Diethyl chlorophosphite - ≥95% , CAS No.589-57-1

CAS: 589-57-1 Cat. No.: D123978 Summenformel: (C₂H₅O)₂PCl Molekulargewicht: 156.55 Beilstein Registry Number: 1098392 EG-Nummer: 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

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Übersicht

Diethyl chlorophosphite can be used as a:
Reducing agent for the reduction of nitro compounds to the corresponding amines.
Deoxygenating agent to reduce pyridine N-oxide to pyridine.
Reagent in the conversion of aldoximes to nitriles via dehydration.

Specifications

Synonyme

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

Spezifikationen & Reinheit

≥95%

Storage

Store at 2-8°C,Argon charged

Verschickt in

Wet ice

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Reinheit

≥95%

Namen und Kennungen

• Pubchem Sid: 508812052
• Kanonisches Lächeln: 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
• Isomere SMILES: CCOP(OCC)Cl
• WGK Deutschland: 3
• Molekulargewicht: 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
    • Klasse Organooxygen compounds

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Klasse: 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
• Beschreibung: 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

Chemische und physikalische Eigenschaften

• Löslichkeit: Soluble in DMSO and chloroform. Reacts with water.
• Empfindlichkeit: Light & Moisture & Air Moisture Sensitive
• Brechungsindex: 1.4375
• Flammpunkt (°F): 33.8 °F
• Flammpunkt (°C): 1°C(Lit.)
• Siedepunkt (°C): 153-155°C
• Molekulargewicht: 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

Referenzen

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]