2642-98-0

Basic information

• Product Name: 6-AMINOCHRYSENE
• Synonyms: ADCA;6-Amc;Chrysenex;Chrysonex;6-CHRYSENAMINE;6-AMINOCHRYSENE;AMINOCHRYSENE;AMINOCHRYSENE, 6-
• CAS NO: 2642-98-0
• Molecular Formula: C₁₈H₁₃N
• Molecular Weight: 243.3
• EINECS: 220-149-7
• Mol File: 2642-98-0.mol
• Article Data: 8

Chemical Properties

• Melting Point: 209-211 °C(lit.)
• Boiling Point: 376.18°C (rough estimate)
• Flash Point: 286.9°C
• Appearance: /
• Density: 0.8933 (rough estimate)
• Vapor Pressure: 3.56E-10mmHg at 25°C
• Refractive Index: 1.4500 (estimate)
• Storage Temp.: 2-8°C
• Solubility: Acetone (Slightly), Chloroform (Slightly), Methanol (Slightly, Heated)
• PKA: 4.32±0.30(Predicted)
• Water Solubility: 155ug/L(24 oC)
• Merck: 13,2275
• CAS DataBase Reference: 6-AMINOCHRYSENE(CAS DataBase Reference)
• NIST Chemistry Reference: 6-AMINOCHRYSENE(2642-98-0)
• EPA Substance Registry System: 6-AMINOCHRYSENE(2642-98-0)

Safety Data

• Hazard Codes: Xn
• Statements: 22
• Safety Statements: 45-36/37/39-26
• WGK Germany: 3
• RTECS: GC0500000
• Hazardous Substances Data: 2642-98-0(Hazardous Substances Data)

Usage

Chemical Properties

ORANGE TO BROWN CRYSTALLINE POWDER

Uses

Different sources of media describe the Uses of 2642-98-0 differently. You can refer to the following data:
1. Produces tumors in mice.
2. 6-Aminochrysene is a potent inhibitor of transferase activity. Also, it is used for the synthesis of diarylthiourea analogs as novel anti-cancer agents.

InChI:InChI=1/C18H13N/c19-18-11-17-13-6-2-1-5-12(13)9-10-15(17)14-7-3-4-8-16(14)18/h1-11H,19H2

Upstream product

• 218-01-9 chrysene 
• 7647-01-0 hydrogenchloride 
• 7496-02-8 6-nitrochrysene 
• 64-19-7 acetic acid 
• 10034-85-2 hydrogen iodide 

Downstream Products

• 196-79-2 Benzonaphtho<1,2-f>chinolin 
• 625457-62-7 4-{4-[2-(bis-ethylsulfanyl-methyl)-pyrrolidine-1-carbonyl]-2-methoxy-5-nitro-phenoxy}-N-chrysen-6-yl-butyramide 
• 625457-63-8 5-{4-[(S)-2-(Bis-ethylsulfanyl-methyl)-pyrrolidine-1-carbonyl]-2-methoxy-5-nitro-phenoxy}-pentanoic acid chrysen-6-ylamide 
• 854849-81-3 C₂₆H₁₉NO 
• 1224702-75-3 4β-(6''-chrycenylamino)-4-desoxypodophyllotoxin 
• 1224702-81-1 4'-O-demethyl-4β-(1''-chrycenylamino)-4-desoxypodophyllotoxin 
• 63018-97-3 6-Acetylaminochrysen 
• 7499-59-4 6-acetoxychrysene 

Relevant articles and documents

Chrysene-Based Azahelicene π-Linker of D-π-D-Type Hole-Transporting Materials for Perovskite Solar Cells

Chrysene is a readily available material for exploring new polycyclic aromatic hydrocarbons (PAHs). In this study, two chrysene based azahelicenes, nine-membered BA7 and ten-membered DA6, are constructed by intermolecular oxidative annulation of 6-aminochrysene and intramolecular annulation of N6,N12-bis(1-chloronaphthalen-2-yl)chrysene-6,12-diamine, respectively. The hexylated BA7 and DA6 and their brominated products were undoubtedly characterized by single crystal XRD. Subsequent amination with bis(9-methyl-9H-carbazol-3-yl)amine (BMCA) electron donor afforded D-π-D-type semiconductors BA7-BMCA and DA6-BMCA with beneficial properties to act as hole transport materials for perovskite solar cell. Compared with 19.4 % champion power conversion efficiency (PCE) of BA7-BMCA based device, a higher PCE of 20.2 % for DA6-BMCA counterpart may be attributed to its S-shaped double helicene-like linker with extended π-conjugated system.

Design and synthesis of novel chrysene-linked pyrrolo[2,1-c][1,4]-benzodiazepine hybrids as potential DNA-binding agents

Chrysene-linked pyrrolobenzodiazepine hybrids have been prepared that posses cytotoxicity in some cancer cell lines. They also exhibit promising DNA-binding affinity and this is supported by molecular modeling studies.

Ultrasound-promoted highly efficient reduction of aromatic nitro compounds to the aromatic amines by samarium/ammonium chloride

Ultrasound-promoted, highly efficient reduction of several aromatic nitro compounds to the aromatic amines was achieved by samarium/ammonium chloride mediated reaction. (C) 2000 Elsevier Science Ltd.