82730
4－吡啶甲醛
purum, ≥96.0% (GC)
别名:
吡啶-4-甲醛
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关于此项目
经验公式（希尔记法）:
C6H5NO
化学文摘社编号:
分子量:
107.11
EC Number:
212-832-3
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
105342
MDL number:
grade
purum
assay
≥96.0% (GC)
form
liquid
impurities
≤1% pyridine-2-carboxaldehyde
color
clear brown-yellow
refractive index
n20/D 1.544
bp
71-73 °C/10 mmHg (lit.)
density
1.137 g/mL at 20 °C (lit.)
storage temp.
2-8°C
SMILES string
[H]C(=O)c1ccncc1
InChI
1S/C6H5NO/c8-5-6-1-3-7-4-2-6/h1-5H
InChI key
BGUWFUQJCDRPTL-UHFFFAOYSA-N
Other Notes
用于为酶的固定化制备含吡啶的聚合物（玻璃珠）
signalword
Danger
hcodes
Hazard Classifications
Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 1
flash_point_f
172.0 °F
flash_point_c
77.8 °C
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
F. Pittner et al.
Journal of the American Chemical Society, 102, 2451-2451 (1980)
F. Pittner et al.
Enzyme Eng., 5, 447-447 (1980)
Mohini Bhadwal et al.
Molecular imaging and biology : MIB : the official publication of the Academy of Molecular Imaging, 17(1), 111-118 (2014-07-20)
Porphyrins have inherent ability to localize preferentially in tumor lesions. Cationic porphyrins are readily water soluble and reported to exhibit strong DNA-binding capabilities. Therefore, attempt has been made to prepare a water soluble [(68)Ga]-labeled cationic porphyrin, viz., 5,10,15,20-tetra(4-methylpyridyl)porphyrin (TMP), and
Jan Hintzpeter et al.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 29(1), 263-273 (2014-11-08)
The purpose of this study was to investigate the origin and function of the aldo-keto reductase (AKR) superfamily as enzymes involved in the detoxification of xenobiotics. We used the cyanobacterium Synechocystis sp. PCC 6803 as a model organism and sequence
Artak Tovmasyan et al.
Journal of inorganic biochemistry, 140, 94-103 (2014-08-03)
In the present study we have synthesized a novel amphiphilic porphyrin and its Ag(II) complex through modification of water-soluble porphyrinic structure in order to increase its lipophilicity and in turn pharmacological potency. New cationic non-symmetrical meso-substituted porphyrins were characterized by
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