CYPMPO - ≥97% , CAS No.934182-09-9

CAS: 934182-09-9 Cat. No.: C354297 Peso molecular: 247.23 Número EC: 635-117-1

GRADE & PURITY ≥97%

Synonyms

5-(2,2-Dimethyl-1,3-propoxy cyclophosphoryl)-5-methyl-1-pyrroline N-oxide | CYPMPO, for ESR-spectroscopy, >=97% | 5,5-dimethyl-2-(2-methyl-1-oxido-3,4-dihydropyrrol-1-ium-2-yl)-1,3,2lambda5-dioxaphosphinane 2-oxide | SCHEMBL464608 | CYPMPO | HY-135152 | 2

Storage

Store at -20°C,Argon charged

Shipped In

Ice chest + Ice pads

Descripción general

CYPMPO is a solvent used in electron spin resonance (ESR) free radical spin trapping. One advantage to using CYPMPO is that it shows preference for trapping superoxide and hydroxyl radicals. Studies indicate that ESR trapping of free radicals is very difficult on lipophilic antioxidants as a result of poor solubility and formation unstable adducts. CYPMPO is favorable because it can form stable adducts that are clearly separated and identifiable in ESR. Furthermore, CYPMPO is efficient in biological and chemical systems because of its low toxicity.

Specifications

Sinónimos

5-(2, 2-Dimethyl-1, 3-propoxy cyclophosphoryl)-5-methyl-1-pyrroline N-oxide | CYPMPO, for ESR-spectroscopy, >=97% | 5, 5-dimethyl-2-(2-methyl-1-oxido-3, 4-dihydropyrrol-1-ium-2-yl)-1, 3, 2lambda5-dioxaphosphinane 2-oxide | SCHEMBL464608 | CYPMPO | HY-135152 | 2

Especificaciones y pureza

≥97%

Condiciones de almacenamiento de almacenamiento

Store at -20°C, Argon charged

Enviado en

Ice chest + Ice pads

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

Pureza

≥97%

Nombres e identificadores

• Sonrisas canónicas: CC1(COP(=O)(OC1)C2(CCC=[N+]2[O-])C)C
• IUPAC Name: 5,5-dimethyl-2-(2-methyl-1-oxido-3,4-dihydropyrrol-1-ium-2-yl)-1,3,2λ5-dioxaphosphinane 2-oxide
• InChIKey: OSKIWEPJAIOTFB-UHFFFAOYSA-N
• INCHI: 1S/C10H18NO4P/c1-9(2)7-14-16(13,15-8-9)10(3)5-4-6-11(10)12/h6H,4-5,7-8H2,1-3H3
• Isómeros SMILES: CC1(COP(=O)(OC1)C2(CCC=[N+]2[O-])C)C
• Peso molecular: 247.23
• Reaxy-Rn: 21360617
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=21360617&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Organic phosphonic acids and derivatives
      • Subclass Phosphonic acid diesters

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Organic phosphonic acids and derivatives
• Subclass: Phosphonic acid diesters
• Intermediate Tree Nodes: Not available
• Direct Parent: Dialkyl alkylphosphonates
• Alternative Parents: Phosphonic acid esters Pyrrolines Nitrones Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Azacyclic compounds Organophosphorus compounds Organooxygen compounds Organonitrogen compounds Organic salts Organic oxides Hydrocarbon derivatives Organic cations
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Dialkyl alkylphosphonate - Phosphonic acid ester - Pyrroline - Nitrone - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organoheterocyclic compound - Azacycle - Oxacycle - Organic nitrogen compound - Organic oxide - Organonitrogen compound - Organic salt - Organooxygen compound - Organophosphorus compound - Organic oxygen compound - Hydrocarbon derivative - Organic cation - Aliphatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as dialkyl alkylphosphonates. These are compounds containing a phosphonic acid that is diesterified with alkyl groups, and the phosphorus atom is also directly attached to an alkyl group.
• 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

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Soluble in water (10mg/ml) at 25°C
• Sensibilidad: Moisture sensitive
• Punto de fusión (°C): 126° C
• Peso molecular: 247.230 g/mol
• XLogP3: -0.300
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 1
• Exact Mass: 247.097 Da
• Monoisotopic Mass: 247.097 Da
• Topological Polar Surface Area: 64.300 Ų
• Heavy Atom Count: 16
• Formal Charge: 0
• Complexity: 365.000
• 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. Zhang Yingying, Wu Yingnan, Jing Zehao, Chen Xiaoqiang, Li Mingle, Peng Xiaojun.  (2026)  Preparation of ENBSe-based photoredox catalysts for O2-independent phototherapy in living systems.  Nature Protocols,      [PMID:] [10.1038/s41596-025-01328-4]