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Merck
CN

156884

3-Nitrophthalic anhydride

98%

Synonym(s):

3-Nitrophthalic acid anhydride, 4-Nitro-2-benzofuran-1,3-dione, 4-Nitroisobenzofuran-1,3-dione

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About This Item

Empirical Formula (Hill Notation):
C8H3NO5
CAS Number:
Molecular Weight:
193.11
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
EC Number:
211-373-6
Beilstein/REAXYS Number:
179963
MDL number:
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Quality Level

assay

98%

form

solid

mp

163-165 °C (lit.)

SMILES string

[O-][N+](=O)c1cccc2C(=O)OC(=O)c12

InChI

1S/C8H3NO5/c10-7-4-2-1-3-5(9(12)13)6(4)8(11)14-7/h1-3H

InChI key

ROFZMKDROVBLNY-UHFFFAOYSA-N

Application

Reactions with aminoquinazolinones yield phthalimidoquinazolinones.


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signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

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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J. Serb. Chem. Soc., 57, 629-629 (1992)
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
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



Global Trade Item Number

SKUGTIN
156884-25G04061838742964
156884-5G04061833013922