CAS 1128-13-8

Formula: C6H8N4O2

InChI: InChI=1S/C6H8N4O2/c7-1-2(8)6(12)4(10)3(9)5(1)11/h7-10H2

InChI key: DNHCPEFCQYRQQN-UHFFFAOYSA-N

SMILES: C1(=C(C(=O)C(=C(C1=O)N)N)N)N

2,3,5,6-Tetraaminocyclohexa-2,5-diene-1,4-dione

CAS: 1128-13-8

Formula: C₆H₈N₄O₂

Purity: >95.0%(T)

Color and Shape: Blue to Dark purple to Dark blue powder to crystal

Molecular weight: 168.16

Ref: 3B-T4344

2,3,5,6-tetraaminocyclohexa-2,5-diene-1,4-dione

CAS: 1128-13-8

2,3,5,6-tetraaminocyclohexa-2,5-diene-1,4-dione

Formula: C₆H₈N₄O₂

Purity: 98%

Molecular weight: 168.15

Ref: 54-OR76369

2,3,5,6-tetraaminocyclohexa-2,5-diene-1,4-dione

CAS: 1128-13-8

Formula: C₆H₈N₄O₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 168.1533

Ref: IN-DA0081S4

2,3,5,6-Tetraaminobenzoquinone

CAS: 1128-13-8

2,3,5,6-Tetraaminobenzoquinone

Formula: C₆H₈N₄O₂

Purity: 97%

Molecular weight: 168.15

Ref: IN-DG01317144

2,3,5,6-tetraaminocyclohexa-2,5-diene-1,4-dione

CAS: 1128-13-8

Purity: 97%

Color and Shape: Solid

Molecular weight: 168.1560059

Ref: 10-F693777

2,3,5,6-Tetraaminocyclohexa-2,5-diene-1,4-dione

CAS: 1128-13-8

Tetraaminocyclohexa-2,5-diene-1,4-dione is a molecule that is acidic and has functional groups. Tetraaminocyclohexa-2,5-diene-1,4-dione is a diazonium salt that can be systematically synthesized from the corresponding aromatic amine. The nature of protonated tetraaminocyclohexa-2,5-diene-1,4-dione and its anion radical are acceptors in devices that use light to activate them. Tetraaminocyclohexa-2,5-diene-1,4-dione also has high densities and activation energies. Tetraaminocyclohexa-2,5-diene -1,4 -dione can be used as a rechargeable battery material because it can be reversibly oxidized or reduced.

Formula: C₆H₈N₄O₂

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 168.15 g/mol

Ref: 3D-BAA12813