(R)-(-)-1-Amino-2-propanol - ≥98%(GC) , CAS No.2799-16-8

CAS: 2799-16-8 Cat. No.: R160942 Peso molecular: 75.11 Número EC: 220-532-9

GRADE & PURITY ≥98%(GC)

Synonyms

(R)-1-amino 2-propanol | A13190 | AKOS006340931 | 1-Amino-2-propanol # | (2R)-1-amino-2-propanol | A0974 | EINECS 220-532-9 | (R)-1-amino-propan-2-ol | (R)-1-aminopropan-2-ol | (R)-1-Amino-2-propanol | (R)-(-)-1-Amino-2-propanol | DTXSID101318940 | (2R)-1

Storage

Argon charged,Room temperature

Shipped In

Normal

Descripción general

el (R)-(-)-1-amino-2-propanol es un intermediario útil para la investigación que se utiliza en la síntesis de otras pequeñas moléculas bioactivas con aplicaciones farmacéuticas.

Specifications

Sinónimos

(R)-1-amino 2-propanol | A13190 | AKOS006340931 | 1-Amino-2-propanol # | (2R)-1-amino-2-propanol | A0974 | EINECS 220-532-9 | (R)-1-amino-propan-2-ol | (R)-1-aminopropan-2-ol | (R)-1-Amino-2-propanol | (R)-(-)-1-Amino-2-propanol | DTXSID101318940 | (2R)-1

Especificaciones y pureza

≥98%(GC)

Condiciones de almacenamiento de almacenamiento

Argon charged, Room temperature

Enviado en

Normal

Pureza

≥98%(GC)

Nombres e identificadores

• Pubchem Sid: 488189757
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488189757
• Sonrisas canónicas: CC(CN)O
• IUPAC Name: (2R)-1-aminopropan-2-ol
• InChIKey: HXKKHQJGJAFBHI-GSVOUGTGSA-N
• INCHI: 1S/C3H9NO/c1-3(5)2-4/h3,5H,2,4H2,1H3/t3-/m1/s1
• Isómeros SMILES: C[C@H](CN)O
• WGK Alemania: 1
• Peso molecular: 75.11
• Reaxy-Rn: 605275
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=605275&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Clase Organonitrogen compounds
      • Subclass Amines
        • Level5 Alkanolamines
          • Level6 1,2-aminoalcohols

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Clase: Organonitrogen compounds
• Subclass: Amines
• Intermediate Tree Nodes: Alkanolamines
• Direct Parent: 1,2-aminoalcohols
• Alternative Parents: Secondary alcohols Organopnictogen compounds Monoalkylamines Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Secondary alcohol - 1,2-aminoalcohol - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organooxygen compound - Primary aliphatic amine - Alcohol - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as 1,2-aminoalcohols. These are organic compounds containing an alkyl chain with an amine group bound to the C1 atom and an alcohol group bound to the C2 atom.
• External Descriptors: Biogenic amines

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 & light & Air sensitive
• Rotación específica [α]: -24° (C=1,MeOH)
• Punto de inflamación (°F): 159.8 °F
• Punto de inflamación (°C): 71 °C
• Punto de ebullición (°C): 160 °C
• Punto de fusión (°C): 24 °C
• Peso molecular: 75.110 g/mol
• XLogP3: -1.000
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 75.0684 Da
• Monoisotopic Mass: 75.0684 Da
• Topological Polar Surface Area: 46.300 Ų
• Heavy Atom Count: 5
• Formal Charge: 0
• Complexity: 22.900
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 1
• 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. Hai-Min Shen, Hong-Bing Ji.  (2013)  Cyclodextrin–[RuCl2(Arene)]2 conjugates: another way to enhance the enantioselectivity of aromatic ketones reduction by aromatic ligands' volume.  TETRAHEDRON,      [PMID:] [10.1016/j.tet.2013.07.077]

2. Ningbo Yu, Shaofei Wang, Min Zhou, Min Xiao, Bo Jin, Hongxia Gao, Zhiwu Liang.  (2026)  Unveiling solvent encapsulation-driven kinetic inversion in CO2 absorption by water-lean amine solvents.  AICHE JOURNAL,      [PMID:] [10.1002/aic.70260]