47690
Formamidine acetate salt
purum, ≥98.0% (NT)
Synonym(s):
Formamidinium acetate
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About This Item
Linear Formula:
HN=CHNH2 · CH3COOH
CAS Number:
Molecular Weight:
104.11
EC Number:
222-442-5
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
3563488
MDL number:
grade
purum
assay
≥98.0% (NT)
impurities
≤0.5% formamide
mp
~160 °C (dec.)
SMILES string
NC=N.CC(O)=O
InChI
1S/C2H4O2.CH4N2/c1-2(3)4;2-1-3/h1H3,(H,3,4);1H,(H3,2,3)
InChI key
XPOLVIIHTDKJRY-UHFFFAOYSA-N
signalword
Warning
hcodes
Hazard Classifications
Skin Sens. 1
Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Regulatory Information
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M K Rofouei et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 78(1), 88-95 (2010-10-15)
In this work, we will report a combined experimental and theoretical study on molecular and vibrational structure of N,N'-di(p-thiazole)formamidine (DpTF). DpTF has been synthesized and characterized by elemental analysis, FT-IR, FT-Raman, 1H NMR, 13C NMR spectroscopy and X-ray single crystal
Carole Anastasi et al.
Journal of medicinal chemistry, 47(5), 1183-1192 (2004-02-20)
New formamidine-3TC (3TC = 2',3'-dideoxy-3'-thiacytidine) analogues have been synthesized through various methods, and their antiviral activities (HIV, HBV) have been evaluated in vitro. Anti-HIV-1 in acutely infected MT-4 cells and peripheral blood monocellular cells (PBMCs) showed that compounds substituted by
Krzysztof Kik et al.
Anticancer research, 29(4), 1429-1433 (2009-05-06)
In this work a comparison was made of the cytotoxicity and cellular uptake of doxorubicin (DOX) and two of its derivatives containing a formamidino group (-N=CH-N<) at the 3' position with morpholine (DOXM) or hexamethyleneimine (DOXH) ring. All tests were
Andrea Porcheddu et al.
Journal of combinatorial chemistry, 11(1), 126-130 (2008-12-05)
A focused library of formamidines having several diversity points has been prepared. The use of isocyanate resin as scavenger may offer several practical advantages over conventional procedures, such as the ease of workup and availability. The technique described herein was
Kevin M Kuhn et al.
Organic letters, 10(10), 2075-2077 (2008-04-17)
A process for the preparation of symmetric and unsymmetric imidazolinium chlorides that involves reaction of a formamidine with dichloroethane and a base (a) is described. This method makes it possible to obtain numerous imidazolinium chlorides under solvent-free reaction conditions and
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