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About This Item
Linear Formula:
CH3P(O)(OC2H5)2
CAS Number:
Molecular Weight:
152.13
UNSPSC Code:
12352108
NACRES:
NA.22
PubChem Substance ID:
EC Number:
211-667-4
Beilstein/REAXYS Number:
1753416
MDL number:
Assay:
97%
InChI key
NYYLZXREFNYPKB-UHFFFAOYSA-N
InChI
1S/C5H13O3P/c1-4-7-9(3,6)8-5-2/h4-5H2,1-3H3
SMILES string
CCOP(C)(=O)OCC
assay
97%
reaction suitability
reaction type: C-C Bond Formation
Quality Level
refractive index
n20/D 1.414 (lit.)
bp
194 °C (lit.)
density
1.041 g/mL at 25 °C (lit.)
functional group
phosphonate
Related Categories
Application
Reactant for the synthesis of:
- Fluoroalkyl α- and β-aminophosphonates
- Acyclic nucleoside phosphonates with branched phosphonoethoxy-Et chains as potential antivirals
- Difluoromethyl arylphosphonates
- Pyridone alkaloids with neuritogenic activity
- Lipophilic meropenem-derived prodrugs
- Phomactin cyclohexane core and diterpenoid framework
- Phosphonylated peptides via solid-phase synthesis
Reagent employed in the synthesis of α-alkenyl, γ-hydroxyl, and dialkyl fluoroalkynyl phosphonates.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
10 - Combustible liquids
flash_point_f
167.0 °F - closed cup
flash_point_c
75 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
监管及禁止进口产品
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Synthetic Communications, 21, 2341-2341 (1991)
Ying Zhang et al.
Biomaterials, 26(33), 6736-6742 (2005-06-07)
Novel BAB type amphiphilic triblock copolymers consisting of poly (ethylene glycol) (PEG) (B) as hydrophilic segment and poly (epsilon-caprolactone) (PCL) (A) as hydrophobic block were prepared by coupling reaction using L-lysine methyl ester diisocyanate (LDI) as the chain extender. The
E Maurelli et al.
Free radical biology & medicine, 27(1-2), 34-41 (1999-08-12)
The spin trap 5-(diethoxyphosphoryl)-5-methyl-1-pyrroline N-oxide (DEPMPO) is an improved ESR probe to assess superoxide (O2*-) formation in the postischemic heart. We recently found that DEPMPO pretreatment improves recovery of cardiac function with the concomitant inhibition of postischemic O2*- production. By
The Journal of Organic Chemistry, 58, 5779-5779 (1993)
Journal of the Chemical Society. Perkin Transactions 1, 2153-2153 (1993)
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