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CAS 34071-95-9

:

N-Succinimidyl 3-(4-hydroxyphenyl)propionate

Description:
N-Succinimidyl 3-(4-hydroxyphenyl)propionate, with the CAS number 34071-95-9, is a chemical compound commonly used in bioconjugation and protein labeling applications. It features a succinimidyl ester functional group, which is known for its ability to react with amine groups on proteins, facilitating the formation of stable amide bonds. The presence of the 3-(4-hydroxyphenyl)propionate moiety provides a phenolic group that can be utilized for further chemical modifications or as a reporter group in various assays. This compound is typically characterized by its solid state at room temperature and is soluble in organic solvents such as dimethyl sulfoxide (DMSO) and dimethylformamide (DMF). Its reactivity and stability make it a valuable tool in the fields of biochemistry and molecular biology, particularly in the development of targeted drug delivery systems and in the study of protein interactions. Proper handling and storage conditions are essential to maintain its integrity and reactivity.
Formula:C13H13NO5
InChI:InChI=1S/C13H13NO5/c15-10-4-1-9(2-5-10)3-8-13(18)19-14-11(16)6-7-12(14)17/h1-2,4-5,15H,3,6-8H2
InChI key:InChIKey=KYRUKRFVOACELK-UHFFFAOYSA-N
SMILES:O(C(CCC1=CC=C(O)C=C1)=O)N2C(=O)CCC2=O
Synonyms:
  • 1-{[3-(4-Hydroxyphenyl)Propanoyl]Oxy}Pyrrolidine-2,5-Dione
  • 2,5-Dioxopyrrolidin-1-yl 3-(4-hydroxyphenyl)propanoate
  • 2,5-Pyrrolidinedione, 1-[3-(4-hydroxyphenyl)-1-oxopropoxy]-
  • 3-(4-Hydroxyphenyl)propionic acid N-hydroxysuccinimide ester
  • Benzenepropanoic acid, 4-hydroxy-, 2,5-dioxo-1-pyrrolidinyl ester
  • Bolton-Hunter Reagent
  • N-Succinimidyl-3-(4-hydroxyphenyl)propionate
  • Nsc 240876
  • Succinimide, N-[(p-hydroxyhydrocinnamoyl)oxy]-
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