I17451
异烟酰胺
ReagentPlus®, 99%
别名:
吡啶-4-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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
215-926-2
Beilstein/REAXYS Number:
2173
MDL number:
Assay:
99%
product line
ReagentPlus®
assay
99%
mp
155-157 °C (lit.)
SMILES string
NC(=O)c1ccncc1
InChI
1S/C6H6N2O/c7-6(9)5-1-3-8-4-2-5/h1-4H,(H2,7,9)
InChI key
VFQXVTODMYMSMJ-UHFFFAOYSA-N
Application
异烟酰胺（吡啶-4-甲酰胺）可作为合成以下物质的杂环结构单元：
它还可用作共晶试剂（co-former）,与活性药物成分（API）一起制备共晶体。
- 潜在抗结核剂4-氧代-1,3-噻嗪烷-3-基异烟酰胺衍生物。
- 通过合成氨基磷酸酯配体制备的用于各种生物活性研究的异烟酰胺有机锡 (IV) 复合物。
- 2-(羟基亚氨基)-N-(吡啶-3-基)乙酰胺的双吡啶鎓异烟酰胺衍生物，其是一种强效活化剂沙林
它还可用作共晶试剂（co-former）,与活性药物成分（API）一起制备共晶体。
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
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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
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Journal of Organometallic Chemistry, 695(9), 1383-1391 (2010)
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European journal of pharmacology, 609(1-3), 13-18 (2009-03-17)
The phytoalexin resveratrol has been described to have chemopreventive and chemotherapeutic effects in several tumor models while its effects on osteosarcoma have not been extensively studied. Additionally, resveratrol is a potent activator of the Sirt1/Sir2 (silent information regulator 2) family
Srinu Tothadi et al.
Philosophical transactions. Series A, Mathematical, physical, and engineering sciences, 370(1969), 2900-2915 (2012-05-23)
The idea of a structural landscape is based on the fact that a large number of crystal structures can be associated with a particular organic molecule. Taken together, all these structures constitute the landscape. The landscape includes polymorphs, pseudopolymorphs and
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| I17451-100G | 04061833076613 |
| I17451-25G | 04061833848005 |