GRADE & PURITY ≥99%

Synonyms

AKOS000120988 | Isopropylaniline | UNII-I7Y9616F3R | SCHEMBL66892 | D70367 | Aniline, N-isopropyl- | A838867 | GS-3034 | MFCD00026347 | AC-14912 | I7Y9616F3R | DTXSID7025479 | N-ISOPROPYLANILINE | N-iso-Propylaniline | n-isopropyl-aniline | CCRIS 4831 | I

Storage

Argon charged,Room temperature

Shipped In

Normal

Descripción general

General description：

N-Isopropylaniline is an intermediate in propachlor degradation.

application：

N-Isopropylaniline has been used to study the mechanism of metabolism of propachlor by Pseudomonas sp.strain PEM1.

Specifications

Sinónimos

AKOS000120988 | Isopropylaniline | UNII-I7Y9616F3R | SCHEMBL66892 | D70367 | Aniline, N-isopropyl- | A838867 | GS-3034 | MFCD00026347 | AC-14912 | I7Y9616F3R | DTXSID7025479 | N-ISOPROPYLANILINE | N-iso-Propylaniline | n-isopropyl-aniline | CCRIS 4831 | I

Especificaciones y pureza

≥99%

Condiciones de almacenamiento de almacenamiento

Argon charged, Room temperature

Enviado en

Normal

Pureza

≥99%

Nombres e identificadores

• Pubchem Sid: 488181774
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488181774
• Sonrisas canónicas: CC(C)NC1=CC=CC=C1
• IUPAC Name: N-propan-2-ylaniline
• InChIKey: FRCFWPVMFJMNDP-UHFFFAOYSA-N
• INCHI: 1S/C9H13N/c1-8(2)10-9-6-4-3-5-7-9/h3-8,10H,1-2H3
• Isómeros SMILES: CC(C)NC1=CC=CC=C1
• WGK Alemania: 3
• RTECS: BY4190000
• Número ONU: 2810
• Grupo de embalaje: I
• Peso molecular: 135.21
• Beilstein: 2205870
• Reaxy-Rn: 2205871
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2205871&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Clase Organonitrogen compounds
      • Subclass Amines
        • Level5 Aralkylamines
          • Level6 Phenylalkylamines
            • Level7 Phenylisopropylamines

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Clase: Organonitrogen compounds
• Subclass: Amines
• Intermediate Tree Nodes: Aralkylamines - Phenylalkylamines
• Direct Parent: Phenylisopropylamines
• Alternative Parents: Aniline and substituted anilines Secondary alkylarylamines Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Phenylisopropylamine - Aniline or substituted anilines - Secondary aliphatic/aromatic amine - Benzenoid - Monocyclic benzene moiety - Secondary amine - Organopnictogen compound - Hydrocarbon derivative - Aromatic homomonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as phenylisopropylamines. These are organic aromatic compounds containing a 1-phenylpropan-2-amine moiety.
• 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

Objetivos asociados (humanos)

POLI Tchem DNA polymerase iota (116820 Activities)

Discover Target: POLI

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)

Discover Target: TDP1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ERG Tbio Transcriptional regulator ERG (5589 Activities)

Discover Target: ERG

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Objetivos asociados (no humanos)

Plasmodium falciparum (966862 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

lef Anthrax lethal factor (7585 Activities)

Discover Target: lef

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

pfk 6-phospho-1-fructokinase (7870 Activities)

Discover Target: pfk

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TGR Thioredoxin glutathione reductase (28579 Activities)

Discover Target: TGR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: (Soluble): acetone, alcohol, ether, benzene
• Sensibilidad: Air Sensitive
• Índice de refracción: 1.54
• Punto de inflamación (°F): 179.6 °F
• Punto de inflamación (°C): 88 °C
• Punto de ebullición (°C): 213°C
• Punto de fusión (°C): -50 °C
• Peso molecular: 135.210 g/mol
• XLogP3: 2.500
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• Exact Mass: 135.105 Da
• Monoisotopic Mass: 135.105 Da
• Topological Polar Surface Area: 12.000 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 82.700
• 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

1. Ming-Hui He, Mei-Lin Su, Zhao-Hui Yu, Guang-Xue Chen, Zhao-Hua Zeng, Jian-Wen Yang.  (2014)  Benzoylformamides as new photocaged bases for photo-latent anion polymerization.  CHINESE CHEMICAL LETTERS,      [PMID:] [10.1016/j.cclet.2014.10.002]