ChemicalBook--->CAS DataBase List--->613-92-3

613-92-3

613-92-3 Structure

613-92-3 Structure
IdentificationMore
[Name]

BENZAMIDOXIME HYDROCHLORIDE
[CAS]

613-92-3
[Synonyms]

AKOS B020566
ART-CHEM-BB B020566
BENZAMIDE OXIME
BENZAMIDOXIME
BENZAMIDOXIME HYDROCHLORIDE
BUTTPARK 52\12-12
N-HYDROXY-BENZAMIDINE
N'-HYDROXYBENZENECARBOXIMIDAMIDE
RARECHEM BG FB 0126
benzohydroxamamide
n-hydroxy-benzenecarboximidamid
N'-Hydroxybenzenecarboximidamide hydrochloride
BENZAMIDOXIME 98+%
benzenylamidoxime
benzenylaminoxime
Benzenecarboxamide oxime
N2-Hydroxybenzamidine
[EINECS(EC#)]

210-361-8
[Molecular Formula]

C7H9ClN2O
[MDL Number]

MFCD06656049
[Molecular Weight]

172.61
[MOL File]

613-92-3.mol
Chemical PropertiesBack Directory
[Melting point ]

77°C
[Boiling point ]

244℃
[density ]

1.18
[Fp ]

102℃
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[solubility ]

Chloroform (Sparingly), Methanol (Slightly)
[form ]

powder to crystal
[pka]

6.85±0.69(Predicted)
[color ]

White to Almost white
[Detection Methods]

HPLC,NMR,MS
[LogP]

1.024
[CAS DataBase Reference]

613-92-3(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R23/24/25:Toxic by inhalation, in contact with skin and if swallowed .
[Safety Statements ]

S22:Do not breathe dust .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
[RIDADR ]

2811
[WGK Germany ]

3
[RTECS ]

CY6920000
[Hazard Note ]

Irritant
[HazardClass ]

IRRITANT
[HS Code ]

29242990
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Ethanol-->Sodium carbonate-->Hydroxylamine hydrochloride-->Benzonitrile
[Preparation Products]

tioxazafen-->Oxolamine-->2,4,5-Triphenylimidazole-->4-(3-phenyl-1,2,4-oxadiazol-5-yl)aniline-->Benzenecarboximidamide, N-[(4-nitrobenzoyl)oxy]--->(3-phenyl-1,2,4-oxadiazol-5-yl)methanediol
Hazard InformationBack Directory
[Chemical Properties]

White to off-white solid
[Uses]

Benzamide Oxime is used to prepare aryloxadiazoles as apoptosis inducers and anticancer agents. It is also used in the synthesis of aryloxadiazolyltropane analogs of cocaine.
[Definition]

ChEBI: A member of the class of amidoximes obtained by formal condensation of the carbonyl group of benzamide with hydroxylamine.
[Synthesis Reference(s)]

Journal of Heterocyclic Chemistry, 26, p. 125, 1989 DOI: 10.1002/jhet.5570260122
Spectrum DetailBack Directory
[Spectrum Detail]

BENZAMIDOXIME HYDROCHLORIDE(613-92-3)MS
BENZAMIDOXIME HYDROCHLORIDE(613-92-3)13CNMR
BENZAMIDOXIME HYDROCHLORIDE(613-92-3)IR1
BENZAMIDOXIME HYDROCHLORIDE(613-92-3)IR2
BENZAMIDOXIME HYDROCHLORIDE(613-92-3)Raman
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

N'-Hydroxybenzenecarboximidamide, 95%(613-92-3)
[Alfa Aesar]

Benzamidoxime, 95%(613-92-3)
[Sigma Aldrich]

613-92-3(sigmaaldrich)
[TCI AMERICA]

Benzamidoxime,>98.0%(T)(613-92-3)
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