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Cobaltate(1-), bis(2-(2-(2-(hydroxy-kappaO)-4-nitrophenyl)diazenyl-kappaN1)-1-naphthalenolato(2-)-kappaO)-, hydrogen (1:1)

HCID 165479
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Basic informationNames & identifiersPropertiesChemistry & industryRelated reactionsCompound notes
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Basic information

CAS
15525-22-1
Standard SMILES
O=C1C=C(N([O-])[O-])C=CC1=NN=C1C=Cc2ccccc2C1=O.O=[N+]([O-])c1ccc(N=Nc2ccc3ccccc3c2[O-])c([O-])c1.[Co+3].[H+]
InChIKey
FFZRIEBZVKXFBO-QIKYXUGXSA-M
Molecular formula
C32H19CoN6O8
Average molar mass
674.5 g/mol

Names & identifiers

Preferred name
Cobaltate(1-), bis(2-(2-(2-(hydroxy-kappaO)-4-nitrophenyl)diazenyl-kappaN1)-1-naphthalenolato(2-)-kappaO)-, hydrogen (1:1)
IUPAC
cobalt(3+);2-[[4-(dioxidoamino)-6-oxocyclohexa-2,4-dien-1-ylidene]hydrazinylidene]naphthalen-1-one;hydron;2-[(4-nitro-2-oxidophenyl)diazenyl]naphthalen-1-olate
English name
C.I. Solvent Violet 1
Molecular formula
C32H19CoN6O8
Molecular weight
674.46186

Names & synonyms

15525-22-1EINECS 229-171-16421-64-3Cobaltate(1-), bis(2-((2-(hydroxy-kappaO)-4-nitrophenyl)azo-kappaN1)-1-naphthalenolato(2-)-kappaO)-, hydrogenCobaltate(1-), bis(2-(2-(2-(hydroxy-kappaO)-4-nitrophenyl)diazenyl-kappaN1)-1-naphthalenolato(2-)-kappaO)-, hydrogen (1:1)Cobaltate(1-), bis[2-[2-[2-(hydroxy-kappaO)-4-nitrophenyl]diazenyl-kappaN1]-1-naphthalenolato(2-)-kappaO]-, hydrogen (1:1)RefChem:578040605-003-6Cobaltate(1-), bis[2-[2-[2-(hydroxy-.kappa.O)-4-nitrophenyl]diazenyl-.kappa.N1]-1-naphthalenolato(2-)-.kappa.O]-, hydrogen (1:1)Hydrogen bis(2-((2-hydroxy-4-nitrophenyl)azo)naphthalen-1-olato(2-))cobaltate(1-)cobalt(3+);2-[[4-(dioxidoamino)-6-oxocyclohexa-2,4-dien-1-ylidene]hydrazinylidene]naphthalen-1-one;hydron;2-[(4-nitro-2-oxidophenyl)diazenyl]naphthalen-1-olateSolvent Violet 1
Show more names
C.I. Solvent Violet 1C.I.Solvent Violet 1:C.I.12196cobalt(3+),2-[[4-(dioxidoamino)-6-oxocyclohexa-2,4-dien-1-ylidene]hydrazinylidene]naphthalen-1-one,hydron,2-[(4-nitro-2-oxidophenyl)diazenyl]naphthalen-1-olate

Properties

Computed structural properties

Topological polar surface area
225 Ų
Hydrogen bond donors
1
Hydrogen bond acceptors
13
Rotatable bonds
3
Heavy atoms
47
Formal charge
0
Complexity
453

Chemistry & industry

Uses & manufacturing

General Manufacturing InformationCobaltate(1-), bis[2-[2-[2-(hydroxy-.kappa.O)-4-nitrophenyl]diazenyl-.kappa.N1]-1-naphthalenolato(2-)-.kappa.O]-, hydrogen (1:1): ACTIVE

Preparation methods

Preparation2-Amino-5-nitrophenol diazotization, and Naphthalen-2-ol coupling, and then into cobalt complex (1 atomic cobalt on 2 Moore single azo dye).

Upstream & downstream products

Upstream raw materials

2-Amino-5-nitrophenol2-Naphthol

Related reactions

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Compound notes

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On this pageBasic informationNames & identifiersPropertiesChemistry & industryRelated reactionsCompound notes

Database identifiers

CAS
15525-22-1、6421-64-3
PubChem CID
165479
EC Number
229-171-1、605-003-6