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Merck
CN

104051

吡啶酰胺

98%

别名:

2-吡啶甲酰胺

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关于此项目

经验公式(希尔记法):
C6H6N2O
化学文摘社编号:
分子量:
122.12
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
215-921-5
MDL number:
Assay:
98%
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Quality Level

assay

98%

mp

110 °C (dec.) (lit.)

functional group

amide

SMILES string

NC(=O)c1ccccn1

InChI

1S/C6H6N2O/c7-6(9)5-3-1-2-4-8-5/h1-4H,(H2,7,9)

InChI key

IBBMAWULFFBRKK-UHFFFAOYSA-N

Application

以吡啶酰胺为模板制备分子印迹聚合物 。在一项研究中,吡啶酰胺被用于评估吡啶酰胺从HClO 4 中的铬(III) - 吡啶酰胺络合物中释放的动力学和机理。

Biochem/physiol Actions

吡啶酰胺是大鼠胰岛细胞核多聚(ADP-核糖)合成酶的潜在抑制剂 。吡啶酰胺充当二齿配体并与镧系元素硝酸盐,硫氰酸盐和高氯酸盐形成配合物。


pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Bambang Kuswandi et al.
Analytica chimica acta, 591(2), 208-213 (2007-05-08)
A disposable ion-selective optode for mercury based on trityl-picolinamide (T-Pico) as neutral ionophore was developed. The sensing layer consist of plasticised PVC incorporating T-Pico as a selective ionophore for Hg2+, ETH 5418 as a chromoionophore, and potassium tetrakis[3,5-bis(trifluoromethyl)phenyl] borate as
Jeremy L Yap et al.
Organic & biomolecular chemistry, 10(15), 2928-2933 (2012-03-08)
By conducting a structure-activity relationship study of the backbone of a series of oligoamide-foldamer-based α-helix mimetics of the Bak BH3 helix, we have identified especially potent inhibitors of Bcl-x(L). The most potent compound has a K(i) value of 94 nM
Protection by picolinamide, a novel inhibitor of poly (ADP-ribose) synthetase, against both streptozotocin-induced depression of proinsulin synthesis and reduction of NAD content in pancreatic islets.
H Yamamoto et al.
Biochemical and biophysical research communications, 95(1), 474-481 (1980-07-16)



全球贸易项目编号

货号GTIN
104051-50G04061832540856
104051-10G04061838671141