O9328
草酰胺
98%
别名:
乙二酰二胺
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关于此项目
线性分子式:
NH2COCONH2
化学文摘社编号:
分子量:
88.07
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-442-5
Beilstein/REAXYS Number:
1743262
MDL number:
Assay:
98%
Form:
powder
Quality Level
assay
98%
form
powder
mp
>300 °C (lit.)
SMILES string
NC(=O)C(N)=O
InChI
1S/C2H4N2O2/c3-1(5)2(4)6/h(H2,3,5)(H2,4,6)
InChI key
YIKSCQDJHCMVMK-UHFFFAOYSA-N
Application
草酰胺可用于：
- 作为合成例如双（苯并咪唑）和通过与糠醛进行水缩合形成的席夫碱配体的前体。
- 通过与尿素自组装聚合形成碳氮化物（g-C3N4）纳米管。
- 作为合成双核 IrIII配合物[Ir2(μ2-恶酰胺基-N,N′,O,O′)(ptpy)4]的桥联配体，ptpy=2-（对甲苯基）吡啶基。
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2
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
T L Nguyen et al.
Journal of the American Chemical Society, 123(44), 11057-11064 (2001-11-01)
Ureas characteristically form one-dimensional hydrogen-bonded alpha-networks with a repeat distance of about 4.60 A. Oxamides form similar alpha-networks with a longer 5.05 A repeat distance. The urea of glycine and the oxamide of glycine were each cocrystallized with a series
Advancing the n?π* electron transition of carbon nitride nanotubes for H2 photosynthesis
Zhang G, et al.
Journal of Material Chemistry A, 5(25), 12723-12728 (2017)
Synthesis, characterization, and biological and anticancer studies of mixed ligand complexes with Schiff base and 2, 2?-bipyridine
Omar MM, et al.
Applied Organometallic Chemistry, 31(10), e3724-e3724 (2017)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| O9328-100G | 04061838355324 |