grade
ACS reagent
Quality Level
vapor pressure
<0.001 hPa
Assay
≥97%
form
powder
solid
impurities
≤0.005% insolubles
ign. residue
≤0.01%
pH
6.7-7.3 (25 °C, 5%)
mp
110-112 °C (dec.) (lit.)
anion traces
chloride (Cl-): ≤5 ppm
nitrate (NO3-): ≤0.001%
sulfate (SO42-): ≤0.001%
cation traces
Fe: ≤5 ppm
heavy metals: ≤5 ppm
SMILES string
N.CC(O)=O
InChI
1S/C2H4O2.H3N/c1-2(3)4;/h1H3,(H,3,4);1H3
InChI key
USFZMSVCRYTOJT-UHFFFAOYSA-N
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General description
Application
- 1,3-oxazine derivatives by three-component condensation reaction with 2-naphthol and aromatic aldehydes.
- Symmetrical terpyridine derivatives by treating with aromatic aldehydes and ethyl cyanoacetate.
- Isoquinolines, furopyridines, and thienopyridines via Pd-catalyzed sequential coupling-imination-annulation reactions of ortho-bromoarylaldehydes and terminal alkynes.
It can also be used as a nitrogen source to synthesize benzoxazole derivatives via multicomponent condensation reaction with catechols, and various aldehydes in the presence of Fe(III)−salen complex as a catalyst.
Features and Benefits
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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