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332097

Sigma-Aldrich

4-Nitrophthalimide

98%

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Empirical Formula (Hill Notation):
C8H4N2O4
CAS Number:
Molecular Weight:
192.13
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.47

Quality Level

Assay

98%

form

powder

mp

195-199 °C (lit.)

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

SMILES string

[O-][N+](=O)c1ccc2C(=O)NC(=O)c2c1

InChI

1S/C8H4N2O4/c11-7-5-2-1-4(10(13)14)3-6(5)8(12)9-7/h1-3H,(H,9,11,12)

InChI key

ANYWGXDASKQYAD-UHFFFAOYSA-N

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1 of 4

This Item
414034370061D4645
4-Nitrophthalimide 98%

Sigma-Aldrich

332097

4-Nitrophthalimide

3-Nitrophthalimide 97%

Sigma-Aldrich

414034

3-Nitrophthalimide

form

powder

form

powder or crystals

form

powder, crystals or chunks

form

powder

mp

195-199 °C (lit.)

mp

213-215 °C (lit.)

mp

136-138 °C (lit.)

mp

>300 °C

application(s)

diagnostic assay manufacturing
hematology
histology

application(s)

diagnostic assay manufacturing
hematology
histology

application(s)

diagnostic assay manufacturing
hematology
histology

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

storage temp.

room temp

storage temp.

room temp

storage temp.

room temp

Quality Level

100

Quality Level

200

Quality Level

200

Quality Level

200

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Asghar Davood et al.
Medicinal chemistry (Shariqah (United Arab Emirates)), 8(5), 953-963 (2012-06-30)
A series of compounds including N-aryl substituents of phthalimide and 4-nitrophthalimide were synthesized and evaluated for their anticonvulsant properties. The in vivo screening data suggest that all the analogs have the ability to protect against pentylenetetrazole-induced seizures. These compounds exerted
Axel G Griesbeck et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 9(10), 1385-1390 (2010-09-08)
The chiral chemosensor 1, based on a thiourea-activated phthalimide, is available by four reaction steps from 4-nitrophthalimide. 1 detects fluoride, chloride, acetate, and dihydrogen phosphate anions by changes in UV-vis absorption. Fluoride in excess induces deprotonation whereas the other anions
N Takihi et al.
Mutagenesis, 8(3), 257-264 (1993-05-01)
A method is described for using the fragments identified by the CASE structure-activity relational expert system to identify the type of chemicals that require further testing in mutagenicity and clastogenicity assays. Inclusion of such chemicals will increase the informational content
Yue Sun et al.
Biomaterials, 117, 77-91 (2016-12-13)
Photodynamic therapy (PDT) has already shown immense potential in antitumor fields due to its low systemic toxicity and negligible drug resistance. However, the clinical application of current photosensitizers is still restricted by the low singlet oxygen yield or insolubility. Herein
Jun Yang et al.
Biotechnology and applied biochemistry, 66(1), 33-42 (2018-09-20)
A nitroreductase-encoded gene from an efficient nitro-reducing bacterium Streptomyces mirabilis DUT001, named snr, was cloned and heterogeneously expressed in Escherichia coli. The purified Streptomyces nitroreductase SNR was a homodimer with an apparent subunit molecular weight of 24 kDa and preferred NADH

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