565415
Diethyl allylphosphonate
98%
동의어(들):
2-Propenyl-phosphonic acid diethyl ester
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크기 선택
제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
CH2=CHCH2P(O)(OC2H5)2
CAS 번호:
Molecular Weight:
178.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352108
MDL number:
Assay:
98%
assay
98%
InChI
1S/C7H15O3P/c1-4-7-11(8,9-5-2)10-6-3/h4H,1,5-7H2,2-3H3
SMILES string
CCOP(=O)(CC=C)OCC
InChI key
YPJHXRAHMUKXAE-UHFFFAOYSA-N
reaction suitability
reaction type: C-C Bond Formation
refractive index
n20/D 1.4340 (lit.)
bp
46 °C/0.35 mmHg (lit.)
bulk density
1.022 g/mL
functional group
phosphonate
Quality Level
Application
Reactant for:
- Copolymerization of phosphonated allyl monomers and maleic anhydride
- Enantioselective synthesis of solamin type mono-THF acetogenins
- RCM reaction yielding oxaphospholene and oxaphosphinene heterocycles
- Synthesis of spongistatin 2 using Wittig coupling
- Stereoselective synthesis of pentacyclic furanosteroids
- Preparation of protected polyhydroxylated β -amino acid constitutents of microsclerodermins
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
저장 등급
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Elizabeth I Parkinson et al.
Nature chemical biology, 15(11), 1049-1056 (2019-08-28)
Fosmidomycin and related molecules comprise a family of phosphonate natural products with potent antibacterial, antimalarial and herbicidal activities. To understand the biosynthesis of these compounds, we characterized the fosmidomycin producer, Streptomyces lavendulae, using biochemical and genetic approaches. We were unable
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