Z-Lys(Z)-OH - ≥98% , CAS No.405-39-0

CAS: 405-39-0 Cat. No.: Z113947 Molecular Weight: 414.45 Beilstein Registry Number: 1897206 EC Number: 206-971-9

GRADE & PURITY ≥98%

Synonyms

Z-Lys(Z)-OH, >=98.0% (TLC) | (S)-2,6-bis(benzyloxycarbonylamino)hexanoic acid | Q-101776 | DTXSID001260463 | (2S)-2,6-bis(phenylmethoxycarbonylamino)hexanoic acid | Z-Lys (Z)-OH | N(alpha),N(epsilon)-di-Z-L-lysine | Z-L-Lys(Z)-OH | BBL038146 | AKOS0159241

Storage

Room temperature

Shipped In

Normal

Specifications

Synonyms

Z-Lys(Z)-OH, >=98.0% (TLC) | (S)-2, 6-bis(benzyloxycarbonylamino)hexanoic acid | Q-101776 | DTXSID001260463 | (2S)-2, 6-bis(phenylmethoxycarbonylamino)hexanoic acid | Z-Lys (Z)-OH | N(alpha), N(epsilon)-di-Z-L-lysine | Z-L-Lys(Z)-OH | BBL038146 | AKOS0159241

Specifications & Purity

≥98%

Storage

Room temperature

Shipped In

Normal

Purity

≥98%

Names and Identifiers

• Pubchem Sid: 488196228
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488196228
• Canonical Smiles: C1=CC=C(C=C1)COC(=O)NCCCCC(C(=O)O)NC(=O)OCC2=CC=CC=C2
• IUPAC Name: (2S)-2,6-bis(phenylmethoxycarbonylamino)hexanoic acid
• InChIKey: BLZXFNUZFTZCFD-IBGZPJMESA-N
• INCHI: 1S/C22H26N2O6/c25-20(26)19(24-22(28)30-16-18-11-5-2-6-12-18)13-7-8-14-23-21(27)29-15-17-9-3-1-4-10-17/h1-6,9-12,19H,7-8,13-16H2,(H,23,27)(H,24,28)(H,25,26)/t19-/m0/s1
• Isomeric SMILES: C1=CC=C(C=C1)COC(=O)NCCCC[C@@H](C(=O)O)NC(=O)OCC2=CC=CC=C2
• WGK Germany: 3
• Molecular Weight: 414.45
• Beilstein: 1897206
• Reaxy-Rn: 2027663
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2027663&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Class Benzene and substituted derivatives
      • Subclass Benzyloxycarbonyls

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Class: Benzene and substituted derivatives
• Subclass: Benzyloxycarbonyls
• Intermediate Tree Nodes: Not available
• Direct Parent: Benzyloxycarbonyls
• Alternative Parents: Alpha amino acids and derivatives Medium-chain fatty acids Amino fatty acids Carbamate esters Monocarboxylic acids and derivatives Carboxylic acids Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Alpha-amino acid or derivatives - Benzyloxycarbonyl - Medium-chain fatty acid - Amino fatty acid - Fatty acyl - Fatty acid - Carbamic acid ester - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organic oxygen compound - Aromatic homomonocyclic compound
• Description: This compound belongs to the class of organic compounds known as benzyloxycarbonyls. These are organic compounds containing a carbonyl group substituted with a benzyloxyl group.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Mechanisms of Action

Chemical and Physical Properties

• Molecular Weight: 414.500 g/mol
• XLogP3: 3.400
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 13
• Exact Mass: 414.179 Da
• Monoisotopic Mass: 414.179 Da
• Topological Polar Surface Area: 114.000 Ų
• Heavy Atom Count: 30
• Formal Charge: 0
• Complexity: 530.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 1
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

References

1. Jian Sun, Jintao Ye, Wenwei Tang, Bin Yu, Yong Gao, Shengli Wang, Haijuan Zhang.  (2025)  A redox-responsive NIR fluorescent nanoprobe for tumor microenvironment-activated surgical navigation with submillimeter precision.  Journal of Materials Chemistry B,      [PMID:40711756] [10.1039/D5TB01157D]