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4-Methyloxazolidine-2,5-dione

Base Information Edit
  • Chemical Name:4-Methyloxazolidine-2,5-dione
  • CAS No.:2224-52-4
  • Molecular Formula:C4H5NO3
  • Molecular Weight:115.089
  • Hs Code.:2934999090
  • European Community (EC) Number:250-114-1
  • NSC Number:524103
  • DSSTox Substance ID:DTXSID90922888
  • Nikkaji Number:J249.950I
  • Mol file:2224-52-4.mol
4-Methyloxazolidine-2,5-dione

Synonyms:4-Methyloxazolidine-2,5-dione;30291-41-9;1192-73-0;4-methyl-1,3-oxazolidine-2,5-dione;EINECS 214-759-2;EINECS 250-114-1;(1)-4-Methyloxazolidine-2,5-dione;2,5-oxazolidinedione, 4-methyl-;MFCD03411277;DL-Alanine-N-carboxy anhydride;4-Methyl-2,5-oxazolidinedione;Ala-NCA;NSC524103;45530-21-0;2,5-Oxazolidinedione,4-methyl-,(-)-(9CI);L-Alanine N-carboxyanhydride;SCHEMBL280456;4-methyl-oxazolidine-2,5-dione;DTXSID90922888;BCP18817;(+-)-4-methyloxazolidine-2,5-dione;AKOS016014681;FD21041;NSC-524103;SY103956;CS-0328034;FT-0689536;FT-0698196;FT-0698464;2-Hydroxy-4-methyl-1,3-oxazol-5(4H)-one;J-650094

Suppliers and Price of 4-Methyloxazolidine-2,5-dione
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
  • TRC
  • N-CarboxyalanineAnhydride
  • 250mg
  • $ 115.00
  • Crysdot
  • (S)-4-Methyloxazolidine-2,5-dione 95+%
  • 100g
  • $ 475.00
  • Chemenu
  • (S)-4-Methyloxazolidine-2,5-dione 95%
  • 5g
  • $ 92.00
  • Apolloscientific
  • (4S)-4-Methyloxazolidine-2,5-dione
  • 5g
  • $ 405.00
  • American Custom Chemicals Corporation
  • (S)-4-METHYL-2,5-OXAZOLIDINEDIONE 95.00%
  • 0.25G
  • $ 489.00
  • American Custom Chemicals Corporation
  • (S)-4-METHYL-2,5-OXAZOLIDINEDIONE 95.00%
  • 50G
  • $ 2500.69
  • Ambeed
  • (S)-4-Methyloxazolidine-2,5-dione 95%
  • 100g
  • $ 910.00
  • Ambeed
  • (S)-4-Methyloxazolidine-2,5-dione 95%
  • 25g
  • $ 276.00
  • Ambeed
  • (S)-4-Methyloxazolidine-2,5-dione 95%
  • 10g
  • $ 126.00
  • Ambeed
  • (S)-4-Methyloxazolidine-2,5-dione 95%
  • 5g
  • $ 70.00
Total 116 raw suppliers
Chemical Property of 4-Methyloxazolidine-2,5-dione Edit
Chemical Property:
  • Melting Point:92℃ 
  • Refractive Index:1.448 
  • PKA:9.38±0.40(Predicted) 
  • PSA:55.40000 
  • Density:1.296 g/cm3 
  • LogP:-0.02990 
  • Storage Temp.:Inert atmosphere,Store in freezer, under -20°C 
  • Solubility.:DMSO (Very Slightly, Heated) 
  • XLogP3:-0.1
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:0
  • Exact Mass:115.026943022
  • Heavy Atom Count:8
  • Complexity:142
Purity/Quality:

99.9% *data from raw suppliers

N-CarboxyalanineAnhydride *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1C(=O)OC(=O)N1
  • Uses (S)-4-Methyl-2,5-oxazolidonedione is a reagent used in the synthesis of poly(γ-benzyl-L-glutamate) and its block polypeptides with alanine, leucine and phenylalanine. N-Carboxyalanine Anhydride is a reagent used in the synthesis of poly(γ-benzyl-L-glutamate) and its block polypeptides with alanine, leucine and phenylalanine.
Technology Process of 4-Methyloxazolidine-2,5-dione

There total 33 articles about 4-Methyloxazolidine-2,5-dione 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 phosphorus trichloride; In dichloromethane; at 0 ℃; for 2h;
DOI:10.1016/S0040-4020(01)85371-0
Guidance literature:
With N,N-dimethyl-formamide; In dichloromethane; at 0 - 20 ℃;
DOI:10.1021/jo00212a042
Guidance literature:
With pyrographite; In tetrahydrofuran; at 55 ℃; for 1.5h;
DOI:10.1021/jo00205a039
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