2-Amino-1-phenylethanol - 10mM in DMSO , CAS No.7568-93-6

CAS: 7568-93-6 Cat. No.: A425852 Peso molecular: 137.18 Beilstein Registry Number: 971222 Número EC: 231-469-1

GRADE & PURITY 10mM in DMSO

Synonyms

(RS)-2-Amino-1-phenylethanol | Benzenemethanol, alpha-(aminomethyl)- (VAN) | beta-Hydroxy-beta-phenylethylamine | beta-hydroxy-beta-phenyl-Ethylamine | BRN 0971222 | Oprea1_790333 | (+-)-Phenylethanolamine | NSC5021 | NSC-5021 | Phenylethanolamin | (1R)-2

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Specifications

Sinónimos

(RS)-2-Amino-1-phenylethanol | Benzenemethanol, alpha-(aminomethyl)- (VAN) | beta-Hydroxy-beta-phenylethylamine | beta-hydroxy-beta-phenyl-Ethylamine | BRN 0971222 | Oprea1_790333 | (+-)-Phenylethanolamine | NSC5021 | NSC-5021 | Phenylethanolamin | (1R)-2

Especificaciones y pureza

10mM in DMSO

Condiciones de almacenamiento de almacenamiento

Store at -80°C

Enviado en

Dry ice packs + Cold packs

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Nombres e identificadores

• Sonrisas canónicas: C1=CC=C(C=C1)C(CN)O
• IUPAC Name: 2-amino-1-phenylethanol
• InChIKey: ULSIYEODSMZIPX-UHFFFAOYSA-N
• INCHI: 1S/C8H11NO/c9-6-8(10)7-4-2-1-3-5-7/h1-5,8,10H,6,9H2
• Isómeros SMILES: C1=CC=C(C=C1)C(CN)O
• WGK Alemania: 3
• RTECS: DN5500000
• Peso molecular: 137.18
• Beilstein: 971222
• Reaxy-Rn: 971222
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=971222&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Clase Organonitrogen compounds
      • Subclass Amines

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Clase: Organonitrogen compounds
• Subclass: Amines
• Intermediate Tree Nodes: Not available
• Direct Parent: Aralkylamines
• Alternative Parents: Benzene and substituted derivatives Secondary alcohols 1,2-aminoalcohols Organopnictogen compounds Monoalkylamines Hydrocarbon derivatives Aromatic alcohols
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Aralkylamine - Benzenoid - Monocyclic benzene moiety - Secondary alcohol - 1,2-aminoalcohol - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Aromatic alcohol - Primary amine - Organooxygen compound - Primary aliphatic amine - Alcohol - Aromatic homomonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as aralkylamines. These are alkylamines in which the alkyl group is substituted at one carbon atom by an aromatic hydrocarbyl group.
• External Descriptors: phenylethanolamines

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

Mecanismos de acción

Propiedades químicas y físicas

• Sensibilidad: air sensitive
• Punto de fusión (°C): 57 °C
• Peso molecular: 137.180 g/mol
• XLogP3: 0.100
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 137.084 Da
• Monoisotopic Mass: 137.084 Da
• Topological Polar Surface Area: 46.300 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 89.300
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 1
• 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. Shen Yong, Bai Xue, Wang Jiaxi, Zhou Xiran, Meng Rizeng, Guo Na.  (2023)  Inhibitory Effect of Non-Saccharomyces Starmerella bacillaris CC-PT4 Isolated from Grape on MRSA Growth and Biofilm.  Probiotics and Antimicrobial Proteins,      [PMID:37639210] [10.1007/s12602-023-10146-7]

2. Yongzhan Mai, Songyao Peng, Haiyan Li, Zini Lai.  (2019)  Histological, biochemical and transcriptomic analyses reveal liver damage in zebrafish (Danio rerio) exposed to phenanthrene.  COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-TOXICOLOGY & PHARMACOLOGY,      [PMID:31374294] [10.1016/j.cbpc.2019.108582]