B13071
Benzhydrazide
98%
Sinonimo/i:
Benzoic acid hydrazide, Benzoylhydrazine
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About This Item
Formula condensata:
C6H5CONHNH2
Numero CAS:
Peso molecolare:
136.15
Beilstein:
471797
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Saggio
98%
Stato
powder
Punto di fusione
112-114 °C (lit.)
Stringa SMILE
NNC(=O)c1ccccc1
InChI
1S/C7H8N2O/c8-9-7(10)6-4-2-1-3-5-6/h1-5H,8H2,(H,9,10)
WARCRYXKINZHGQ-UHFFFAOYSA-N
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Categorie correlate
Avvertenze
Warning
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Acute Tox. 4 Oral - Carc. 2 - Skin Irrit. 2
Codice della classe di stoccaggio
13 - Non Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Dispositivi di protezione individuale
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
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I clienti hanno visto anche
Abd El-Aziz S Fouda et al.
Annali di chimica, 96(1-2), 85-96 (2006-06-01)
The effect of furfural benzoylhydrazone and its derivatives (I-VII) as corrosion inhibitors for C-steel in 1M phosphoric acid solution has been studied by weight-loss and galvanostatic polarization techniques. A significant decrease in the corrosion rate of C-steel was observed in
Sylvain Broussy et al.
The Journal of organic chemistry, 70(25), 10502-10510 (2005-12-06)
[reaction: see text] An isoniazid-NAD adduct has been recently proposed as the ultimate metabolite responsible for the antituberculous activity of isoniazid (INH). Its structure results from binding of the isonicotinoyl radical at C4 position of the nicotinamide ring of NAD
M Kobayashi et al.
Biochemical and biophysical research communications, 256(2), 415-418 (1999-03-18)
The amidase from Rhodococcus rhodochrous J1, which hydrolyses amide to acid and ammonia, was found to catalyze the synthesis of hydrazide using hydrazine as a substrate. This is the first report on the hydrazide synthesis through enzymatic reactions. The enzyme
S Srinivasan et al.
Journal of inorganic biochemistry, 99(3), 876-882 (2005-02-15)
Cobalt(III) complexes of the type [Co(N-N)2L](ClO4)2.H2O [where L=anionic form of para-substituted benzaldehyde-benzoylhydrazone (BHBX-); X=H, Me, OMe, OH, Cl or NO2; N-N=2,2'-bipyridine (bpy) or 1,10-phenanthroline (phen)] have been synthesized and characterized through UV-Vis, IR, NMR and electrochemical studies. The IR spectral
V Arjunan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 79(3), 486-496 (2011-05-03)
A systematic vibrational spectroscopic assignment and analysis of benzohydrazide (BH) has been carried out by using FTIR and FT-Raman spectral data. The vibrational analysis were aided by electronic structure calculations--ab initio (RHF) and hybrid density functional methods (B3LYP and B3PW91)
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