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124753

Succinamide

Name: Succinamide
Brand: ALDRICH

98%

Synonym(s):

Succinic diamide

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About This Item

Linear Formula:

NH₂COCH₂CH₂CONH₂

CAS Number:

110-14-5

Molecular Weight:

116.12

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24847626

EC Number:

203-739-9

Beilstein/REAXYS Number:

1753983

MDL number:

MFCD00008042

Assay:

98%

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Properties

Quality Level

100

assay

98%

mp

260-265 °C (dec.) (lit.)

solubility

cold water: soluble 220 part, boiling water: soluble 9 part, alcohol: insoluble, diethyl ether: insoluble

functional group

amide

SMILES string

NC(=O)CCC(N)=O

InChI

1S/C4H8N2O2/c5-3(7)1-2-4(6)8/h1-2H2,(H2,5,7)(H2,6,8)

InChI key

SNCZNSNPXMPCGN-UHFFFAOYSA-N

Description

Application

Succinamide has been used in the characterization of a novel biuret hydrolase from the cysteine hydrolase superfamily. It was used as nitrogen supplement in the culture medium of Scenedesmus obliquus and green algae.

Storage Class

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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IR spectroscopy on jet-cooled isolated two-station rotaxanes.

Anouk M Rijs et al.

The journal of physical chemistry. A, 115(34), 9669-9675 (2011-04-29)

High-resolution IR spectroscopy has been employed to study isolated, switchable [2]rotaxanes. IR absorption spectra of two-station rotaxanes, their separate thread, and macrocycle components, as well as those of the individual stations incorporated into the thread, have been measured in the

Novel near-infrared cyanine fluorochromes: synthesis, properties, and bioconjugation.

Yuhui Lin et al.

Bioconjugate chemistry, 13(3), 605-610 (2002-05-16)

Recently, near-infrared (NIR) fluorescence light has been applied to image various biological events in vivo, because it penetrates tissue more efficiently than light in the visible spectrum. Compounds exhibiting fluorescent properties in the NIR range are key elements for this

Synthesis of novel succinamide derivatives having a 5,11-dihydro-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one skeleton as potent and selective M2 muscarinic receptor antagonists. II.

T Watanabe et al.

Chemical & pharmaceutical bulletin, 45(9), 1458-1469 (1997-10-23)

A series of succinamide derivatives containing the 5,11-dihydro-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one skeleton (6a-z) was prepared and evaluated for binding affinity to muscarinic receptors in vitro and for antagonism of bradycardia and salivation in vivo in comparison with AF-DX 116 (1a). Structure-activity relationships (SAR)

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Global Trade Item Number

SKU	GTIN
124753-100G	04061838723116