Basic information
- CAS
7316-92-9- Standard SMILES
N=C(N)N=Nc1ccc(O)cc1- InChIKey
SONVVDBBKOJLQF-UHFFFAOYSA-N- Molecular formula
- C7H8N4O
- Average molar mass
- 164.16 g/mol
- Monoisotopic mass
- 164.06981089
Names & identifiers
- Preferred name
- 3-(4-Oxocyclohexa-2,5-dien-1-ylidene)carbazamidine
- IUPAC
- 1-(4-hydroxyphenyl)iminoguanidine
- English name
- 3-(4-oxocyclohexa-2,5-dien-1-ylidene)carbazamidine
- Molecular formula
- C7H8N4O
- Molecular weight
- 164.16
Names & synonyms
7316-92-93-(4-Oxocyclohexa-2,5-dien-1-ylidene)carbazamidine1-(4-hydroxyphenyl)iminoguanidineNSC3786471,4-Benzoquinone MonoguanylhydrazoneNSC-378647Hydrazinecarboximidamide,2-(4-oxo-2,5-cyclohexadien-1-ylidene)-2-[(4-oxocyclohexa-2,5-dien-1-ylidene)amino]guanidineEINECS 230-781-5Ambazone Impurity 1NSC 37864784DCC7NFH3
Show more names
Ambazone Impurity1-Amidino-2-(4-oxo-2,5-cyclohexadien-1-ylidene)hydrazineHydrazinecarboximidamide, 2-(4-oxo-2,5-cyclohexadien-1-ylidene)-
Benzochinon-monoguanylhydrazonSCHEMBL6277905DTXSID40223413GDFOKRDMGTXXCS-UHFFFAOYSA-NHMS1681B02AKOS000622837AKOS003295486ST085817
Database identifiers
- CAS
7316-92-9- PubChem CID
- 72789
- DTXSID
DTXSID40223413- UNII
- 84DCC7NFH3
- EC Number
- 230-781-5
Properties
Computed structural properties
- XLogP
- 1.1
- Topological polar surface area
- 94.8 Ų
- Hydrogen bond donors
- 3
- Hydrogen bond acceptors
- 3
- Rotatable bonds
- 2
- Heavy atoms
- 12
- Formal charge
- 0
- Complexity
- 184
Physicochemical properties
- FDA UNII
- 84 DCC7NFH3 · 84DCC7NFH3
Chemistry & industry
Applications
Uses1,4-Benzoquinone monoguanylhydrazone is a hydrazone derivative of p-Benzoquinone (B206580), an aromatic compound that is used to couple antigens and antibodies to marker substances such as erythrocytes. 1,4-Benzoquinone monoguanylhydrazone also exhibits potential antineoplastic activity.
Suppliers3 total
陕西缔都新材料有限公司029-63373950 17392216152 · [email protected]
孟成科技（上海）有限公司400-820-6829 · [email protected]
上海择睿生物科技有限公司021-54580889 18321124657 · [email protected]
Related reactions
0 records
No reaction records under the current filter.
Compound notes
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