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BOC-(RS)-2-AMINO-4-BENZYLOXYBUTANOIC ACID

Base Information
  • Chemical Name:BOC-(RS)-2-AMINO-4-BENZYLOXYBUTANOIC ACID
  • CAS No.:876617-13-9
  • Molecular Formula:C16H23NO5
  • Molecular Weight:309.362
  • Hs Code.:
  • Mol file:876617-13-9.mol
BOC-(RS)-2-AMINO-4-BENZYLOXYBUTANOIC ACID

Synonyms:L-2-(tert-Butoxycarbonylamino)-4-(benzyloxy)butanoic acid

Suppliers and Price of BOC-(RS)-2-AMINO-4-BENZYLOXYBUTANOIC ACID
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
  • Matrix Scientific
  • Boc-DL-Hse(Bzl)-OH
  • 5g
  • $ 785.00
  • Matrix Scientific
  • Boc-DL-Hse(Bzl)-OH
  • 1g
  • $ 212.00
  • American Custom Chemicals Corporation
  • BOC-DL-HSE(BZL)-OH 95.00%
  • 1G
  • $ 423.15
  • AK Scientific
  • Boc-DL-Hse(Bzl)-OH
  • 1g
  • $ 336.00
  • Activate Scientific
  • N-Boc-O-benzyl-DL-homoserine 95+%
  • 1 g
  • $ 450.00
  • Activate Scientific
  • N-Boc-O-benzyl-DL-homoserine 95+%
  • 250 mg
  • $ 212.00
  • Acrotein
  • N-Boc-O-benzyl-DL-homoserine 97%
  • 1g
  • $ 275.00
Total 7 raw suppliers
Chemical Property of BOC-(RS)-2-AMINO-4-BENZYLOXYBUTANOIC ACID
Chemical Property:
Purity/Quality:

97% *data from raw suppliers

Boc-DL-Hse(Bzl)-OH *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of BOC-(RS)-2-AMINO-4-BENZYLOXYBUTANOIC ACID

There total 2 articles about BOC-(RS)-2-AMINO-4-BENZYLOXYBUTANOIC ACID 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:
Multi-step reaction with 2 steps
1: sodium hydroxide / ethanol; water; tetrahydrofuran / 24 h / 20 °C / Cooling with ice
2: triethylamine / acetone / 6 h / 55 °C
With triethylamine; sodium hydroxide; In tetrahydrofuran; ethanol; water; acetone;
Guidance literature:
With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 20 ℃;
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