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N-Bromophthalimide, 96%|431557|2439-85-2

N-Bromophthalimide, 96%

Cat. No JK431557_100_G
J&K Chemical

Product Information

Product Name
N-Bromophthalimide, 96%
Brand Name
J&K
Product Number
431557
CAS
2439-85-2
Molecular Formula
C8H4BrNO2
Molecular Weight
226.03
SDS Document
View/Download
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
75542
IUPAC Name
2-bromoisoindole-1,3-dione
InChI Key
MARXMDRWROUXMD-UHFFFAOYSA-N
SMILES
C1=CC=C2C(=C1)C(=O)N(C2=O)Br

Properties

Melting Point
204-210

Safety Information

Signal Word
Warning
Hazard Statement
H315
H319
H335
Precautionary Statement
P280
P321
P261
P271
P319
P405
P501
P302+P352
P332+P317
P362+P364
P264+P265
P305+P351+P338
P337+P317
P304+P340
P403+P233

References Data Source From Pubchem

Direct regioselective C-3 halogenation of pyridines
Publication Name: Nature Synthesis
Publication Date: 2025-11-05
DOI: 10.1038/s44160-025-00915-3

Recent advances in silver-mediated/catalyzed synthesis of trifluoromethoxy compounds
Publication Name: Science China Chemistry
Publication Date: 2024-11-04
DOI: 10.1007/s11426-024-2342-4

Photoinduced generation of alkyl and phthalimide nitrogen radicals from N-hydroxyphthalimide esters for the synthesis of benzophenone-type bioisosteres
Publication Name: Science China Chemistry
Publication Date: 2024-08-15
DOI: 10.1007/s11426-024-2107-3

Employing supramolecular chemistry strategies for the separation of mixtures of anisole and bromoanisole isomers
Publication Name: Journal of Inclusion Phenomena and Macrocyclic Chemistry
Publication Date: 2024-04-23
DOI: 10.1007/s10847-024-01242-4

Trifluoromethoxylating Reagents and Summary of Nucleophilic Synthetic Protocols
Publication Name: Science of Synthesis
Publication Date: 2024

N-Bromophthalimide, 96%

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