Key Documents

View All Documentation

250031

(R)-(−)-N-(3,5-Dinitrobenzoyl)-α-phenylglycine

Name: (<I>R</I>)-(&#8722;)-<I>N</I>-(3,5-Dinitrobenzoyl)-&#945;-phenylglycine
Brand: ALDRICH

99%, for peptide synthesis

Synonym(s):

N-(3,5-Dinitrobenzoyl)-D-α-phenylglycine, R-(−)-N-(3,5-Dinitrobenzoyl)phenylglycine

Select a Size

Change View

About This Item

Linear Formula:

(O₂N)₂C₆H₃CONHCH(C₆H₅)CO₂H

CAS Number:

74927-72-3

Molecular Weight:

345.26

NACRES:

NA.22

PubChem Substance ID:

24855029

UNSPSC Code:

12352209

MDL number:

MFCD00010134

Beilstein/REAXYS Number:

4719763

Technical Service

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

Let Us Assist

Properties

Product Name

(R)-(−)-N-(3,5-Dinitrobenzoyl)-α-phenylglycine, 99%

assay

99%

optical activity

[α]20/D −102°, c = 0.9 in THF

reaction suitability

reaction type: solution phase peptide synthesis

mp

216-217 °C (lit.)

application(s)

peptide synthesis

SMILES string

OC(=O)[C@H](NC(=O)c1cc(cc(c1)[N+]([O-])=O)[N+]([O-])=O)c2ccccc2

InChI

1S/C15H11N3O7/c19-14(16-13(15(20)21)9-4-2-1-3-5-9)10-6-11(17(22)23)8-12(7-10)18(24)25/h1-8,13H,(H,16,19)(H,20,21)/t13-/m1/s1

InChI key

MIVUDAUOXJDARR-CYBMUJFWSA-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

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

Resolution of enantiomers of 19-hydroxyeicosatetraenoate and 18-hydroxyeicosatetraenoate by chiral phase high-performance liquid chromatography of naphthoyl ester derivatives.

E H Oliw

Journal of chromatography, 526(2), 525-529 (1990-04-06)

Capillary electrophoresis with (R)-(--)-N-(3,5-dinitrobenzoyl)-alpha-phenylglycine as chiral selector for separation of albendazole sulfoxide enantiomers and their analysis in human plasma.

Wolfgang Thormann et al.

Journal of pharmaceutical and biomedical analysis, 27(3-4), 555-567 (2002-01-05)

The electrokinetic separation and analysis of the enantiomers of albendazole sulfoxide (ABZSO), a sulfoxide with a sulfur stereogenic center hepatically formed during therapy with the anthelmintic drug albendazole (ABZ), is reported. Using aqueous or nonaqueous alkaline background electrolytes, ABZSO enantiomers

QSAR of matrix metalloproteinase inhibitor N-[(substituted phenyl)sulfonyl]-N-4-nitrobenzylglycine hydroxamates using LFER model.

K Roy et al.

Drug design and discovery, 17(4), 315-323 (2002-01-05)

QSAR analyses of matrix metalloproteinase (MMP) inhibitor N-[(substituted phenyl)sulfonyl]-N-4-nitrobenzylglycine hydroxamates, recently reported by Scozzafava and Supuran, have been attempted using linear free energy related (LFER) model of Hansch to explore the contribution patterns of the phenyl ring substitutions (P1' anchoring

View All Related Papers

Global Trade Item Number

SKU	GTIN
250031-5G	04061838347992