Fosforodicloridato de metilo - ≥95%, used for Methyl dichlorophosphate was used in the synthesis of: 1.4,6-cyclic phosphate tetrasaccharide. 2.8-(2′′-hydroxyethoxy)adenosine-5′,2′′-phosphate derivative. 3.analogs of (R)-1-O-hexadecyl-2-palmitoyl-sn-glycer

CAS: 677-24-7 Cat. No.: M157887 Fórmula: CH₃Cl₂O₂P Peso molecular: 148.91 Beilstein Registry Number: 1286 Número CE: 211-639-1

GRADE & PURITY ≥95%

Synonyms

Methyl dichlorophosphate | UNII-P5R9XZ7EJU | AKOS015856796 | DTXSID50217984 | Methyl phosphorodichloridate | Phosphorodichloridic acid, methyl ester | EINECS 211-639-1 | P5R9XZ7EJU | M0904 | Methyl dichloridophosphate # | phosphoric acid monomethyl ester

Storage

Armazenar a 2-8°C, carregado com árgon

Shipped In

Gelo húmido

Specifications

Sinónimos

Methyl dichlorophosphate | UNII-P5R9XZ7EJU | AKOS015856796 | DTXSID50217984 | Methyl phosphorodichloridate | Phosphorodichloridic acid, methyl ester | EINECS 211-639-1 | P5R9XZ7EJU | M0904 | Methyl dichloridophosphate # | phosphoric acid monomethyl ester

Especificações e pureza

≥95%

Aplicação

Methyl dichlorophosphate was used in the synthesis of: 1.4,6-cyclic phosphate tetrasaccharide. 2.8-(2′′-hydroxyethoxy)adenosine-5′,2′′-phosphate derivative. 3.analogs of (R)-1-O-hexadecyl-2-palmitoyl-sn-glycero-3-phosphoethanolamine poly(ethylene glycol).

Condições de armazenamento de armazenamento

Armazenar a 2-8°C, carregado com árgon

Enviado em

Gelo húmido

Pureza

≥95%

Nomes e identificadores

• Pubchem Sid: 528769671
• Sorrisos canónicos: COP(=O)(Cl)Cl
• IUPAC Name: dichlorophosphoryloxymethane
• InChIKey: SNVCRNWSNUUGEA-UHFFFAOYSA-N
• INCHI: 1S/CH3Cl2O2P/c1-5-6(2,3)4/h1H3
• SMILES isoméricas: COP(=O)(Cl)Cl
• Peso molecular: 148.91
• Beilstein: 1286
• Reaxy-Rn: 969710
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=969710&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Classe Organic phosphoric acids and derivatives
      • Subclass Phosphate esters

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: Organic phosphoric acids and derivatives
• Subclass: Phosphate esters
• Intermediate Tree Nodes: Not available
• Direct Parent: Phosphate esters
• Alternative Parents: Organooxygen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Phosphoric acid ester - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aliphatic acyclic compound
• Descrição: This compound belongs to the class of organic compounds known as phosphate esters. These are organic compounds containing phosphoric acid ester functional group, with the general structure R1P(=O)(R2)OR3. R1,R2 = O,N, or halogen atom; R3 = organyl 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

Propriedades químicas e físicas

• Sensibilidade: Moisture Sensitive；Air Sensitive
• Índice de refração: 1.44
• Ponto de ebulição (°C): 63°C/15mmHg
• Peso molecular: 148.910 g/mol
• XLogP3: 1.000
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 147.925 Da
• Monoisotopic Mass: 147.925 Da
• Topological Polar Surface Area: 26.300 Ų
• Heavy Atom Count: 6
• Formal Charge: 0
• Complexity: 75.600
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• 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