292966
联萘酚磷酸酯
95%, solid
别名:
BNDHP
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关于此项目
经验公式（希尔记法）:
C20H13O4P
化学文摘社编号:
分子量:
348.29
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352005
EC Number:
252-425-8
MDL number:
产品名称
联萘酚磷酸酯, 95%
InChI key
JEHUZVBIUCAMRZ-UHFFFAOYSA-N
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)
SMILES string
OP1(=O)Oc2ccc3ccccc3c2-c4c(O1)ccc5ccccc45
assay
95%
form
solid
reaction suitability
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
Quality Level
相关类别
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
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
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
Anna Bielejewska et al.
Journal of chromatography. A, 977(2), 225-237 (2002-11-29)
The chiral recognition ability of single and dual selectors, that were used as additives, have been investigated by HPLC and CE. Native beta- and gamma-cyclodextrins, permethylated beta-cyclodextrin, hydroxypropyl-beta-cyclodextrin, cholic acid and taurodeoxycholic acid sodium salts were applied as chiral selectors
Yingying Dong et al.
Electrophoresis, 32(13), 1735-1741 (2011-06-28)
Gels formed by self-association of monomeric guanosine compounds join numerous other agents such as cyclodextrins, crown ethers, chiral surfactants, antibiotics, proteins, and polysaccharides for chiral separations. Guanosine gels (G-gels) are self-assembled networks of hydrogen-bonded tetrads formed by guanosine nucleotides and
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
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