Clorofosfito di dietile - ≥95% , CAS No.589-57-1

CAS: 589-57-1 Cat. No.: D123978 Formula: (C₂H₅O)₂PCl Peso molecolare: 156.55 Beilstein Registry Number: 1098392 Numero EC: 209-652-2

GRADE & PURITY ≥95%

Synonyms

AKOS009031586 | SY049944 | (1R)-(+)-(1-AMINO-2-METHYLPROPYL)PHOSPHONICACID | AMY843 | H10781 | Diethyl phosphorochloridite | Ethyl phosphorochloridite, (EtO)2ClP | F414S3V8K6 | (C2H5O)2PCl | Ethyl chlorophosphite | SCHEMBL6274 | DIETHYL PHOSPHOROCHLORIDIT

Storage

Conservare a 2-8°C, con carica di argon

Shipped In

Ghiaccio umido

Panoramica

Agente fosforilante versatile per esteri e lattoni enolati, ammine e alchinoli.

Applicazione: è utilizzato nella sintesi degli organofosfati

Viene utilizzato nella sintesi degli organofosfati e, in base agli studi effettuati, è considerato un agente anticolinesterasico.

Specifications

Sinonimi

AKOS009031586 | SY049944 | (1R)-(+)-(1-AMINO-2-METHYLPROPYL)PHOSPHONICACID | AMY843 | H10781 | Diethyl phosphorochloridite | Ethyl phosphorochloridite, (EtO)2ClP | F414S3V8K6 | (C2H5O)2PCl | Ethyl chlorophosphite | SCHEMBL6274 | DIETHYL PHOSPHOROCHLORIDIT

Specifiche e purezza

≥95%

Condizioni di conservazione di stoccaggio

Conservare a 2-8°C, con carica di argon

Spedito in

Ghiaccio umido

Purezza

≥95%

Nomi e identificatori

• Pubchem Sid: 508812052
• Sorrisi canonici: CCOP(OCC)Cl
• IUPAC Name: chloro(diethoxy)phosphane
• InChIKey: TXHWYSOQHNMOOU-UHFFFAOYSA-N
• INCHI: 1S/C4H10ClO2P/c1-3-6-8(5)7-4-2/h3-4H2,1-2H3
• Isomeri SMILES: CCOP(OCC)Cl
• WGK Germania: 3
• Peso molecolare: 156.55
• Beilstein: 1098392
• Reaxy-Rn: 1098392
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1098392&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Classe Organooxygen compounds

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Classe: Organooxygen compounds
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Organooxygen compounds
• Alternative Parents: Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Hydrocarbon derivative - Organooxygen compound - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as organooxygen compounds. These are organic compounds containing a bond between a carbon atom and an oxygen 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

• Solubilità: Soluble in DMSO and chloroform. Reacts with water.
• Sensibilità: Light & Moisture & Air Moisture Sensitive
• Indice di rifrazione: 1.4375
• Punto di infiammabilità (°F): 33.8 °F
• Punto di infiammabilità (°C): 1°C(Lit.)
• Punto di ebollizione (°C): 153-155°C
• Peso molecolare: 156.550 g/mol
• XLogP3: 1.500
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 156.011 Da
• Monoisotopic Mass: 156.011 Da
• Topological Polar Surface Area: 18.500 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 47.300
• 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

Riferimenti

1. Jinghan Wang, Xiujuan Wang, Ling Wang, Xianchao Du, Hongxia Hao, Anjun Qin, Ben Zhong Tang.  (2026)  Etomidate rapid detection by enzyme-linked immunosorbent assay combined with aggregation-induced emission luminogens.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2026.119205]