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About This Item
Empirical Formula (Hill Notation):
C5H6N2O2
CAS Number:
Molecular Weight:
126.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
222-046-2
Beilstein/REAXYS Number:
114435
MDL number:
Assay:
98%
Form:
solid
Quality Level
assay
98%
form
solid
mp
77-79 °C (lit.)
functional group
amine, hydrazine
SMILES string
NNC(=O)c1ccco1
InChI
1S/C5H6N2O2/c6-7-5(8)4-2-1-3-9-4/h1-3H,6H2,(H,7,8)
InChI key
SKTSVWWOAIAIKI-UHFFFAOYSA-N
Application
2-Furoic hydrazide (2-Furoylhydrazine) was used to study the Fourier transform infrared spectra, 1H NMR and 13C NMR spectra. It was also used as a reagent for determination of carbohydrates.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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V Vimalraj et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 78(2), 670-675 (2010-12-31)
The Fourier transform infrared spectra, 1H NMR and 13C NMR spectra of 2-furoic hydrazide have been recorded. Optimized geometry, frequency and intensity of the vibrational bands of 2-furoic hydrazide were obtained by the density functional theory (DFT) and ab initio
M Lever et al.
Analytical biochemistry, 139(1), 205-211 (1984-05-15)
4- Hydroxybenzoylhydrazine ( PAHBAH ) reacts with glucose in hot aqueous solution when alkali exceeds aroylhydrazine concentration. The related 2- furoylhydrazine ( FAH ) reacts at lower alkali concentrations, making this an attractive alternative carbohydrate reagent since it is (unlike
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 130443-5G | 04061838727503 |