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2,5-Dioxopyrrolidin-1-yl methylcarbamate

Base Information Edit
  • Chemical Name:2,5-Dioxopyrrolidin-1-yl methylcarbamate
  • CAS No.:18342-66-0
  • Molecular Formula:C6H8N2O4
  • Molecular Weight:172.141
  • Hs Code.:2925190090
  • European Community (EC) Number:629-302-6
  • DSSTox Substance ID:DTXSID00402666
  • Nikkaji Number:J2.220.154I
  • Wikidata:Q27157348
  • Mol file:18342-66-0.mol
2,5-Dioxopyrrolidin-1-yl methylcarbamate

Synonyms:18342-66-0;2,5-Dioxopyrrolidin-1-yl methylcarbamate;N-Succinimidyl N-methylcarbamate;(2,5-dioxopyrrolidin-1-yl) N-methylcarbamate;N-Succinimdyl-N-methylcarbamate;MFCD00800292;1-[(methylcarbamoyl)oxy]pyrrolidine-2,5-dione;MIC substitute;Methyl isocyanate substitute;2,5-Pyrrolidinedione, 1-[[(methylamino)carbonyl]oxy]-;N-Succinimidyl Methylcarbamate;SCHEMBL352074;CHEBI:83949;DTXSID00402666;XMNGSPOWUCNRMO-UHFFFAOYSA-N;Methylcarbamic acid succinimidyl ester;AKOS016005526;AC-4863;CS-W008138;AS-13518;SY066862;2,5-dioxopyrrolidin-1-yl N-methylcarbamate;FT-0650761;U0108;A812775;N-Succinimidyl N-methylcarbamate, >=97.0% (N);J-011744;Methyl-carbamic acid 2,5-dioxo-pyrrolidin-1-yl ester;Q27157348;N-methylcarbamic acid (2,5-dioxo-1-pyrrolidinyl) ester;[2,5-bis(oxidanylidene)pyrrolidin-1-yl] N-methylcarbamate

Suppliers and Price of 2,5-Dioxopyrrolidin-1-yl methylcarbamate
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Usbiological
  • N-Succinimidyl N-Methylcarbamate
  • 500mg
  • $ 319.00
  • TRC
  • N-Succinimidyl N-methylcarbamate
  • 2.5g
  • $ 130.00
  • TCI Chemical
  • N-Succinimidyl Methylcarbamate >98.0%(N)
  • 1g
  • $ 23.00
  • TCI Chemical
  • N-Succinimidyl Methylcarbamate >98.0%(N)
  • 5g
  • $ 64.00
  • Sigma-Aldrich
  • N-Succinimidyl N-methylcarbamate ≥97.0% (N)
  • 5g
  • $ 173.00
  • Sigma-Aldrich
  • N-Succinimidyl N-methylcarbamate ≥97.0% (N)
  • 25g
  • $ 734.00
  • Crysdot
  • 2,5-Dioxopyrrolidin-1-ylmethylcarbamate 97%
  • 100g
  • $ 396.00
  • Chemenu
  • 2,5-Dioxopyrrolidin-1-ylmethylcarbamate 97%
  • 25g
  • $ 153.00
  • Chemenu
  • 2,5-Dioxopyrrolidin-1-ylmethylcarbamate 97%
  • 100g
  • $ 374.00
  • Ark Pharm
  • 2,5-Dioxopyrrolidin-1-yl methylcarbamate 97%
  • 100g
  • $ 432.00
Total 62 raw suppliers
Chemical Property of 2,5-Dioxopyrrolidin-1-yl methylcarbamate Edit
Chemical Property:
  • Melting Point:148-153 °C 
  • Refractive Index:1.527 
  • PKA:11.00±0.46(Predicted) 
  • PSA:75.71000 
  • Density:1.416 g/cm3 
  • LogP:-0.26480 
  • Storage Temp.:2-8°C 
  • Sensitive.:Moisture Sensitive 
  • Solubility.:Dichloromethane (Slightly), DMSO (Slightly) 
  • Water Solubility.:Slightly soluble in water. 
  • XLogP3:-0.9
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:2
  • Exact Mass:172.04840674
  • Heavy Atom Count:12
  • Complexity:222
Purity/Quality:

99% *data from raw suppliers

N-Succinimidyl N-Methylcarbamate *data from reagent suppliers

Safty Information:
  • Pictogram(s): IrritantXi 
  • Hazard Codes:Xi 
  • Statements: 36/37/38 
  • Safety Statements: 26-36 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CNC(=O)ON1C(=O)CCC1=O
  • Uses N-Succinimidyl N-Methylcarbamate is used as a reagent in the synthesis of Argifin, a natural product chitinase inhibitor with chemotherapeutic potential. N-Succinimidyl N-Methylcarbamate is also used as a reagent in the preparation of 5-Amino-N1-methyl-1H-imidazole-1,4-dicarboxamide (A616300); a metabolite of Temozolomide (T017775) which is an imidazotetrazine alkylating agent and antineoplastic.
Technology Process of 2,5-Dioxopyrrolidin-1-yl methylcarbamate

There total 4 articles about 2,5-Dioxopyrrolidin-1-yl methylcarbamate 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:
Guidance literature:
With triethylamine; In ethyl acetate; at 0 - 20 ℃; for 24h;
DOI:10.1016/j.ejmech.2014.05.032
Guidance literature:
With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 - 3 ℃; for 48h;
DOI:10.1055/s-1993-25809
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