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关于此项目
线性分子式:
(C2H5O)2P(O)CH2CO2C(CH3)3
化学文摘社编号:
分子量:
252.24
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352108
MDL number:
Assay:
95%
Form:
liquid
assay
95%
form
liquid
reaction suitability
reaction type: C-C Bond Formation
refractive index
n20/D 1.431 (lit.)
bp
100-103 °C/1.5 mmHg (lit.)
density
1.074 g/mL at 25 °C (lit.)
functional group
ester, phosphonate
SMILES string
CCOP(=O)(CC(=O)OC(C)(C)C)OCC
InChI
1S/C10H21O5P/c1-6-13-16(12,14-7-2)8-9(11)15-10(3,4)5/h6-8H2,1-5H3
InChI key
NFEGNISFSSLEGU-UHFFFAOYSA-N
Application
Reactant for:
- Preparation of ydroxymethylated dihydroxyvitamin D3 analogs via Wittig-Horner approach, as potential antitumor agents
- Synthesis of phosphopeptide mimetic prodrugs targeted to Src homology 2 (SH2) domain of signal transducer and activator of transcription 3 (Stat 3)
- One-pot synthesis of the DPP4-selective inhibitor ABT-341 by a four-component coupling mediated by a diphenylprolinol silyl ether
- Bicyclic triaminophosphine-promoted stereoselective synthesis of a,β-unsaturated esters, fluorides, and nitriles from aldehydes and ketones using Wadsworth-Emmons phosphonates
- Preparation of amidopropenyl hydroxamates as human histone deacetylase (HDAC) inhibitors
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves