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2,5-Pyrrolidinedione, 1-[3-(methyldithio)-1-oxopropoxy]-

Base Information Edit
  • Chemical Name:2,5-Pyrrolidinedione, 1-[3-(methyldithio)-1-oxopropoxy]-
  • CAS No.:403518-14-9
  • Molecular Formula:C8H11NO4S2
  • Molecular Weight:249.312
  • Hs Code.:
  • Mol file:403518-14-9.mol
2,5-Pyrrolidinedione, 1-[3-(methyldithio)-1-oxopropoxy]-

Synonyms:3-methyldisulfanylpropionic acid 2,5-dioxopyrrolidin-1-yl ester;

Suppliers and Price of 2,5-Pyrrolidinedione, 1-[3-(methyldithio)-1-oxopropoxy]-
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
  • 1-[3-(Methyldithio)-1-oxopropoxy]-2,5-pyrrolidinedione
  • 100mg
  • $ 170.00
  • TRC
  • 1-[3-(Methyldithio)-1-oxopropoxy]-2,5-pyrrolidinedione
  • 1g
  • $ 1280.00
  • Absolute Chiral
  • 2,5-dioxopyrrolidin-1-yl3-(methyldisulfanyl)propanoate techgrade
  • 100 mg
  • $ 298.00
Total 0 raw suppliers
Chemical Property of 2,5-Pyrrolidinedione, 1-[3-(methyldithio)-1-oxopropoxy]- Edit
Chemical Property:
  • PSA:114.28000 
  • LogP:0.93280 
Purity/Quality:

1-[3-(Methyldithio)-1-oxopropoxy]-2,5-pyrrolidinedione *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Uses 1-[3-(Methyldithio)-1-oxopropoxy]-2,5-pyrrolidinedione is an intermediate used in the synthesis of Mertansine-13CD3 (M257802), which is the isotope labelled analog of Mertansine (M257800); a cytotoxic agent used as the cytotoxic component in antibody-drug conjugates.
Technology Process of 2,5-Pyrrolidinedione, 1-[3-(methyldithio)-1-oxopropoxy]-

There total 1 articles about 2,5-Pyrrolidinedione, 1-[3-(methyldithio)-1-oxopropoxy]- 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 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; for 2h;
DOI:10.1021/jm060319f
Guidance literature:
In aq. phosphate buffer; acetonitrile; at 20 ℃; for 48h; pH=7.5;
DOI:10.1039/c6ob01751g
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