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Merck
CN

B13071

Benzhydrazide

98%

Synonym(s):

Benzoic acid hydrazide, Benzoylhydrazine

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About This Item

Linear Formula:
C6H5CONHNH2
CAS Number:
Molecular Weight:
136.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-363-9
Beilstein/REAXYS Number:
471797
MDL number:
Assay:
98%
Form:
powder
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InChI

1S/C7H8N2O/c8-9-7(10)6-4-2-1-3-5-6/h1-5H,8H2,(H,9,10)

InChI key

WARCRYXKINZHGQ-UHFFFAOYSA-N

SMILES string

NNC(=O)c1ccccc1

assay

98%

form

powder

pictograms

Health hazardExclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Carc. 2 - Skin Irrit. 2

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

Storage Class

11 - Combustible Solids


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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
E Agostinelli et al.
The Biochemical journal, 324 ( Pt 2), 497-501 (1997-06-01)
A novel copper-depleted bovine serum amine oxidase (BSAO), in which about half the molecules contained the organic cofactor in the oxidized form, was prepared by adding a reductant in anaerobic conditions to the cyanide-reacted protein. The CuI-semiquinone formed in these
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
Venkataswamy Sorna et al.
Journal of medicinal chemistry, 56(23), 9496-9508 (2013-11-19)
Lysine specific demethylase 1 (LSD1) plays an important role in regulating histone lysine methylation at residues K4 and K9 on histone H3 and is an attractive therapeutic target in multiple malignancies. Here we report a structure-based virtual screen of a
Susan M Aitken et al.
The Biochemical journal, 375(Pt 3), 613-621 (2003-07-19)
Many compounds are oxidized by haem enzymes, such as peroxidases and cytochromes P450, to highly reactive intermediates that function as enzyme inactivators. To evaluate the potential of arylhydrazides as selective metabolically activated peroxidase inhibitors, the mechanism of HRPC (horseradish peroxidase

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