Skip to Content
Merck
All Photos(1)

Documents

376566

Sigma-Aldrich

1-Acetylguanidine

98%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CH3CONHC(=NH)NH2
CAS Number:
Molecular Weight:
101.11
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 1

1 of 1

Bonacorso HG, et al.
Letters in Organic Chemistry, 4(7), 495-499 (2007)
Easy and regioselective access to dimethyl acetal-protected heterocycles and their efficient allylation reactions mediated by allylaluminum reagent.
Bonacorso HG, et al.
ARKIVOC (Gainesville, FL, United States), 4, 291-305 (2013)
One-pot synthesis of N2-aminoprotected 6-substituted and cycloalka[d] 4-trifluoromethyl-2-acetylaminopyrimidines.
Bonacorso HG, et al.
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
Takayuki Inoue et al.
Bioorganic & medicinal chemistry, 21(13), 3873-3881 (2013-05-15)
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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service