B13071
Benzhydrazide
98%
Synonym(s):
Benzoic acid hydrazide, Benzoylhydrazine
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All Photos(3)
About This Item
Linear Formula:
C6H5CONHNH2
CAS Number:
Molecular Weight:
136.15
Beilstein:
471797
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
98%
form
powder
mp
112-114 °C (lit.)
SMILES string
NNC(=O)c1ccccc1
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
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Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Carc. 2 - Skin Irrit. 2
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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
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
Liping Bai et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 214, 436-444 (2019-02-27)
A simple water-soluble polymer PEGBHB based on polyethylene glycol bearing a Schiff base derivative moiety was successfully designed and synthesized. PEGBHB showed high selectivity and sensitivity towards Al3+ as a turn-on fluorescent chemosensor without influence by other competitive metal ions
Daniel E Carvajal-Hausdorf et al.
Journal for immunotherapy of cancer, 5(1), 81-81 (2017-10-19)
Immunostimulatory therapies targeting immune-suppressive pathways produce durable responses in advanced solid tumors. Indoleamine 2,3-dioxygenase (IDO) is the rate-limiting oxidoreductase that catalyzes the degradation of tryptophan to kynurenine. IDO induces immune tolerance by downregulating CD8+ and effector CD4+ T cell responses.
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