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3029-30-9

3029-30-9 Structure

3029-30-9 Structure
IdentificationBack Directory
[Name]

1,4-DICYANONAPHTHALENE
[CAS]

3029-30-9
[Synonyms]

1,4-Dcyanonaphthalene
1,4-DICYANONAPHTHALENE
1,4-Dicyanonaphthalene>
Naphthalin-1,4-dicarbonitril
1,4-Nphthalenedicarbonitrile
1,4-NAPHTHALENEDICARBONITRILE
NAPHTHALENE-1,4-DICARBONITRILE
NAPHTHALENE-1,4-DICARBONITRILE, 98+%
[EINECS(EC#)]

221-197-1
[Molecular Formula]

C12H6N2
[MDL Number]

MFCD03093626
[MOL File]

3029-30-9.mol
[Molecular Weight]

178.19
Chemical PropertiesBack Directory
[Melting point ]

209-211°C
[Boiling point ]

401.2±28.0 °C(Predicted)
[density ]

1.23±0.1 g/cm3(Predicted)
[form ]

powder to crystal
[color ]

White to Orange to Green
[BRN ]

1870226
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Danger
[Hazard statements ]

H302
[Precautionary statements ]

P280f
[Risk Statements ]

20/21/22-36/37/38
[Safety Statements ]

22-36/37/39
[RIDADR ]

3276
[HS Code ]

2926.90.4801
[REACH Registrations]

Active
[HazardClass ]

6.1
[PackingGroup ]

III
Hazard InformationBack Directory
[Chemical Properties]

1,4-Dicyanonaphthalene [3029-30-9], naphthalene-1,4-dicarboxylic acid dinitrile, Mr 178.18, mp 208℃, crystallizes in long, colorless needles. 1,4-Dicyanonaphthalene is produced by condensation of 1,2-phenylenediacetonitrile with glyoxal or its bisaldimines. It is used as an intermediate for the synthesis of optical brighteners and dyes from naphtholactams.
[Uses]

1,4-Dicyanonaphthalene is used in biological studies as electron transfer mechanism of nucleic acid precursors and ctDNA with protein enzymes and several fluorescence probes in both static and excited states.
[Purification Methods]

Purify it by recrystallization from EtOH (charcoal), m 208o, and sublime it in vacuo. [Bradbrook & Linstead J Chem Soc 1742 1936, Beilstein 9 H 917, 9 II 651, 9 III 464.]
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