104432-60-2

Basic information

• Product Name: Vat Orange 7
• Synonyms: C.I. 71105; 4-26-00-02613 (Beilstein Handbook Reference); BRN 0061891; Bordeaux RRN; Brilliant Orange GR; C.I. Pigment Orange 43; C.I. Vat Orange 7; CCRIS 4703; Cibanone Brilliant Orange GR; Fenanthren Brilliant Orange GR; Hostaperm Orange GR; Hostaperm Vat Orange GR; Hostavat Brilliant Orange GR; Indanthren Brilliant Orange GR; Indanthrene Brilliant Orange GR; Indanthrene Brilliant Orange GRP; IndoFast Orange OV 5983; Mikethren Brilliant Orange GR; Mikethrene Orange GR; Ostanthren Orange GR; Ostanthrene Orange GR; Palanthrene Brilliant Orange GR; Paradone Brilliant Orange GR; Paradone Brilliant Orange GR new; Pigment Scarlet 2Zh Anthraquinone VS-K; Pv Fast Orange GRL; Sanyo Permanent Orange D 213; Sanyo Permanent Orange D 616; Solanthrene Brilliant Orange JR; Symuler Fast Orange GRD; Threne Brilliant Orange GR; Tinon Brilliant Orange GR; Vat Brilliant Orange; Vat Scarlet 2Zh; trans-Perinone; Bisbenzimidazo(2,1-b:2',1'-i)benzo(lmn)(3,8)phenanthroline-8,17-dione; Vat Brilliant Orange GR; Pigment Orange 43; Bis
• CAS NO: 104432-60-2
• Molecular Formula: C₂₆H₁₂N₄O₂
• Molecular Weight: 412.3991
• EINECS: 224-597-4
• Mol File: 104432-60-2.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 927°C at 760 mmHg
• Flash Point: 514.4°C
• Density: 1.66g/cm³
• Vapor Pressure: 1.87E-35mmHg at 25°C
• Refractive Index: 1.924
• CAS DataBase Reference: Vat Orange 7(CAS DataBase Reference)
• NIST Chemistry Reference: Vat Orange 7(104432-60-2)
• EPA Substance Registry System: Vat Orange 7(104432-60-2)

Safety Data

• Hazardous Substances Data: 104432-60-2(Hazardous Substances Data)

Upstream product

• 81-30-1 1,4,5,8-naphthalenetetracarboxylic dianhydride 
• 95-54-5 1,2-diamino-benzene 
• 479-27-6 naphthalene-1,8-diamine 

Relevant articles and documents

-

-

Green and Rapid Hydrothermal Crystallization and Synthesis of Fully Conjugated Aromatic Compounds

Highly fused, fully conjugated aromatic compounds are interesting candidates for organic electronics. With higher crystallinity their electronic properties improve. It is shown here that the crystallization of three archetypes of such molecules—pentacenetetrone, indigo, and perinone—can be achieved hydrothermally. Given their molecular structure, this is a truly startling finding. In addition, it is demonstrated that perinone can also be synthesized in solely high-temperature water from the starting compounds naphthalene bisanhydride and o-phenylene diamine without the need for co-solvents or catalysts. The transformation can be drastically accelerated by the application of microwave irradiation. This is the first report on the hydrothermal generation of two fused heterocycles.

Multicyclic benzimidazole derivatives useful as photoconductive members

A compound comprising a bisbenzamidazoleperinone of the following formula wherein each of R1, R2, R3, and R4 are the same or different and are independently selected from the group consisting of hydrogen, alkyl, aryl, hydrocarbon, which may be optionally substituted or arranged in such a way as to form a cyclic ring which can be either saturated or unsaturated and halogen.