28280
氰基乙酰胺
purum, ≥98.0% (GC)
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线性分子式:
NCCH2CONH2
化学文摘社编号:
分子量:
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
用于通过 HPLC 分析糖醛酸的试剂；用于荧光光度法测定儿茶酚胺
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
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
法规信息
新产品
此项目有
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
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
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
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