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376566

Sigma-Aldrich

1-Acetylguanidine

98%

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About This Item

Fórmula lineal:
CH3CONHC(=NH)NH2
Número de CAS:
5699-40-1
Peso molecular:
101.11
EC Number:
227-180-5
MDL number:
MFCD00075615
UNSPSC Code:
12352100
PubChem Substance ID:
24863452
NACRES:
NA.22

assay

98%

mp

181-183 °C (lit.)

SMILES string

CC(=O)NC(N)=N

InChI

1S/C3H7N3O/c1-2(7)6-3(4)5/h1H3,(H4,4,5,6,7)

InChI key

NGGXACLSAZXJGM-UHFFFAOYSA-N

General description

1-Acetylguanidine is a guanidine derivative.

application

1-Acetylguanidine (N-Carbamimidoylacetamide) may be used in the synthesis of 1H-imidazol-2-amine derivatives.
1-Acetylguanidine may be used in the preparation of:
  • 4-[5-(3-fluorophenyl)furan-2-yl]-2-acetylamino-5-methylimidazole
  • novel series of amino-protected 6-alkyl-, 6-aryl-, 6-heteroaryl- and 5,6-fused-cycloalkane 4-trifluoromethyl-2-acetylaminopyrimidines
  • new series of protected 6-alkyl- and 6-aryl-2-acetylamino-4(3H)-pyrimidinones
  • 4-trifluoromethyl-6-(2,2-dimethoxyethyl)-2-acetylaminopyrimidine

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Letters in Organic Chemistry, 4(7), 495-499 (2007)
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Novel thiazole derivatives were synthesized and evaluated as vascular adhesion protein-1 (VAP-1) inhibitors. Although we previously identified a compound (2) with potent VAP-1 inhibitory activity in rats, the human activity was relatively weak. Here, to improve the human VAP-1 inhibitory
One-pot synthesis of N2-aminoprotected 6-substituted and cycloalka[d] 4-trifluoromethyl-2-acetylaminopyrimidines.
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Journal of Heterocyclic Chemistry, 45(2), 483-487 (2008)
Dae-Kee Kim et al.
Journal of medicinal chemistry, 50(13), 3143-3147 (2007-06-08)
A series of 4(5)-(6-alkylpyridin-2-yl)imidazoles 13a-p, 17a, and 17b have been synthesized and evaluated for ALK5 inhibitory activity in an enzyme assay and in cell-based luciferase reporter assays. The quinoxalinyl analogue 13e inhibited ALK5 phosphorylation with an IC50 of 0.012 muM
Easy and regioselective access to dimethyl acetal-protected heterocycles and their efficient allylation reactions mediated by allylaluminum reagent.
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