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Merck
CN

72800

Supelco

4-硝基苯甲醛

for spectrophotometric det. of amino sugars, ≥99.0%

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About This Item

线性分子式:
O2NC6H4CHO
CAS号:
分子量:
151.12
Beilstein:
386796
EC 号:
MDL编号:
UNSPSC代码:
12000000
PubChem化学物质编号:
NACRES:
NA.21

质量水平

方案

≥99.0% (HPLC)
≥99.0%

表单

powder

质量

for spectrophotometric det. of amino sugars

技术

UV/Vis spectroscopy: suitable

灼烧残渣

≤0.05%

mp

103-106 °C (lit.)
104-106 °C

SMILES字符串

[O-][N+](=O)c1ccc(C=O)cc1

InChI

1S/C7H5NO3/c9-5-6-1-3-7(4-2-6)8(10)11/h1-5H

InChI key

BXRFQSNOROATLV-UHFFFAOYSA-N

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其他说明

分光光度法测定氨基碳水化合物的试剂

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Sens. 1

储存分类代码

11 - Combustible Solids

WGK

WGK 2

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


历史批次信息供参考:

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A. Nakamura et al.
Chemical & Pharmaceutical Bulletin, 17, 770-770 (1969)
Mikhail Yu Karganov et al.
Biological trace element research, 198(2), 567-574 (2020-03-08)
The objective of the present study was investigation of tissue trace element distribution in a streptozotocin model of DM1 in rats. DM1 was modeled in 2-month-old male Wistar rats (n = 30) using intraperitoneal injection of 45 mg/kg b.w. (STZ1) and 55 mg/kg b.w.
Zhuo Tang et al.
Organic letters, 6(13), 2285-2287 (2004-06-18)
[reaction: see text] L-Proline-based small peptides have been developed as efficient catalysts for the asymmetric direct aldol reactions of hydroxyacetone with aldehydes. Chiral 1,4-diols 7, which are disfavored products in similar aldol reactions catalyzed by either aldolases or L-proline, were
Anant Prakash et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 76(3-4), 356-362 (2010-04-27)
The new Schiff bases N,N'-bis (4-nitro benzaldehyde) ethylenediamine (L(1)) and N,N'-bis (acetophenone) ethylenediamine (L(2)) and its Zn(II), Cd(II) complexes were synthesized and characterized by different physicochemical studies. Vibrational spectra indicate coordination of metal ion through azomethine nitrogen and acetate/nitrate ions.
Chao Li et al.
Journal of biotechnology, 150(4), 539-545 (2010-10-21)
Several proteases, especially pepsin, were observed to directly catalyze asymmetric aldol reactions. Pepsin, which displays well-documented proteolytic activity under acidic conditions, exhibited distinct catalytic activity in a crossed aldol reaction between acetone and 4-nitrobenzaldehyde with high yield and moderate enantioselectivity.

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