2,5-Dioxopyrrolidin-1-yl 4-nitrobenzoate

Base Information

• Chemical Name: 2,5-Dioxopyrrolidin-1-yl 4-nitrobenzoate
• CAS No.: 30364-58-0
• Molecular Formula: C11H8N2O6
• Molecular Weight: 264.194
• DSSTox Substance ID: DTXSID30366868
• Nikkaji Number: J428.432A
• Wikidata: Q82152318
• Mol file: 30364-58-0.mol

Synonyms:2,5-Dioxopyrrolidin-1-yl 4-nitrobenzoate;30364-58-0;2,5-Pyrrolidinedione, 1-[(4-nitrobenzoyl)oxy]-;N-[4-(p-Nitrobenzoyl)oxy]succininide;(2,5-dioxopyrrolidin-1-yl) 4-nitrobenzoate;Oprea1_351094;SCHEMBL3735204;DTXSID30366868;STK323946;4-Nitrobenzoic acid succinimidyl ester;AKOS000497418;2,5-Dioxopyrrolidin-1-yl4-nitrobenzoate;BS-42517;CS-0320489;SR-01000203015;SR-01000203015-1;1-{[(4-nitrophenyl)carbonyl]oxy}pyrrolidine-2,5-dione

Chemical Property of 2,5-Dioxopyrrolidin-1-yl 4-nitrobenzoate

Chemical Property:

• XLogP3: 0.7
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 3
• Exact Mass: 264.03823598
• Heavy Atom Count: 19
• Complexity: 405

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CC(=O)N(C1=O)OC(=O)C2=CC=C(C=C2)[N+](=O)[O-]

Technology Process of 2,5-Dioxopyrrolidin-1-yl 4-nitrobenzoate

There total 8 articles about 2,5-Dioxopyrrolidin-1-yl 4-nitrobenzoate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 96.0%

1-hydroxy-pyrrolidine-2,5-dione (6066-82-6) + 4-nitro-benzoic acid (62-23-7) → p-nitrobenzoic acid N-hydroxysuccinimide ester (30364-58-0)

Guidance literature:

4-nitro-benzoic acid; With bis(trichloromethyl) carbonate; triethylamine; In dichloromethane; at 0 ℃;

1-hydroxy-pyrrolidine-2,5-dione; In dichloromethane; at 20 ℃; for 0.5h;

DOI:10.1080/00397910902906628

Reference yield: 90.9%

→ p-nitrobenzoic acid N-hydroxysuccinimide ester (30364-58-0)

Guidance literature:

Reference yield: 82.0%

1-hydroxy-pyrrolidine-2,5-dione (6066-82-6) + 4-nitrobenzyl chloride (619-73-8) → p-nitrobenzoic acid N-hydroxysuccinimide ester (30364-58-0)

Guidance literature:

With [bis(acetoxy)iodo]benzene; In ethyl acetate; for 0.5h; cooling;

DOI:10.1246/cl.2006.566

upstream raw materials:

1-hydroxy-pyrrolidine-2,5-dione

4-nitro-benzoyl chloride

p-nitrobenzene iodide

carbon monoxide

Downstream raw materials:

1-hydroxy-pyrrolidine-2,5-dione

4-nitrobenzanilide

4-nitro-benzoic acid-[2-(1⁽³⁾H-imidazol-4-yl)-ethylamide]

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