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BOC-GLU(OAL)-OAL

Base Information Edit
  • Chemical Name:BOC-GLU(OAL)-OAL
  • CAS No.:212569-21-6
  • Molecular Formula:C16H25NO6
  • Molecular Weight:327.37300
  • Hs Code.:
  • Mol file:212569-21-6.mol
BOC-GLU(OAL)-OAL

Synonyms:

Suppliers and Price of BOC-GLU(OAL)-OAL
Supply Marketing:Edit
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
  • Crysdot
  • (S)-Diallyl2-((tert-butoxycarbonyl)amino)pentanedioate 95+%
  • 5g
  • $ 698.00
  • Chemenu
  • (S)-Diallyl2-((tert-butoxycarbonyl)amino)pentanedioate 95%
  • 5g
  • $ 659.00
Total 7 raw suppliers
Chemical Property of BOC-GLU(OAL)-OAL Edit
Chemical Property:
  • Boiling Point:420.9±45.0 °C(Predicted) 
  • PKA:10.96±0.46(Predicted) 
  • PSA:90.93000 
  • Density:1.082±0.06 g/cm3(Predicted) 
  • LogP:2.50920 
Purity/Quality:

99% *data from raw suppliers

(S)-Diallyl2-((tert-butoxycarbonyl)amino)pentanedioate 95+% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of BOC-GLU(OAL)-OAL

There total 1 articles about BOC-GLU(OAL)-OAL 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 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; for 24h;
DOI:10.1016/j.tetlet.2009.03.130
Guidance literature:
With Alcalase-cross-linked-enzyme-aggregates; In tert-butyl alcohol; at 37 ℃; for 16h; pH=7.5; regioselective reaction; aq. phosphate buffer; Enzymatic reaction;
DOI:10.1016/j.tetlet.2009.03.130
upstream raw materials:

Boc-Glu

allyl alcohol

Downstream raw materials:

N-α-(t-butoxycarbonyl)-L-glutamic γ-allyl ester

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