Methyl Phosphorodichloridate - ≥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 Formule: CH₃Cl₂O₂P Poids moléculaire: 148.91 Beilstein Registry Number: 1286 Numéro 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

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Specifications

Synonymes

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

Spécifications et pureté

≥95%

Application

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).

Conditions de stockage de stockage

Store at 2-8°C,Argon charged

Expédié en

Wet ice

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Pureté

≥95%

Noms et identifiants

Pubchem Sid

528769671

Sourires canoniques

COP(=O)(Cl)Cl

IUPAC Name

dichlorophosphoryloxymethane

InChIKey

SNVCRNWSNUUGEA-UHFFFAOYSA-N

INCHI

1S/CH3Cl2O2P/c1-5-6(2,3)4/h1H3

Isomères SMILES

COP(=O)(Cl)Cl

Poids moléculaire

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
• Description: 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

Propriétés chimiques et physiques

• Sensibilité: Moisture Sensitive；Air Sensitive
• Indice de réfraction: 1.44
• Point d'ébullition (°C): 63°C/15mmHg
• Poids moléculaire: 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