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About This Item
經驗公式（希爾表示法）:
C20H13O4P
CAS號碼:
分子量：:
348.29
EC號碼:
MDL號碼:
分類程式碼代碼:
12352005
PubChem物質ID:
NACRES:
NA.22
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品質等級
化驗
95%
形狀
solid
反應適用性
reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
SMILES 字串
OP1(=O)Oc2ccc3ccccc3c2-c4c(O1)ccc5ccccc45
InChI
1S/C20H13O4P/c21-25(22)23-17-11-9-13-5-1-3-7-15(13)19(17)20-16-8-4-2-6-14(16)10-12-18(20)24-25/h1-12H,(H,21,22)
InChI 密鑰
JEHUZVBIUCAMRZ-UHFFFAOYSA-N
相關類別
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
Eyeshields, Gloves, type N95 (US)
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Ulrich Schmitt et al.
Electrophoresis, 25(16), 2801-2807 (2004-09-08)
Comparative enantioseparation of the enantiomers of 1,1'-binaphthyl-2,2'-diyl hydrogen phosphate was performed with cyclodextrin (CD)-modified capillary electrophoresis (CE). Two single isomers, beta-CD, heptakis(2,3,6-tri-O-methyl)-beta-CD (TM-beta-CD), and heptakis(2,6-di-O-methyl)-beta-CD (DM-beta-CD) of 98% purity as well as heptakis(2,3-di-O-acetyl)-beta-CD were used and compared in terms of
Ioannis J Stavrou et al.
Electrophoresis, 34(4), 524-530 (2012-12-05)
In this study, the applicability of a chiral ionic liquid (CIL) as the sole chiral selector in CE was investigated for the first time. In particular, five amino acid ester-based CILs were synthesized and used as additives in the BGE
Stephanie A Kingsbury et al.
Magnetic resonance in chemistry : MRC, 48(3), 184-191 (2010-01-06)
NMR spectroscopy was used to characterize the binding of the chiral compound 1,1'-binaphthyl-2,2'-diyl hydrogen phosphate (BNP) to five molecular micelles with chiral dipeptide headgroups. Molecular micelles have covalent linkages between the surfactant monomers and are used as chiral mobile phase
Fluorescence anisotropy as a measure of chiral recognition.
M E McCarroll et al.
Journal of the American Chemical Society, 123(13), 3173-3174 (2001-07-18)
Christine M Hebling et al.
Langmuir : the ACS journal of surfaces and colloids, 24(24), 13866-13874 (2008-12-05)
Bile salt micelles can be employed as a pseudostationary phase in micellar electrokinetic capillary chromatography (MEKC) separations of chiral analytes. To improve MEKC separations of chiral analytes, a molecular level understanding of micelle aggregation in the presence of analyte is
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