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Boc-L-aspartic acid ss-benzyl ester Merrifield resin

Base Information
  • Chemical Name:Boc-L-aspartic acid ss-benzyl ester Merrifield resin
  • CAS No.:79069-52-6
  • Molecular Formula:C16H21NO5
  • Molecular Weight:307.346
  • Hs Code.:
  • DSSTox Substance ID:DTXSID801148891
  • Nikkaji Number:J1.238.818G
Boc-L-aspartic acid ss-benzyl ester Merrifield resin

Synonyms:SCHEMBL1261930;DTXSID801148891;MFCD00801164;79069-52-6;Boc-L-Asp(Bzl)-PAM resin (100-200 mesh);Boc-L-aspartic acid ss-benzyl ester Merrifield resin;Phenylmethyl (3S)-3-[[(1,1-dimethylethoxy)carbonyl]amino]-4-oxobutanoate;Boc-L-aspartic acid b-benzyl ester 4-oxymethylphenylacetamidomethyl resin 100-200mesh 0.25-1.0 meq/g

Suppliers and Price of Boc-L-aspartic acid ss-benzyl ester Merrifield resin
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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Chemical Property of Boc-L-aspartic acid ss-benzyl ester Merrifield resin
Chemical Property:
  • Boiling Point:451.3±45.0 °C(Predicted) 
  • PSA:81.70000 
  • Density:1.147±0.06 g/cm3(Predicted) 
  • LogP:2.60300 
  • XLogP3:1.8
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:9
  • Exact Mass:307.14197277
  • Heavy Atom Count:22
  • Complexity:383
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)(C)OC(=O)NC(CC(=O)OCC1=CC=CC=C1)C=O
  • Isomeric SMILES:CC(C)(C)OC(=O)N[C@@H](CC(=O)OCC1=CC=CC=C1)C=O
Technology Process of Boc-L-aspartic acid ss-benzyl ester Merrifield resin

There total 5 articles about Boc-L-aspartic acid ss-benzyl ester Merrifield resin 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 dipyridinium dichromate; In dichloromethane; Ambient temperature;
DOI:10.1021/jo00336a039
Guidance literature:
With hydrogen; palladium on activated charcoal; In 1,2-dimethoxyethane; ethanol; at 20 ℃; for 3h;
DOI:10.1021/jo991112f
Guidance literature:
Multi-step reaction with 2 steps
1.1: iBuOCOCl; NMM / tetrahydrofuran / -10 °C
1.2: aq. NaBH4 / tetrahydrofuran
2.1: Dess-Martin periodinane / CH2Cl2
With 4-methyl-morpholine; Dess-Martin periodane; isobutyl chloroformate; In tetrahydrofuran; dichloromethane;
DOI:10.1016/j.bmcl.2005.12.056
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