139327
3-Nitrobenzamidine hydrochloride
95%
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About This Item
Linear Formula:
O2NC6H4C(=NH)NH2 · HCl
CAS Number:
Molecular Weight:
201.61
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
260-159-9
MDL number:
Assay:
95%
InChI key
DKNQVJWYIUJWNC-UHFFFAOYSA-N
InChI
1S/C7H7N3O2.ClH/c8-7(9)5-2-1-3-6(4-5)10(11)12;/h1-4H,(H3,8,9);1H
SMILES string
Cl.NC(=N)c1cccc(c1)[N+]([O-])=O
assay
95%
impurities
5% ammonium chloride
mp
245-248 °C (lit.)
functional group
amine, nitro
Quality Level
Related Categories
Application
3-Nitrobenzamidine hydrochloride was used as reagent during the synthesis of (Z)-3-benzoylamino-4-dimethylamino-2-oxo-3-butene.
signalword
Warning
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Gloves
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J A Raleigh et al.
Cancer clinical trials, 3(1), 55-62 (1980-01-01)
Normal tissue toxicity of nitroaromatic radiosensitizers may originate in radiosensitizer/nitroreductase interaction. A study of two mammalian cell nitroreductases, xanthine oxidase and NADH cytochrome c reductase, shows that the efficiency of electron transfer is dependent on sensitizer electron affinity and not
Transformations of (Z)-2-benzoylamino-4-dimethylamino-2-oxo-3-butene and (E)-3-benzoylamino-4-cyano-2-oxo-3-butene into pyrimidine, pyrazole and isoxazole derivatives.
Bratusek U, et al.
ARKIVOC (Gainesville, FL, United States), 77, 86-86 (2003)
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