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Merck
모든 사진(1)

주요 문서

S5553

Sigma-Aldrich

Succinimide

98%

동의어(들):

2,5-Pyrrolidinedione

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About This Item

실험식(Hill 표기법):
C4H5NO2
CAS Number:
Molecular Weight:
99.09
Beilstein:
108440
EC Number:
MDL number:
UNSPSC 코드:
12352103

분석

98%

bp

285-290 °C (lit.)

mp

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)

InChI key

KZNICNPSHKQLFF-UHFFFAOYSA-N

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제품 번호
설명
가격

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

개인 보호 장비

Eyeshields, Gloves, type N95 (US)


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문서 라이브러리 방문

Mathias Q Müller et al.
Journal of mass spectrometry : JMS, 45(8), 880-891 (2010-07-08)
The fragmentation behavior of a novel thiourea-based cross-linker molecule specifically designed for collision-induced dissociation (CID) MS/MS experiments is described. The development of this cross-linker is part of our ongoing efforts to synthesize novel reagents, which create either characteristic fragment ions
Wataru Kamimura et al.
Journal of biomaterials science. Polymer edition, 23(5), 609-628 (2011-02-12)
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
Zhiwei Lin et al.
Physical chemistry chemical physics : PCCP, 14(30), 10445-10454 (2012-05-05)
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
Srinivasa Reddy Mothe et al.
The Journal of organic chemistry, 76(8), 2521-2531 (2011-03-15)
A one-pot, two-step method to prepare 3-halohydrofurans efficiently by TfOH-catalyzed hydroxylation/halocyclization of cyclopropyl methanols with H(2)O and N-halosuccinimide (NXS, X=1, Br, Cl) or Selectfluor is described. The reactions proceed rapidly under mild and operationally straightforward conditions with a catalyst loading
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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