28280
Cyanoacetamide
purum, ≥98.0% (GC)
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About This Item
Linear Formula:
NCCH2CONH2
CAS Number:
Molecular Weight:
84.08
EC Number:
203-531-8
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
878221
MDL number:
grade
purum
assay
≥98.0% (GC)
mp
119-121 °C (lit.), 120-122 °C
SMILES string
NC(=O)CC#N
InChI
1S/C3H4N2O/c4-2-1-3(5)6/h1H2,(H2,5,6)
InChI key
DGJMPUGMZIKDRO-UHFFFAOYSA-N
Other Notes
Reagent for the analysis of uronic acids by HPLC; For the spectrofluorimetric determination of catecholamines
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
419.0 °F - closed cup
flash_point_c
215 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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S. Honda et al.
Analytica Chimica Acta, 149, 297-297 (1983)
S Honda et al.
Analytical biochemistry, 134(1), 34-39 (1983-10-01)
A convenient method for the rapid and sensitive automated analysis of uronic acids, based on high-performance anion-exchange chromatography on a Hitachi 2633 column and photometric as well as fluorimetric postcolumn labeling with 2-cyanoacetamide, has been developed. This method allows the
Kan Wang et al.
Journal of combinatorial chemistry, 11(5), 920-927 (2009-08-22)
Cyanoacetic acid derivatives are the starting materials for a plethora of multicomponent reaction (MCR) scaffolds. However the diversity of these scaffolds is hampered by the low variability of the cyanoacetic acid derivatives in the past. Here we describe valuable protocols
Xiaofei Zeng et al.
Organic letters, 12(10), 2414-2417 (2010-05-01)
A clean and highly efficient enantioselective addition of alpha-isocyanoacetamides to aliphatic aldehydes catalyzed by chiral phosphoric acid in the presence of MS 5 A in toluene at -40 degrees C was developed. Excellent yields (85-98%) and good to excellent enantioselectivities
M Rizk et al.
Farmaco (Societa chimica italiana : 1989), 54(1-2), 47-50 (1999-05-13)
A highly sensitive and specific fluorimetric method was developed for the determination of oxamniquine in biological fluids (urine and plasma). The proposed method is based on the reduction of oxamniquine using zinc/calcium chloride to obtain its nitroso derivative. The latter
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