S5553
Succinimide
98%
Sinonimo/i:
2,5-Pyrrolidinedione
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About This Item
Formula empirica (notazione di Hill):
C4H5NO2
Numero CAS:
Peso molecolare:
99.09
Beilstein:
108440
Numero CE:
Numero MDL:
Codice UNSPSC:
12352103
Prodotti consigliati
Saggio
98%
P. eboll.
285-290 °C (lit.)
Punto di fusione
123-125 °C (lit.)
Stringa SMILE
O=C1CCC(=O)N1
InChI
1S/C4H5NO2/c6-3-1-2-4(7)5-3/h1-2H2,(H,5,6,7)
KZNICNPSHKQLFF-UHFFFAOYSA-N
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Sostituito da
N° Catalogo
Descrizione
Determinazione del prezzo
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 1
Dispositivi di protezione individuale
Eyeshields, Gloves, type N95 (US)
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Dual-frequency relaxation-assisted two-dimensional infrared (RA 2DIR) spectroscopy was used to investigate energy transport in polyethylene glycol (PEG) oligomers of different length, having 0, 4, 8, and 12 repeating units and end-labeled with azido and succinimide ester moieties (azPEGn). The energy
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Protein chemical degradations occur naturally into living cells as soon as proteins have been synthesized. Among these modifications, deamidation of asparagine or glutamine residues has been extensively studied, whereas the intermediate state, a succinimide derivative, was poorly investigated because of
Ohgi Takahashi et al.
Chemistry & biodiversity, 7(6), 1630-1633 (2010-06-22)
The rapid racemization of aspartic acid (Asp) residues in peptides and proteins is due mainly to the succinimide intermediate. However, there should be another mechanism for Asp racemization without intermediacy of the succinimide. The direct H-atom abstraction from the C(alpha)-atom
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