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241369

2-苯基丙醛

Name: 2-苯基丙醛
Brand: ALDRICH

98%

别名:

氢化阿托醛, 龙葵醛

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关于此项目

线性分子式:

CH₃CH(C₆H₅)CHO

化学文摘社编号:

93-53-8

分子量:

134.18

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24854478

EC Number:

202-255-5

Beilstein/REAXYS Number:

1905601

MDL number:

MFCD00006973

Assay:

98%

Form:

liquid

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属性

Quality Level

100

assay

98%

form

liquid

refractive index

n20/D 1.517 (lit.)

bp

92-94 °C/12 mmHg (lit.)

density

1.002 g/mL at 25 °C (lit.)

functional group

aldehyde, phenyl

storage temp.

2-8°C

SMILES string

[H]C(=O)C(C)c1ccccc1

InChI

1S/C9H10O/c1-8(7-10)9-5-3-2-4-6-9/h2-8H,1H3

InChI key

IQVAERDLDAZARL-UHFFFAOYSA-N

说明

Application

以 2-苯丙醛 (hydratropaldehyde) 为底物，研究重组肌红蛋白 rMB (1) 的变形活性。

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存储类别

10 - Combustible liquids

wgk

WGK 1

flash_point_f

174.2 °F

flash_point_c

79 °C

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Reductive activation of dioxygen by a myoglobin reconstituted with a flavohemin.

Takashi Matsuo et al.

Journal of the American Chemical Society, 124(38), 11234-11235 (2002-09-19)

We successfully converted myoglobin, an oxygen-storage hemoprotein, into an oxygen-activating hemoprotein like cytochrome P450s by replacing the native hemin with the artificially created flavohemin. The reconstituted myoglobin, rMb(1), was chacterized by ESI-TOF-mass, UV-vis, and fluorescence spectra. The 1H NMR spectrum

Synthesis and in vitro reactivity of 3-carbamoyl-2-phenylpropionaldehyde and 2-phenylpropenal: putative reactive metabolites of felbamate.

C D Thompson et al.

Chemical research in toxicology, 9(8), 1225-1229 (1996-12-01)

We propose that 3-carbamoyl-2-phenylpropionaldehyde is an intermediate in the metabolism of felbamate, an anti-epileptic drug with a unique profile of the therapeutic activity, and undergoes a cascade of chemical reactions responsible for the toxic properties of the parent drug. To

Stability and comparative metabolism of selected felbamate metabolites and postulated fluorofelbamate metabolites by postmitochondrial suspensions.

Robert J Parker et al.

Chemical research in toxicology, 18(12), 1842-1848 (2005-12-20)

Evidence has been presented suggesting that a reactive metabolite, 2-phenylpropenal (ATPAL), may be responsible for the toxicities observed during therapy with the antiepileptic drug felbamate (FBM). Formation of ATPAL from its unstable immediate precursor, 3-carbamoyl-2-phenylpropionaldedhyde (CBMA) requires the loss of

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全球贸易项目编号

货号	GTIN
241369-100G	04061825092096