Bata-N-Benzylamino-L-Ala

Suppliers and Price of BOC-BETA-N-BENZYLAMINO-L-ALA
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
  • American Custom Chemicals Corporation
  • BOC-BETA-N-BENZYLAMINO-L-ALA 98.00%
  • 5MG
  • $ 500.79
Total 6 raw suppliers
Chemical Property of BOC-BETA-N-BENZYLAMINO-L-ALA
Chemical Property:
  • Boiling Point:473.2±45.0 °C(Predicted) 
  • PKA:2.88±0.18(Predicted) 
  • PSA:87.66000 
  • Density:1.159±0.06 g/cm3(Predicted) 
  • LogP:2.53590 
Purity/Quality:

99%, *data from raw suppliers

BOC-BETA-N-BENZYLAMINO-L-ALA 98.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of BOC-BETA-N-BENZYLAMINO-L-ALA

There total 9 articles about BOC-BETA-N-BENZYLAMINO-L-ALA 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 sodium tetrahydroborate; triethylamine; In methanol; at 0 ℃; for 0.666667h;
DOI:10.1016/j.bmc.2004.01.041
Guidance literature:
Multi-step reaction with 3 steps
1: sodium hydrogencarbonate; 2,2,6,6-tetramethyl-piperidine-N-oxyl; trichloroisocyanuric acid; sodium bromide / acetone / 0 - 20 °C
2: 2,2'-iminobis[ethanol] / dichloromethane / 0.5 h / 20 °C
3: sodium hydrogencarbonate / water; 1,4-dioxane / 20 °C
With 2,2,6,6-tetramethyl-piperidine-N-oxyl; trichloroisocyanuric acid; sodium hydrogencarbonate; 2,2'-iminobis[ethanol]; sodium bromide; In 1,4-dioxane; dichloromethane; water; acetone;
DOI:10.3390/molecules25061313
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