4-Nitrophenylethylamine Hydrobromide - ≥98% , CAS No.69447-84-3

CAS: 69447-84-3 Cat. No.: N304417 Peso molecular: 247.092 Número EC: 823-709-4

GRADE & PURITY ≥98%

Synonyms

FT-0645166 | 2-(4-nitrophenyl)ethanamine;hydrobromide | SCHEMBL11379599 | BCP14535 | AS-11036 | Benzeneethanamine, 4-nitro-, hydrobromide (1:1) | 4-Nitrophenylethylamine HBr | 4-nitrophenylethyl amine hbr | 2-(4-Nitrophenyl)ethan-1-amine--hydrogen bromide

Storage

Room temperature,Desiccated

Shipped In

Normal

Specifications

Sinónimos

FT-0645166 | 2-(4-nitrophenyl)ethanamine;hydrobromide | SCHEMBL11379599 | BCP14535 | AS-11036 | Benzeneethanamine, 4-nitro-, hydrobromide (1:1) | 4-Nitrophenylethylamine HBr | 4-nitrophenylethyl amine hbr | 2-(4-Nitrophenyl)ethan-1-amine--hydrogen bromide

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Room temperature, Desiccated

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 504769414
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504769414
• Sonrisas canónicas: C1=CC(=CC=C1CCN)[N+](=O)[O-].Br
• IUPAC Name: 2-(4-nitrophenyl)ethanamine;hydrobromide
• InChIKey: IXEDXMYYHOYVRD-UHFFFAOYSA-N
• INCHI: 1S/C8H10N2O2.BrH/c9-6-5-7-1-3-8(4-2-7)10(11)12;/h1-4H,5-6,9H2;1H
• Isómeros SMILES: C1=CC(=CC=C1CCN)[N+](=O)[O-].Br
• Peso molecular: 247.092
• Reaxy-Rn: 3706017
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3706017&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Benzene and substituted derivatives
• Subclass: Nitrobenzenes
• Intermediate Tree Nodes: Not available
• Direct Parent: Nitrobenzenes
• Alternative Parents: Phenethylamines Nitroaromatic compounds 2-arylethylamines Aralkylamines Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Hydrobromides Organic cations
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Nitrobenzene - Phenethylamine - Nitroaromatic compound - 2-arylethylamine - Aralkylamine - C-nitro compound - Organic nitro compound - Organic oxoazanium - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Primary aliphatic amine - Primary amine - Organic oxide - Organonitrogen compound - Amine - Organic oxygen compound - Organic nitrogen compound - Organic salt - Hydrocarbon derivative - Hydrobromide - Organic cation - Aromatic homomonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as nitrobenzenes. These are compounds containing a nitrobenzene moiety, which consists of a benzene ring with a carbon bearing a nitro 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 inflamación (°C): 159.9ºC
• Punto de ebullición (°C): 340.9ºC
• Peso molecular: 247.090 g/mol
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 246 Da
• Monoisotopic Mass: 246 Da
• Topological Polar Surface Area: 71.800 Ų
• Heavy Atom Count: 13
• Formal Charge: 0
• Complexity: 148.000
• 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: 2

XLogP3

Referencias

1. Kun Ge, Lunzhao Yi, Qiyue Wu, Yonghui Li, Hanqiang Zhang, Ying Gu.  (2021)  Detection of Formaldehyde by Surface-Enhanced Raman Spectroscopy Based on PbBiO2Br/Au4Ag4 Nanospheres.  ACS Applied Nano Materials,      [PMID:] [10.1021/acsanm.1c01710]

2. Caiqing Ma, Yu Liu, Jing Wang, Shiwei Wu, Qian Zhang, Peng Song, Lixin Xia.  (2018)  Regulate the coupling reaction of 4-nitrothiophenol to 4,4′-dimercaptoazobenzene by organic alkali.  JOURNAL OF RAMAN SPECTROSCOPY,  49  (8): (1395-1401).  [PMID:] [10.1002/jrs.5381]