47690
甲脒 乙酸盐
purum, ≥98.0% (NT)
别名:
乙酸甲脒
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关于此项目
线性分子式:
HN=CHNH2 · CH3COOH
化学文摘社编号:
分子量:
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
存储类别
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
法规信息
新产品
此项目有
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