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Merck

545953

Sigma-Aldrich

1-氨基海因 盐酸盐

98%

别名:

1-氨基-2,4-咪唑烷二酮 盐酸盐

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About This Item

经验公式(希尔记法):
C3H5N3O2 · HCl
CAS号:
分子量:
151.55
Beilstein:
3699376
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

98%

mp

201-205 °C (lit.)

SMILES 字串

Cl[H].NN1CC(=O)NC1=O

InChI

1S/C3H5N3O2.ClH/c4-6-1-2(7)5-3(6)8;/h1,4H2,(H,5,7,8);1H

InChI 密鑰

WEOHANUVLKERQI-UHFFFAOYSA-N

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應用

1-氨基乙内酰脲盐酸盐可作为合成 ( E )-1-(2-羟基亚苄基氨基)咪唑烷-2,4-二酮、 丹曲林 和丹曲林钠的反应物之一。

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

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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Synthesis of 1-Aminohydantoin Hydrochloride-(2-~(13) C,~(15) N_3) as Double Labeling Compound
Xu JF, et al.
Chemical World, 10, 015-015 (2012)
Crystal structure of (E)-1-(2-hydroxybenzylideneamino) imidazolidine-2, 4-dione, C10H9N3O3.
Hu, Lei, et al.
Zeitschrift fur Kristallographie, 230(2), 111-112 (2015)
Johann Leban et al.
Bioorganic & medicinal chemistry, 16(8), 4579-4588 (2008-03-04)
Peptide-semicarbazones derived from Z-Trp-Trp-Phe-aldehyde inhibit the chymotryptic activity of the human proteasome at nanomolar concentrations, but are less active in a NFkappaB reporter gene assay. Cyclic semicarbazones, in contrast, combine a strong inhibitory effect on the enzyme with an inhibition
R L White et al.
Journal of medicinal chemistry, 30(2), 263-266 (1987-02-01)
A series of 1-[[[5-(substituted phenyl)-2-oxazolyl]methylene]amino]- 2,4-imidazolidinediones (6a-t) was synthesized, and the compounds were evaluated for direct skeletal muscle inhibition in the pithed rat gastrocnemius muscle preparation. The correctness of structural assignment of the new series was verified by alternate, unequivocal
William Andrew Publishing et al.
Pharmaceutical Manufacturing Encyclopedia, 1-4, 1193-1193 (2013)

Global Trade Item Number

货号GTIN
545953-25G4061833398937
545953-5G4061832568447

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