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Merck

248940

Sigma-Aldrich

S-联萘酚磷酸酯

97%

别名:

(S)-(+)-1,1′-联萘-2,2′-二基磷酸氢酯, (S)-4-羟基二萘并[2,1-d:1′,2′-f][1,3,2]二噁磷杂庚英-4-氧化物

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About This Item

经验公式(希尔记法):
C20H13O4P
CAS号:
分子量:
348.29
Beilstein:
4787775
MDL號碼:
分類程式碼代碼:
12352005
PubChem物質ID:
NACRES:
NA.22

化驗

97%

形狀

solid

光學活性

[α]22/D +595°, c = 1.35 in methanol

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

相关类别

應用

用作不对称 Mannich 反应中手性布朗斯特酸催化剂。

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

防範說明

危險分類

Skin Irrit. 2

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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Masahiro Yamanaka et al.
Journal of the American Chemical Society, 129(21), 6756-6764 (2007-05-05)
Mannich-type reaction of ketene silyl acetals with aldimines proceeded catalytically by means of a phosphoric acid diester, derived from (R)-BINOL, as a chiral Brønsted acid to afford beta-amino esters with good diastereoselectivity in favor of the syn isomer and high
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)

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