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250031

(R)-N-3,5-二硝基苯甲酰基苯甘氨酸

Name: (<I>R</I>)-<I>N</I>-3,5-二硝基苯甲酰基苯甘氨酸
Brand: ALDRICH

99%, for peptide synthesis

别名:

N-(3,5-二硝基苯甲酰)-D-α-苯基甘氨酸, R-(-)-N-(3,5-二硝基苯甲酰)-α-苯基甘氨酸

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关于此项目

线性分子式:

(O₂N)₂C₆H₃CONHCH(C₆H₅)CO₂H

化学文摘社编号:

74927-72-3

分子量:

345.26

NACRES:

NA.22

PubChem Substance ID:

24855029

UNSPSC Code:

12352209

MDL number:

MFCD00010134

Beilstein/REAXYS Number:

4719763

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属性

产品名称

(R)-N-3,5-二硝基苯甲酰基苯甘氨酸, 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

说明

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

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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

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

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)

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货号	GTIN
250031-5G	04061838347992