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238201

Sigma-Aldrich

4-Nitrophthalic anhydride

92%

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About This Item

Empirical Formula (Hill Notation):
C8H3NO5
CAS Number:
5466-84-2
Molecular Weight:
193.11
Beilstein:
179682
EC Number:
226-776-2
MDL number:
MFCD00005922
UNSPSC Code:
12162002
PubChem Substance ID:
24854147
NACRES:
NA.23

Assay

92%

impurities

5-8% 3-nitrophthalic anhydride

mp

116-120 °C (lit.)

SMILES string

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

InChI

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

InChI key

MMVIDXVHQANYAE-UHFFFAOYSA-N

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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

238201-25G:
238201-5G:
238201-VAR:
238201-BULK:

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Vu H Nguyen et al.
EJNMMI research, 3(1), 80-80 (2013-12-18)
Sigma2 (σ2) receptors are highly expressed in cancer cell lines and in tumours. Two novel selective 18F-phthalimido σ2 ligands, 18F-SIG343 and 18F-SIG353, were prepared and characterised for their potential tumour imaging properties. Preparation of 18F-SIG343 and 18F-SIG353 was achieved via
Kalyan K Sethi et al.
Pharmaceuticals (Basel, Switzerland), 14(7) (2021-08-07)
New derivatives were synthesised by reaction of amino-containing aromatic sulphonamides with mono-, bi-, and tricyclic anhydrides. These sulphonamides were investigated as human carbonic anhydrases (hCAs, EC 4.2.1.1) I, II, IX, and XII inhibitors. hCA I was inhibited with inhibition constants
Nasimossadat Banarouei et al.
Mini reviews in medicinal chemistry, 19(8), 679-687 (2018-04-26)
N-aryl derivatives of phthalimide and 4-nitro phthalimide have demonstrated cyclooxygenase inhibitory activity. Also, they possess excellent analgesic and antiinflammatory activity. In this work, a new series of N-arylmethylideneamino derivatives of phthalimide and 4-nitro phthalimide were designed and synthesized. The designed

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