Formic Acid - Triethylamine (5:2) Azeotrope - ≥98% , CAS No.15077-13-1

CAS: 15077-13-1 Cat. No.: F302957 Peso molecular: 86.5 Número EC: 683-385-3

GRADE & PURITY ≥98%

Synonyms

N,N-diethylethanamine;formic acid | D90698 | AKOS028109881 | Formic Acid - Triethylamine (5:2) Azeotrope | F1202 | FT-0731198 | Triethylammonium formate 2:5 | Formic acid--N,N-diethylethanamine (5/2) | J-008740 | MFCD00040600 | bis(triethylamine) pentafor

Storage

Room temperature,Argon charged,Desiccated

Shipped In

Normal

Descripción general

application：

Reductant for iridium-catalyzed greener amine synthesis by transfer hydrogenation of imines.

Specifications

Sinónimos

N, N-diethylethanamine;formic acid | D90698 | AKOS028109881 | Formic Acid - Triethylamine (5:2) Azeotrope | F1202 | FT-0731198 | Triethylammonium formate 2:5 | Formic acid--N, N-diethylethanamine (5/2) | J-008740 | MFCD00040600 | bis(triethylamine) pentafor

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Room temperature, Argon charged, Desiccated

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 488199076
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488199076
• Sonrisas canónicas: CCN(CC)CC.CCN(CC)CC.C(=O)O.C(=O)O.C(=O)O.C(=O)O.C(=O)O
• IUPAC Name: N,N-diethylethanamine;formic acid
• InChIKey: NLOIHFJXBNFDSF-UHFFFAOYSA-N
• INCHI: 1S/2C6H15N.5CH2O2/c2*1-4-7(5-2)6-3;5*2-1-3/h2*4-6H2,1-3H3;5*1H,(H,2,3)
• Isómeros SMILES: CCN(CC)CC.CCN(CC)CC.C(=O)O.C(=O)O.C(=O)O.C(=O)O.C(=O)O
• Peso molecular: 86.5
• Reaxy-Rn: 13662216
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=13662216&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Carboxylic acids and derivatives
      • Subclass Carboxylic acids

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Carboxylic acids and derivatives
• Subclass: Carboxylic acids
• Intermediate Tree Nodes: Not available
• Direct Parent: Carboxylic acids
• Alternative Parents: Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Not available
• Substituents: Monocarboxylic acid or derivatives - Carboxylic acid - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as carboxylic acids. These are compounds containing a carboxylic acid group with the formula -C(=O)OH.
• 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: Moisture sensitive.
• Índice de refracción: 1.43
• Punto de inflamación (°C): 110 °C
• Punto de ebullición (°C): 194 °C
• Punto de fusión (°C): 15 °C
• Peso molecular: 432.500 g/mol
• Hydrogen Bond Donor Count: 5
• Hydrogen Bond Acceptor Count: 12
• Rotatable Bond Count: 6
• Exact Mass: 432.268 Da
• Monoisotopic Mass: 432.268 Da
• Topological Polar Surface Area: 193.000 Ų
• Heavy Atom Count: 29
• Formal Charge: 0
• Complexity: 35.900
• 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: 7

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