3-Aminophenol - ≥98% , CAS No.591-27-5

CAS: 591-27-5 Cat. No.: A108481 Fórmula: C₆H₇NO Peso molecular: 109.13 Beilstein Registry Number: 636059 Número CE: 209-711-2

GRAU & PUREZA ≥98%

Synonyms

Fourrine EG|Tertral EG|Pelagol EG|M-AMINOPHENOL|3-Hydroxyaniline|3-Amino-1-hydroxybenzene|m-Hydroxyaniline|1-Amino-3-hydroxybenzene|Phenol, 3-amino-|Ursol EG|Furro EG|Futramine EG|Renal EG|3-Aminophenol|3-amino-phenol|Fouramine EG|m-Hydroxyaminobenzene

Storage

Protected from light,Room temperature,Argon charged

Shipped In

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Visão geral

3-Aminophenol has been used in the synthesis of disulfonated bis[4-(3-aminophenoxy)phenyl]sulfone (S-BAPS).
It can be used to synthesize:
Methyl 2-oxo-7-[(triphenylphosphoranylidene)amino]-2H-chromene-4-carboxylate by reacting with dimethyl acetylenedicarboxylate (DMAD) in the presence of triphenylphosphine.
3-Amino-2-cyclohexen-1-one via palladium-catalyzed hydrogenation.

Especificações

Sinónimos

Fourrine EG | Tertral EG | Pelagol EG | M-AMINOPHENOL | 3-Hydroxyaniline | 3-Amino-1-hydroxybenzene | m-Hydroxyaniline | 1-Amino-3-hydroxybenzene | Phenol, 3-amino- | Ursol EG | Furro EG | Futramine EG | Renal EG | 3-Aminophenol | 3-amino-phenol | Fouramine EG | m-Hydroxyaminobenzene

Especificações e pureza

≥98%

Condições de armazenamento de armazenamento

Protected from light,Room temperature,Argon charged

Enviado em

FedEx DG Service

Pureza

≥98%

Nomes e identificadores

Pubchem Sid

488181383

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488181383

Sorrisos canónicos

C1=CC(=CC(=C1)O)N

IUPAC Name

3-aminophenol

InChIKey

CWLKGDAVCFYWJK-UHFFFAOYSA-N

INCHI

1S/C6H7NO/c7-5-2-1-3-6(8)4-5/h1-4,8H,7H2

SMILES isoméricas

C1=CC(=CC(=C1)O)N

WGK Alemanha

2

RTECS

SJ4900000

Número UN

2512

Grupo de embalagem

III

Peso molecular

109.13

Beilstein

636059

Reaxy-Rn

636059

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=636059&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Benzene and substituted derivatives
      • Subclass Aniline and substituted anilines

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Benzene and substituted derivatives
• Subclass: Aniline and substituted anilines
• Intermediate Tree Nodes: Not available
• Direct Parent: Aniline and substituted anilines
• Alternative Parents: m-Aminophenols 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Primary amines Organopnictogen compounds Organooxygen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: M-aminophenol - Aniline or substituted anilines - Aminophenol - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Amine - Aromatic homomonocyclic compound
• Descrição: This compound belongs to the class of organic compounds known as aniline and substituted anilines. These are organic compounds containing an aminobenzene moiety.
• External Descriptors: aminophenol

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

Alvos associados (humanos)

CA2 Tclin Carbonic anhydrase II (17698 Activities)

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CA1 Tclin Carbonic anhydrase I (13240 Activities)

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CA14 Tclin Carbonic anhydrase XIV (1305 Activities)

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ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)

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NR1H4 Tclin Bile acid receptor FXR (6228 Activities)

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CA12 Tclin Carbonic anhydrase XII (6231 Activities)

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CA9 Tclin Carbonic anhydrase IX (8255 Activities)

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TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)

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GMNN Tbio Geminin (128009 Activities)

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USP1 Tchem Ubiquitin carboxyl-terminal hydrolase 1 (22556 Activities)

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RUNX1 Tbio Runt-related transcription factor 1/Core-binding factor subunit beta (7867 Activities)

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Alvos associados (não humanos)

Ca7 Carbonic anhydrase VII (3 Activities)

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Bacillus subtilis (32866 Activities)

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Plasmodium falciparum (966862 Activities)

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Poliovirus 1 (1274 Activities)

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L1210 (27553 Activities)

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Txnrd1 Thioredoxin reductase 1, cytoplasmic (45279 Activities)

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TGR Thioredoxin glutathione reductase (28579 Activities)

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Rorc Nuclear receptor ROR-gamma (89407 Activities)

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Mecanismos de ação

Propriedades químicas e físicas

• Solubilidade: Soluble in water (35 mg/ml at 20°C), ether, alcohol, amyl alcohol, and benzene (slightly).
• Sensibilidade: air sensitive ;light sensitive
• Ponto de inflamação (°C): 155℃
• Ponto de ebulição (°C): 164 °C/11 mmHg
• Ponto de fusão (°C): 123℃
• Peso molecular: 109.130 g/mol
• XLogP3: 0.200
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 109.053 Da
• Monoisotopic Mass: 109.053 Da
• Topological Polar Surface Area: 46.300 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 74.900
• 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: 1