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经验公式(希尔记法):
C8H3NO5
化学文摘社编号:
分子量:
193.11
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
EC Number:
211-373-6
Beilstein/REAXYS Number:
179963
MDL number:
产品名称
3-硝基邻苯二甲酸酐, 98%
InChI key
ROFZMKDROVBLNY-UHFFFAOYSA-N
InChI
1S/C8H3NO5/c10-7-4-2-1-3-5(9(12)13)6(4)8(11)14-7/h1-3H
SMILES string
[O-][N+](=O)c1cccc2C(=O)OC(=O)c12
assay
98%
form
solid
mp
163-165 °C (lit.)
Quality Level
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Application
与氨基喹唑啉酮反应生成苯二酰亚氨基喹唑啉酮。
signalword
Warning
hcodes
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
Koichiro Teshima et al.
Journal of pharmaceutical and biomedical analysis, 47(3), 560-566 (2008-03-04)
A liquid chromatography-tandem mass spectrometric (LC-MS/MS) method following chemical derivatization with 3-nitrophtalic anhydride was developed for the simultaneous determination of farnesol and geranylgeraniol in rat liver and testis. One analogue compound of the analytes, n-pentadecanol, was used as an internal
J. Serb. Chem. Soc., 57, 629-629 (1992)
M Pawlowska et al.
Journal of chromatography. A, 666(1-2), 485-491 (1994-04-22)
New pre-column derivatizing reagents: phthalic anhydride, 3-nitrophthalic anhydride, diphenic anhydride, 1,8-naphthalic anhydride and diphenylmaleic anhydride have been developed for resolving chiral compounds having amine groups. Although all of these agents produce derivatives with high molar absorptivities, the later two also
Mauro Vieira de Almeida et al.
Chemical & pharmaceutical bulletin, 55(2), 223-226 (2007-02-03)
Fourteen thalidomide analogs bearing two phthalimido units were prepared in high yields (83-94%) by condensation of different diamines with phthalic or 3-nitrophthalic anhydride. An in vitro investigation of the compounds as inhibitors of the TNF-alpha production was performed. The inhibition
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