(1R)-(+)-(1-Amino-2-methylpropyl)phosphonic acid - ≥98% , CAS No.66254-56-6

CAS: 66254-56-6 Cat. No.: R472570 Molecular Weight: 153.12 EC Number: 633-165-8 PubChem CID: 2734887

GRADE & PURITY ≥98%

Synonyms

1-AMINO-2-METHYL-PROPYLPHOSPHONIC ACID | SCHEMBL2352061 | (R)-(1-amino-2-methylpropyl)phosphonic acid | Phosphonic acid,[(1R)-1-amino-2-methylpropyl]-(9ci) | (r)-1-amino-2-methylpropylphosphonic acid | J550.870C | (R)-(1-amino-2-methylpropyl)phosphonicaci

Storage

Room temperature

Overview

Description

The enantiodiscrimination of (1R)-(+)-(1-amino-2-methylpropyl)phosphonic acid from its enantiomer in the gas-phase can be done using ESI-MS-CID technique. [electrospray ionization-mass spectrometric detection-collision induced dissociation]Serves as an attractive substitute for amino carboxylic acids in biological systems. Exhibits interesting and useful properties as peptide analog, antiviral agent, hapten for the generation of catalytic antibodies, enzyme inhibitors, potent antibiotics, herbicides, and pesticides.

Specifications

Synonyms

1-AMINO-2-METHYL-PROPYLPHOSPHONIC ACID | SCHEMBL2352061 | (R)-(1-amino-2-methylpropyl)phosphonic acid | Phosphonic acid, [(1R)-1-amino-2-methylpropyl]-(9ci) | (r)-1-amino-2-methylpropylphosphonic acid | J550.870C | (R)-(1-amino-2-methylpropyl)phosphonicaci

Specifications & Purity

≥98%

Storage

Room temperature

Purity

≥98%

Names and Identifiers

• Canonical Smiles: CC(C)C(N)P(=O)(O)O
• IUPAC Name: [(1R)-1-amino-2-methylpropyl]phosphonic acid
• InChIKey: DGSLPJDIFKVSIB-SCSAIBSYSA-N
• INCHI: 1S/C4H12NO3P/c1-3(2)4(5)9(6,7)8/h3-4H,5H2,1-2H3,(H2,6,7,8)/t4-/m1/s1
• Isomeric SMILES: CC(C)[C@H](N)P(=O)(O)O
• WGK Germany: 3
• PubChem CID: 2734887
• Molecular Weight: 153.12

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Class Organic phosphonic acids and derivatives
      • Subclass Organic phosphonic acids

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Class: Organic phosphonic acids and derivatives
• Subclass: Organic phosphonic acids
• Intermediate Tree Nodes: Not available
• Direct Parent: Organic phosphonic acids
• Alternative Parents: Organopnictogen compounds Organophosphorus compounds Organic oxides Monoalkylamines Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Organophosphonic acid - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organophosphorus compound - Organonitrogen compound - Primary aliphatic amine - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as organic phosphonic acids. These are organic compounds containing phosphonic acid.
• 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

Chemical and Physical Properties

• Specific Rotation[α]: [α]20/D +1.0°, c = 1 in 1 M NaOH
• Melt Point(°C): 272-277 °C
• Molecular Weight: 153.120 g/mol
• XLogP3: -3.300
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2
• Exact Mass: 153.055 Da
• Monoisotopic Mass: 153.055 Da
• Topological Polar Surface Area: 83.600 Ų
• Heavy Atom Count: 9
• Formal Charge: 0
• Complexity: 130.000
• 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