Boc-L-Orn(Boc)-OH - ≥98% , CAS No.57133-29-6

CAS: 57133-29-6 Cat. No.: B356835 Peso molecular: 332.4

GRADE & PURITY ≥98%

Synonyms

Nalpha,Ndelta-bis-Boc-ornithine | O11703 | Di-N-(tert-butoxycarbonyl)-L-ornithine | N,N'-bis-BOC-ornithine | Boc-Orn(Boc) | N2,N5-Di-Boc-L-ornithine | N2,N5-bis(tert-butoxycarbonyl)-L-ornithine | CCG-202852 | DS-14736 | N,N'-Di(Boc)-L-ornithine | N-alpha-

Storage

Store at 2-8°C

Shipped In

Wet ice

Specifications

Sinónimos

Nalpha, Ndelta-bis-Boc-ornithine | O11703 | Di-N-(tert-butoxycarbonyl)-L-ornithine | N, N'-bis-BOC-ornithine | Boc-Orn(Boc) | N2, N5-Di-Boc-L-ornithine | N2, N5-bis(tert-butoxycarbonyl)-L-ornithine | CCG-202852 | DS-14736 | N, N'-Di(Boc)-L-ornithine | N-alpha-

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C

Enviado en

Wet ice

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 504764544
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504764544
• Sonrisas canónicas: CC(C)(C)OC(=O)NCCCC(C(=O)O)NC(=O)OC(C)(C)C
• IUPAC Name: (2S)-2,5-bis[(2-methylpropan-2-yl)oxycarbonylamino]pentanoic acid
• InChIKey: RJOJSMIZZYHNQG-JTQLQIEISA-N
• INCHI: 1S/C15H28N2O6/c1-14(2,3)22-12(20)16-9-7-8-10(11(18)19)17-13(21)23-15(4,5)6/h10H,7-9H2,1-6H3,(H,16,20)(H,17,21)(H,18,19)/t10-/m0/s1
• Isómeros SMILES: CC(C)(C)OC(=O)NCCC[C@@H](C(=O)O)NC(=O)OC(C)(C)C
• Peso molecular: 332.4
• Reaxy-Rn: 21156764
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=21156764&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Carboxylic acids and derivatives
      • Subclass Amino acids, peptides, and analogues
        • Level5 Amino acids and derivatives
          • Level6 Alpha amino acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Carboxylic acids and derivatives
• Subclass: Amino acids, peptides, and analogues
• Intermediate Tree Nodes: Amino acids and derivatives
• Direct Parent: Alpha amino acids and derivatives
• Alternative Parents: Branched fatty acids Carbamate esters Monocarboxylic acids and derivatives Carboxylic acids Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Alpha-amino acid or derivatives - Branched fatty acid - Fatty acyl - Fatty acid - Carbamic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as alpha amino acids and derivatives. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof.
• 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

Propiedades químicas y físicas

• Peso molecular: 332.390 g/mol
• XLogP3: 2.000
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 10
• Exact Mass: 332.195 Da
• Monoisotopic Mass: 332.195 Da
• Topological Polar Surface Area: 114.000 Ų
• Heavy Atom Count: 23
• Formal Charge: 0
• Complexity: 423.000
• 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

Referencias

1. Tsogzolmaa Ganbold, Qingming Bao, Hai Xiao, Dolgorsuren Zurgaanjin, Caifeng Liu, Shuqin Han, Agula Hasi, Huricha Baigude.  (2022)  Peptidomimetic Lipid-Nanoparticle-Mediated Knockdown of TLR4 in CNS Protects against Cerebral Ischemia/Reperfusion Injury in Mice.  Nanomaterials,  12  (12): (2072).  [PMID:35745411] [10.3390/nano12122072]

2. Gerile Gerile, Tsogzolmaa Ganbold, Yizheng Li, Huricha Baigude.  (2017)  Head group configuration increases the biocompatibility of cationic lipids for nucleic acid delivery.  Journal of Materials Chemistry B,  5  (28): (5597-5607).  [PMID:] [10.1039/C7TB00317J]