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Merck
CN

480959

羟基乙酰胺

98%

别名:

2-羟基乙酰胺

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线性分子式:
HOCH2CONH2
化学文摘社编号:
分子量:
75.07
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
98%
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InChI

1S/C2H5NO2/c3-2(5)1-4/h4H,1H2,(H2,3,5)

SMILES string

NC(=O)CO

InChI key

TZGPACAKMCUCKX-UHFFFAOYSA-N

assay

98%

mp

118-120 °C (lit.)

functional group

amide, hydroxyl

Quality Level

General description

甘氨酰胺是甘氨酸的异构体,可以通过乙醇酸乙酯的氨解来合成。已有研究报道了乙醇酰胺的构象分析。已有研究测定了其在水中的扩散系数和部分摩尔等温压缩性。人们研究了其热力学性质。人们已测得了其渗透压和活度系数。

Application

乙醇酰胺可用于制备磷酸甘油酰胺。

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Prasanta K Mohapatra et al.
Inorganic chemistry, 52(5), 2533-2541 (2013-02-12)
Diglycolamide-functionalized calix[4]arenes (C4DGAs) with varying structural modifications were evaluated for actinide complexation from their extraction behavior toward actinide ions such as UO2(2+), Pu(4+), PuO2(2+), and Am(3+) in the room temperature ionic liquid (RTIL) 1-n-octyl-3-methylimidazolium bis(trifluoromethane)sulfonamide (C8mimNTf2). The formation constants were
A Study of the Diffusion of Glycolamide in Water at 25? with the Gouy Interference Method.
Dunlop PJ and Gosting LJ.
Journal of the American Chemical Society, 75(20), 5073-5075 (1953)
R Ruhela et al.
Talanta, 85(2), 1217-1220 (2011-07-06)
A precise, sensitive and selective method for the spectrophotometric determination of palladium (II) using N,N,N',N'-tetra(2-ethylhexyl) thiodiglycolamide T(2EH)TDGA as an extractant is described. Palladium (II) forms yellow colored complex with T(2EH)TDGA which exhibits an absorption maximum at ∼ 300 nm. The
Alan C Cheng et al.
Scientific reports, 8(1), 7570-7570 (2018-05-17)
Small molecules and antibodies each have advantages and limitations as therapeutics. Here, we present for the first time to our knowledge, the structure-guided design of "chemibodies" as small molecule-antibody hybrids that offer dual recognition of a single target by both
New facile synthesis of phosphoglycolohydroxamic acid and other phosphoglycolic acid derivatives.
Weber P, et al.
Tetrahedron Letters, 44(50), 9047-9049 (2003)

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