6684-16-8

Basic information

• Product Name: N-(2-CHLORO-3-PHENYLIMINO-1-PROPEN-1-YL)-ANILINE HYDROCHLORIDE
• Synonyms: N-(2-CHLORO-3-PHENYLIMINO-1-PROPEN-1-YL)-ANILINE HYDROCHLORIDE;N-(2-CHLORO-3-PHENYLIMINO-1-PROPENYL)ANILINE HYDROCHLORIDE;N-(2-Chloro-3-phenylimino-1-propen-1-yl)-anilineHCl;N-[2-Chloro-3-(phenylamino)-2-propen-1-ylidene]-benzenamine hydrochloride (1:1)
• CAS NO: 6684-16-8
• Molecular Formula: C₁₅H₁₃ClN₂*ClH
• Molecular Weight: 293.19
• Mol File: 6684-16-8.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-(2-CHLORO-3-PHENYLIMINO-1-PROPEN-1-YL)-ANILINE HYDROCHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-CHLORO-3-PHENYLIMINO-1-PROPEN-1-YL)-ANILINE HYDROCHLORIDE(6684-16-8)
• EPA Substance Registry System: N-(2-CHLORO-3-PHENYLIMINO-1-PROPEN-1-YL)-ANILINE HYDROCHLORIDE(6684-16-8)

Safety Data

• Hazardous Substances Data: 6684-16-8(Hazardous Substances Data)

Upstream product

• 766-40-5 Mucochloric acid 
• 62-53-3 aniline 
• 57697-64-0 mucochloric acid 
• 142-04-1 aniline hydrochloride 
• 87-56-9 mucochloric acid 

Downstream Products

• 119569-97-0 MHI-106 
• 119569-97-0 2-((1E,3Z,5E)-3-chloro-5-(1,3,3-trimethylindolin-2-ylidene)penta-1,3-dien-1-yl)-1,3,3-trimethyl-3H-indol-1-ium iodide 

Relevant articles and documents

COMPOUNDS FOR PHOTODYNAMIC THERAPY AND RELATED USES

Disclosed herein are symmetrical and unsymmetrical carbocyanine dyes. Irradiation of the dyes generates reactive species which contribute to DNA damage. The dyes are useful for the treatment of various cancers and cell growth disorders.

Polymethine Thiopyrylium Fluorophores with Absorption beyond 1000 nm for Biological Imaging in the Second Near-Infrared Subwindow

Small-molecule fluorescence imaging in the second near-infrared (NIR-II, 1000-1700 nm) window has gained increasing interest in clinical application. Till now, very few studies have been exploited in the small-molecule fluorophores with both excitation and emission in the NIR-II window. Inspired by the indocyanine green structure, a series of polymethine dyes with both absorption and emission in the NIR-II window have been developed for NIR-II imaging, providing the feasibility to directly compare optical imaging in the NIR-IIa (1300-1400 nm) subwindow under 1064 nm excitation with that in the NIR-II window under 808 nm excitation. The signal-background ratio and the tumor-normal tissue ratio achieved great improvement under 1064 nm excitation in the imaging of mouse blood pool and U87 glioma tumors. Our study not only introduces a broadband emission fluorophore for both NIR-II and NIR-IIa imaging, but also reveals the advantages of NIR-II excitation over NIR-I in in vivo imaging.

Near-Infrared Illumination of Native Tissues for Image-Guided Surgery

Our initial efforts to prepare tissue-specific near-infrared (NIR) fluorescent compounds generated successful correlation between physicochemical properties and global uptake in major organs after systemic circulation and biodistribution. Herein, we focus on the effects on biodistribution based on modulating electronic influencing moieties from donating to withdrawing moieties at both the heterocyclic site and through meso-substitution of pentamethine cyanine fluorophores. These selected modifications harnessed innate biodistribution pathways through the structure-inherent targeting, resulting in effective imaging of the adrenal glands, pituitary gland, lymph nodes, pancreas, and thyroid and salivary glands. These native-tissue contrast agents will arm surgeons with a powerful and versatile arsenal for intraoperative NIR imaging in real time.