D-Valinol - ≥98% , CAS No.4276-09-9

CAS: 4276-09-9 Cat. No.: V118431 Formula: C₅H₁₃NO Peso molecolare: 103.16 Beilstein Registry Number: 1719138 Numero EC: 922-908-4 PubChem CID: 6950587

GRADE & PURITY ≥98%

Synonyms

(2R)-2-amino-3-methyl-1-butanol | EN300-98065 | (-)-2-amino-3-methyl-1-butanol | AS-12364 | Q-200023 | (2R)-2-amino-3-methylbutan-1-ol | HY-30167 | (R)-valinol | 1-Butanol, 2-amino-3-methyl-, (2R)- | Valinol, D- | (1R)-1-Isopropyl-2-hydroxyethylamine | (R

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Specifications

Sinonimi

(2R)-2-amino-3-methyl-1-butanol | EN300-98065 | (-)-2-amino-3-methyl-1-butanol | AS-12364 | Q-200023 | (2R)-2-amino-3-methylbutan-1-ol | HY-30167 | (R)-valinol | 1-Butanol, 2-amino-3-methyl-, (2R)- | Valinol, D- | (1R)-1-Isopropyl-2-hydroxyethylamine | (R

Specifiche e purezza

≥98%

Condizioni di conservazione di stoccaggio

Store at 2-8°C,Argon charged

Spedito in

Wet ice

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Purezza

≥98%

Nomi e identificatori

• Pubchem Sid: 488195904
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488195904
• Sorrisi canonici: CC(C)C(CO)N
• IUPAC Name: (2R)-2-amino-3-methylbutan-1-ol
• InChIKey: NWYYWIJOWOLJNR-YFKPBYRVSA-N
• INCHI: 1S/C5H13NO/c1-4(2)5(6)3-7/h4-5,7H,3,6H2,1-2H3/t5-/m0/s1
• Isomeri SMILES: CC(C)[C@H](CO)N
• WGK Germania: 3
• PubChem CID: 6950587
• Peso molecolare: 103.16
• Beilstein: 1719138
• Reaxy-Rn: 1719138

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Classe: Organonitrogen compounds
• Subclass: Amines
• Intermediate Tree Nodes: Alkanolamines
• Direct Parent: 1,2-aminoalcohols
• Alternative Parents: Primary alcohols Monoalkylamines Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: 1,2-aminoalcohol - Organic oxygen compound - Hydrocarbon derivative - Primary amine - Primary alcohol - Organooxygen compound - Primary aliphatic amine - Alcohol - Aliphatic acyclic compound
• Descrizione: 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: 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

Proprietà chimiche e fisiche

• Sensibilità: Air sensitive
• Indice di rifrazione: 1.455
• Rotazione specifica [α]: -18 ° (C=10, EtOH)
• Punto di infiammabilità (°F): 172.4 °F
• Punto di infiammabilità (°C): 78°C
• Punto di ebollizione (°C): 189-190°C
• Punto di fusione (°C): 32-36°C
• Peso molecolare: 103.160 g/mol
• XLogP3: 0.000
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 103.1 Da
• Monoisotopic Mass: 103.1 Da
• Topological Polar Surface Area: 46.300 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 45.300
• 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

Riferimenti

1. Lilan Tan, Wenrong Cai, Fangqin Wang, Junyao Li, Datong Wu, Yong Kong.  (2024)  Postsynthetic Modification Strategy for Constructing Electrochemiluminescence-Active Chiral Covalent Organic Frameworks Performing Efficient Enantioselective Sensing.  ANALYTICAL CHEMISTRY,      [PMID:38394220] [10.1021/acs.analchem.3c05887]