N-Succinimidyl 5-Azido-2-nitrobenzoate - ≥97% , CAS No.60117-35-3

CAS: 60117-35-3 Cat. No.: N159713 Peso molecular: 305.21 Número EC: 691-356-1

GRADE & PURITY ≥97%

Synonyms

N-5-Azido-2-nitrobenzoyloxysuccinimide | S0860 | 5-Azido-2-nitrobenzoic Acid N-Succinimidyl Ester | Anb-nos | ANB-NOS Crosslinker | N-Succinimidyl 5-Azido-2-nitrobenzoate | 2,5-Pyrrolidinedione, 1-((5-azido-2-nitrobenzoyl)oxy)- | AKOS040741146 | 5-Azido-2

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Descripción general

Product Application:

Photoactive, heterobifunctional cross-linking reagent. Typically, initial reaction couples via ester to primary amine by amide bond formation in the pH range 6.5-8.5. Second bonding occurs during UV irradiation (250-350 nm) via reactive nitrene. The latter bonding is rapid and non-specific.

Specifications

Sinónimos

N-5-Azido-2-nitrobenzoyloxysuccinimide | S0860 | 5-Azido-2-nitrobenzoic Acid N-Succinimidyl Ester | Anb-nos | ANB-NOS Crosslinker | N-Succinimidyl 5-Azido-2-nitrobenzoate | 2, 5-Pyrrolidinedione, 1-((5-azido-2-nitrobenzoyl)oxy)- | AKOS040741146 | 5-Azido-2

Especificaciones y pureza

≥97%

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C, Argon charged

Enviado en

Wet ice

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

Pureza

≥97%

Nombres e identificadores

• Pubchem Sid: 504762393
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504762393
• Sonrisas canónicas: C1CC(=O)N(C1=O)OC(=O)C2=C(C=CC(=C2)N=[N+]=[N-])[N+](=O)[O-]
• IUPAC Name: (2,5-dioxopyrrolidin-1-yl) 5-azido-2-nitrobenzoate
• InChIKey: FUOJEDZPVVDXHI-UHFFFAOYSA-N
• INCHI: 1S/C11H7N5O6/c12-14-13-6-1-2-8(16(20)21)7(5-6)11(19)22-15-9(17)3-4-10(15)18/h1-2,5H,3-4H2
• Isómeros SMILES: C1CC(=O)N(C1=O)OC(=O)C2=C(C=CC(=C2)N=[N+]=[N-])[N+](=O)[O-]
• Peso molecular: 305.21
• Reaxy-Rn: 1173416
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1173416&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Clase Benzene and substituted derivatives
      • Subclass Benzoic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Benzene and substituted derivatives
• Subclass: Benzoic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Nitrobenzoic acids and derivatives
• Alternative Parents: Nitrobenzenes Phenylazides Nitroaromatic compounds Benzoyl derivatives Pyrrolidine-2-ones Dicarboximides Azo compounds Azo imides Lactams Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Organic oxoazanium compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides Organic salts Organic zwitterions
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Nitrobenzoate - Nitrobenzene - Benzoyl - Nitroaromatic compound - Phenylazide - Pyrrolidone - 2-pyrrolidone - Dicarboximide - Pyrrolidine - Azo compound - Azo imide - Lactam - C-nitro compound - Organic nitro compound - Organoheterocyclic compound - Organic 1,3-dipolar compound - Azacycle - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Carboxylic acid derivative - Carbonyl group - Organic oxide - Organic nitrogen compound - Organic oxygen compound - Hydrocarbon derivative - Organic salt - Organic zwitterion - Organonitrogen compound - Organooxygen compound - Aromatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as nitrobenzoic acids and derivatives. These are compounds containing a nitrobenzoic acid moiety, which consists of a benzene ring bearing both a carboxylic acid group and a nitro group on two different ring carbon atoms.
• 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

• Sensibilidad: Light Sensitive,Moisture Sensitive,Heat Sensitive
• Punto de fusión (°C): 136 °C
• Peso molecular: 305.200 g/mol
• XLogP3: 1.700
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 8
• Rotatable Bond Count: 4
• Exact Mass: 305.04 Da
• Monoisotopic Mass: 305.04 Da
• Topological Polar Surface Area: 124.000 Ų
• Heavy Atom Count: 22
• Formal Charge: 0
• Complexity: 550.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• 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