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Dokumente

S9381

Sigma-Aldrich

Succinimid

Synonym(e):

2,5-Pyrrolidin-dion

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About This Item

Empirische Formel (Hill-System):
C4H5NO2
CAS-Nummer:
123-56-8
Molekulargewicht:
99.09
Beilstein:
108440
EG-Nummer:
204-635-6
MDL-Nummer:
MFCD00005495
UNSPSC-Code:
12352209
PubChem Substanz-ID:
24899836

Assay

99.1%

Qualitätsniveau

200

Form

powder or crystals

Farbe

white to off-white

bp

285-290 °C (lit.)

mp (Schmelzpunkt)

123-125 °C (lit.)

SMILES String

O=C1CCC(=O)N1

InChI

1S/C4H5NO2/c6-3-1-2-4(7)5-3/h1-2H2,(H,5,6,7)

InChIKey

KZNICNPSHKQLFF-UHFFFAOYSA-N

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Verwandte Kategorien

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 1

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Analysenzertifikate (COA)

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Norbormide [5-(alpha-hydroxy-alpha-2-pyridylbenzyl)-7-(alpha-2-pyridylbenzylidene)-5-norbornene-2,3-dicarboximide] (NRB, 1), an existing but infrequently used rodenticide, is known to be uniquely toxic to rats but relatively harmless to other rodents and mammals. A series of NRB-related analogues were prepared to investigate the structural features responsible for
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We have developed a scaffold material consisting of a covalently-bonded structure of alginate and atelocollagen (AtCol). Addition of calcium ions caused the material to form a hydrogel (alginate-modified AtCol gel). The condition of the alginate-modified AtCol gel could be controlled
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Journal of pharmaceutical and biomedical analysis, 72, 65-73 (2012-11-14)
Reversed-phase thin-layer chromatographic (RP TLC) retention coefficients for a newly designed series of N-phenyl-3-methyl succinimide derivatives, of a rationally expected anticonvusant activity, were determined as parameters of their lipophilicity. Basic pharmacokinetic descriptors of the agents were calculated in silico with
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Rapid in-field diagnosis is very important to prevent the outbreak of various infectious and contagious diseases. Highly sensitive and quantitative detection of diseases can be performed using fluorescent immunochemical assay with specific antigen-antibody binding and a good quality fluorophore. This
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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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