Key Documents

View All Documentation

292966

1,1′-Binaphthyl-2,2′-diyl hydrogenphosphate

Name: 1,1&#8242;-Binaphthyl-2,2&#8242;-diyl hydrogenphosphate
Brand: ALDRICH

95%, solid

Synonym(s):

BNDHP

Select a Size

Change View

About This Item

Empirical Formula (Hill Notation):

C₂₀H₁₃O₄P

CAS Number:

35193-63-6

Molecular Weight:

348.29

NACRES:

NA.22

PubChem Substance ID:

24857622

UNSPSC Code:

12352005

EC Number:

252-425-8

MDL number:

MFCD00010045

Technical Service

Need help? Our team of experienced scientists is here for you.

Let Us Assist

Properties

Product Name

1,1′-Binaphthyl-2,2′-diyl hydrogenphosphate, 95%

Quality Level

100

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

SMILES string

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 key

JEHUZVBIUCAMRZ-UHFFFAOYSA-N

Description

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

新产品

This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

02317DJ

00718JM

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Enantioseparation of atropisomeric 1,1'-binaphthyl-2,2'-diyl hydrogen phosphate in capillary electrophoresis by using di- and oligosaccharides as chiral selectors: di- and oligosaccharide chiral selectors in capillary electrophoresis.

B Chankvetadze et al.

Chirality, 10(1-2), 134-139 (1998-02-21)

Twelve different disaccharides and a series of noncyclic malto- and cello-oligosaccharides were used as chiral selectors in capillary electrophoresis (CE). Most saccharides resolved the enantiomers of atropisomeric 1,1'-binaphthyl-2,2'-diyl hydrogen phosphate (BDHP) depending on the type (alpha or beta) and position

A comparison of ionic liquids to molecular organic solvents as additives for chiral separations in micellar electrokinetic chromatography.

Simon M Mwongela et al.

Journal of separation science, 30(9), 1334-1342 (2007-07-12)

In this study, we report the effects of adding ionic liquids (ILs), as compared to adding conventional molecular organic solvents (MOSs), to aqueous buffer solutions containing molecular micelles in the separation of chiral analyte mixtures in micellar EKC (MEKC). The

Comparison of alkylglycoside surfactants in enantioseparation by capillary electrophoresis.

Y Mechref et al.

Electrophoresis, 18(6), 912-918 (1997-06-01)

Three alkylglycoside surfactants, namely n-octyl-beta-D-glucopyranoside (OG), n-nonyl-beta-D-glucopyranoside (NG), and n-octyl-beta-D-maltopyranoside (OM), were compared in the enantiomeric separation of dansyl amino acids, binaphthyl phosphate, bupivacaine and warfarin. While only OM exhibited an enantioselectivity toward warfarin, bupivacaine, and dansyl tryptophan, all three

View All Related Papers

Global Trade Item Number

SKU	GTIN
292966-5G	04061833371978