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Dimethyl 2-oxoheptylphosphonate_Molecular_structure_CAS_36969-89-8)
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Dimethyl 2-oxoheptylphosphonate

Catalog No. 157937 Name Sigma Aldrich
CAS Number 36969-89-8 Website http://www.sigmaaldrich.com
M. F. C9H19O4P Telephone 1-800-521-8956
M. W. 222.218521 Fax
Purity 85% Email
Storage Chembase ID: 74985

SYNONYMS

Title
(2-氧代庚基)膦酸二甲酯
IUPAC name
dimethyl (2-oxoheptyl)phosphonate
IUPAC Traditional name
dimethyl 2-oxoheptylphosphonate
Synonyms
(2-Oxoheptyl)phosphonic acid dimethyl ester
Dimethyl (hexanoylmethyl)phosphonate

DATABASE IDS

Beilstein Number 1946305
CAS Number 36969-89-8
MDL Number MFCD00009514
EC Number 253-293-4
PubChem SID 24849710

PROPERTIES

Grade technical grade
Linear Formula CH3(CH2)4COCH2P(O)(OCH3)2
Purity 85%
Boiling Point 109 °C/0.4 mmHg(lit.)
Density 1.07 g/mL at 25 °C(lit.)
Flash Point 110 °C
Flash Point 230 °F
Refractive Index n20/D 1.444(lit.)
MSDS Link Download
Personal Protective Equipment Eyeshields, Gloves, half-mask respirator (US), multi-purpose combination respirator cartridge (US)
German water hazard class 3

DETAILS

Description (简体中文)
Application
前列腺素合成的关键中间体。
Reactant for:
• Beirut reaction for the preparation of phosphonylated quinoxaline dioxides1
• Preparation of pyrrolomorphinan derivatives as κ opioid agonists via cyclocondensation, Vilsmeier-Haack formylation, Horner-Wadsworth-Emmons reaction, and Kocienski-modified Julia olefination from naltrexone methyl ether2
• Synthesis of C-glycosides amphiphiles via solvent-free Horner-Wadsworth-Emmons reaction with unprotected sugars3
• Preparation of specific inhibitors of endocannabinoid biosynthesis4
包装
1 g in glass bottle
Description (English)
Application
A key intermediate in prostaglandin synthesis.
Reactant for:
• Beirut reaction for the preparation of phosphonylated quinoxaline dioxides1
• Preparation of pyrrolomorphinan derivatives as κ opioid agonists via cyclocondensation, Vilsmeier-Haack formylation, Horner-Wadsworth-Emmons reaction, and Kocienski-modified Julia olefination from naltrexone methyl ether2
• Synthesis of C-glycosides amphiphiles via solvent-free Horner-Wadsworth-Emmons reaction with unprotected sugars3
• Preparation of specific inhibitors of endocannabinoid biosynthesis4
Packaging
1 g in glass bottle

REFERENCES