35426-11-0

Basic information

• Product Name: acridin-9-ylmethanol
• Synonyms: acridin-9-ylmethanol;9-Acridinemethanol
• CAS NO: 35426-11-0
• Molecular Formula: C₁₄H₁₁NO
• Molecular Weight: 209.25
• Mol File: 35426-11-0.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 434.3°Cat760mmHg
• Flash Point: 216.5°C
• Appearance: /
• Density: 1.27g/cm³
• Vapor Pressure: 2.59E-08mmHg at 25°C
• Refractive Index: 1.74
• Storage Temp.: 2-8°C
• PKA: 13.45±0.10(Predicted)
• CAS DataBase Reference: acridin-9-ylmethanol(CAS DataBase Reference)
• NIST Chemistry Reference: acridin-9-ylmethanol(35426-11-0)
• EPA Substance Registry System: acridin-9-ylmethanol(35426-11-0)

Safety Data

• Hazardous Substances Data: 35426-11-0(Hazardous Substances Data)

Usage

General Description

Acridin-9-ylmethanol is a chemical compound with the molecular formula C14H11NO. It is a derivative of acridine, a heterocyclic organic compound. Acridin-9-ylmethanol has been studied for its potential use in fluorescence labeling and as a precursor for the synthesis of various organic compounds. It has also been investigated for its role in the development of pharmaceuticals and as a component in the production of dyes and pigments. Additionally, acridin-9-ylmethanol has been the subject of research in the field of organic chemistry for its unique reactivity and potential applications.

InChI:InChI=1/C14H11NO/c16-9-12-10-5-1-3-7-13(10)15-14-8-4-2-6-11(12)14/h1-8,16H,9H2

Upstream product

• 1473417-56-9 Boc-Ala-OAcm 
• 1473417-55-8 Boc-Gly-OAcm 

Relevant articles and documents

Fluorescent photoremovable precursor (acridin-9-ylmethyl)ester: Synthesis, photophysical, photochemical and biological applications

A series of carboxylic acids including amino acids were protected as their corresponding fluorescent ester conjugates by coupling with an environment sensitive fluorophore 9-methylacridine. Photophysical properties of all the ester conjugates along with the protecting group have been investigated. Interestingly, the emission properties of the ester conjugates and 9-methylacridine were found to be highly sensitive to polarity, H-bonding and pH of the environment. Photolysis of all the ester conjugates was carried out using UV light above 360 nm and it was found that in every case the corresponding carboxylic acids were released in high chemical yield. Further, intercalation and the preferred binding mode of acridine-9-methanol and its ester conjugates with DNA were studied. In vitro biological studies revealed that acridine-9-methanol has good biocompatibility, cellular uptake property and cell imaging ability. The Royal Society of Chemistry and Owner Societies 2013.