904369-20-6

Basic information

• Product Name: 7-Bromo-quinoline-2-carbaldehyde
• Synonyms: 7-Bromo-quinoline-2-carbaldehyde;7-Bromoquinoline-2-carboxaldehyde
• CAS NO: 904369-20-6
• Molecular Formula: C₁₀H₆BrNO
• Molecular Weight: 236.06474
• Mol File: 904369-20-6.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 7-Bromo-quinoline-2-carbaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 7-Bromo-quinoline-2-carbaldehyde(904369-20-6)
• EPA Substance Registry System: 7-Bromo-quinoline-2-carbaldehyde(904369-20-6)

Safety Data

• Hazardous Substances Data: 904369-20-6(Hazardous Substances Data)

Usage

Uses

7-Bromoquinoline-2-carboxaldehyde is a reagent used in the synthesis of analogs which acts as an inhibitors of lymphocyte pore-forming protein perforin.

Upstream product

• 591-19-5 m-Bromoaniline 
• 4965-34-8 2-methyl-7-bromo-quinoline 
• 1267481-50-4 (7-bromoquinolin-2-yl)methanol 
• 1057217-63-6 7-bromoquinoline-2-carboxylic acid 

Downstream Products

• 1352204-62-6 tert-butyl 4-(2-((3-phenylpropanoyloxy)methyl)quinolin-7-yl)piperazine-1-carboxylate 

Relevant articles and documents

Quinoline-Derived Two-Photon-Sensitive Octupolar Probes

A systematic study on quinoline-derived light sensitive probes, having third-order rotational symmetry is presented. The electronically linked octupolar structures show considerably improved linear and nonlinear photophysical properties under one- and two-photon irradiation conditions compared to the corresponding monomers. Photolysis of the three acetate derivatives shows strong structure dependency: whereas irradiation of the 6- and 7-aminoquinoline derivatives resulted in fast intramolecular cyclization and only trace amounts of fragmentation products, the 8-aminoquinoline derivative afforded clean and selective photolysis, with a sequential release of their acetate groups (δu [730]=0.67 GM).

MULTIPHOTON ACTIVABLE QUINOLINE DERIVATIVES, THEIR PREPARATION AND THEIR USES

The present invention relates to multiphoton activable organic compounds responding to the following formula (I). The present invention also relates to a method of synthesizing the compounds of the invention, to an aqueous solution comprising at least one compound of the invention, and to their specific uses. The present invention also concerns a method of liberating organic ligands, said method involving the step of irradiating a compound according to the invention.

X-ray and gamma-photon activable organic compounds, their preparation and their uses

The present invention relates to a X-ray and gamma-photon activable organic compound responding to the following formula (I): The present invention also relates to methods of synthesizing a compound according to the invention, and to an aqueous or physiological solution comprising at least one compound of the invention. The present invention also concerns a method of liberating a biologically active compound, said method involving the step of irradiating a compound or an aqueous or physiological solution according to the invention. Finally, the present invention relates to a pharmaceutical composition comprising a compound, or an aqueous or physiological solution according to the invention.