Structure

Boc-Lys(Biotin)-OH

CAS
62062-43-5
Catalog Number
ACM62062435-2
Category
Amino Acids
Molecular Weight
472.6
Molecular Formula
C21H36N4O6S

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Specification

Synonyms
N-alpha-Boc-N-epsilon-Biotinyl-L-lysine, Boc-Lys(Biotinyl), Boc-Lys(Biotin)-OH
Canonical SMILES
[H][C@]12CS[C@@H](CCCCC(=O)NCCCC[C@H](NC(=O)OC(C)(C)C)C(O)=O)[C@@]1([H])NC(=O)N2
InChI
1S/C21H36N4O6S/c1-21(2,3)31-20(30)24-13(18(27)28)8-6-7-11-22-16(26)10-5-4-9-15-17-14(12-32-15)23-19(29)25-17/h13-15,17H,4-12H2,1-3H3,(H,22,26)(H,24,30)(H,27,28)(H2,23,25,29)/t13-,14-,15-,17-/m0/s1
InChI Key
XTQNFOCBPUXJCS-JKQORVJESA-N
Application
Peptide synthesis.
Assay
≥98.0% (TLC)
Beilstein
5797526
Functional Group
Boc
MDL Number
MFCD00133628
NACRES
NA.22
PubChem ID
57647301
Storage Temperature
4 ℃
Type
Standard Amino Acids, Dye Labeled, Lysine (Lys)
WGK Germany
3

Upstream Synthesis Route 1

  • 13734-28-6
  • 33755-53-2
  • 62062-43-5

Reference: [1]Bodanszky,M.; Fagan,D.T.
[Journal of the American Chemical Society, 1977, vol. 99, # 1, p. 235 - 239]

Downstream Synthesis Route 1

  • 62062-43-5
  • 576-19-2

Reference: [1] Journal of the American Chemical Society, 1977, vol. 99, # 1, p. 235 - 239

Downstream Synthesis Route 2

  • 62062-43-5
  • 576-19-2

Reference: [1]Journal of the American Chemical Society,1977,vol. 99,p. 235 - 239

Downstream Synthesis Route 3

  • 51-67-2
  • 62062-43-5
  • 168639-61-0

Reference: [1]Finn, Frances M.; Yamanouchi, Keitaro; Titus, Gail; Hofmann, Klaus
[Bioorganic Chemistry, 1995, vol. 23, # 2, p. 152 - 168]

* For details of the synthesis route, please refer to the original source to ensure accuracy.

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