laurato de 4-nitrofenilo - ≥98% , CAS No.1956-11-2

CAS: 1956-11-2 Cat. No.: N159738 Peso molecular: 321.42

GRADE & PURITY ≥98%

Synonyms

dodecanoato de 4-nitrofenilo | dodecanoato de (4-nitrofenilo) | laurato de para-nitrofenilo | laurato de 4-nitrofenilo | éster 4-nitrofenílico del ácido dodecanoico | éster 4-nitrofenílico del ácido láurico | laurato de p-nitrofenilo | dodecanoato de p-ni

Storage

Conservar a 2-8°C

Shipped In

Hielo húmedo

Specifications

Sinónimos

dodecanoato de 4-nitrofenilo | dodecanoato de (4-nitrofenilo) | laurato de para-nitrofenilo | laurato de 4-nitrofenilo | éster 4-nitrofenílico del ácido dodecanoico | éster 4-nitrofenílico del ácido láurico | laurato de p-nitrofenilo | dodecanoato de p-ni

Especificaciones y pureza

≥98%

Mecanismos bioquímicos y fisiológicos

el 4-nitrofenil dodecanoato es un derivado del p-nitrofenol éster y sirve como sustrato modelo típico en los ensayos con lipasas.

Condiciones de almacenamiento de almacenamiento

Conservar a 2-8°C

Enviado en

Hielo húmedo

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 504754861
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504754861
• Sonrisas canónicas: CCCCCCCCCCCC(=O)OC1=CC=C(C=C1)[N+](=O)[O-]
• IUPAC Name: (4-nitrophenyl) dodecanoate
• InChIKey: YNGNVZFHHJEZKD-UHFFFAOYSA-N
• INCHI: 1S/C18H27NO4/c1-2-3-4-5-6-7-8-9-10-11-18(20)23-17-14-12-16(13-15-17)19(21)22/h12-15H,2-11H2,1H3
• Isómeros SMILES: CCCCCCCCCCCC(=O)OC1=CC=C(C=C1)[N+](=O)[O-]
• Peso molecular: 321.42
• Reaxy-Rn: 1889084
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1889084&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Clase Phenol esters

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Phenol esters
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Phenol esters
• Alternative Parents: Nitrobenzenes Phenoxy compounds Nitroaromatic compounds Fatty acid esters Carboxylic acid esters Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Monocarboxylic acids and derivatives Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Phenol ester - Nitrobenzene - Phenoxy compound - Nitroaromatic compound - Fatty acid ester - Monocyclic benzene moiety - Fatty acyl - Carboxylic acid ester - C-nitro compound - Organic nitro compound - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Organic oxoazanium - Organic 1,3-dipolar compound - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Carbonyl group - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Organopnictogen compound - Aromatic homomonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as phenol esters. These are aromatic compounds containing a benzene ring substituted by a hydroxyl group and an ester 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

Propiedades químicas y físicas

• Punto de fusión (°C): 45 °C
• Peso molecular: 321.400 g/mol
• XLogP3: 6.700
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 12
• Exact Mass: 321.194 Da
• Monoisotopic Mass: 321.194 Da
• Topological Polar Surface Area: 72.100 Ų
• Heavy Atom Count: 23
• Formal Charge: 0
• Complexity: 332.000
• 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

Referencias

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