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951-00-8 Usage

Description

9,10-dimethyl-4a,10-dihydroacridine is a chemical compound with the molecular formula C15H15N. It is a polycyclic aromatic hydrocarbon derivative known for its unique chemical and physical properties, such as high stability and solubility in organic solvents. 9,10-dimethyl-4a,10-dihydroacridine is commonly used in the synthesis of various pharmaceuticals and dyes, and has been the subject of research in drug discovery and development due to its promising biological activities and potential therapeutic applications in the treatment of various diseases.

Uses

Used in Pharmaceutical Synthesis:
9,10-dimethyl-4a,10-dihydroacridine is used as a key intermediate in the synthesis of various pharmaceuticals for its potential therapeutic applications in the treatment of different diseases. Its unique chemical properties make it a valuable component in the development of new drugs.
Used in Dye Synthesis:
9,10-dimethyl-4a,10-dihydroacridine is used as a precursor in the synthesis of dyes due to its polycyclic aromatic structure, which contributes to the color and properties of the resulting dyes.
Used in Organic Synthesis:
9,10-dimethyl-4a,10-dihydroacridine is used as a versatile building block in organic synthesis, allowing for the creation of a wide range of chemical compounds with diverse applications.
Used in Medicinal Chemistry Research:
9,10-dimethyl-4a,10-dihydroacridine is used as a subject of research in medicinal chemistry, where its biological activities and potential therapeutic applications are explored for the development of new treatments and therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 951-00-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,5 and 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 951-00:
(5*9)+(4*5)+(3*1)+(2*0)+(1*0)=68
68 % 10 = 8
So 951-00-8 is a valid CAS Registry Number.

951-00-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 9,10-dimethylacridin-10-ium,iodide

1.2 Other means of identification

Product number -
Other names 9,10-Dimethyl-acridinium,Jodid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:951-00-8 SDS

951-00-8Relevant articles and documents

Acridine-based dyes as high-performance near-infrared Raman reporter molecules for cell imaging

Cao, Hui,Du, Jiasheng,He, Wanli,Li, Jinming,Li, Yuzhan,Wang, Dong,Zhou, Yang

, p. 3380 - 3385 (2022/02/09)

A surface-enhanced Raman scattering (SERS) nanoprobe has been proven to be a promising tool for near-infrared (NIR) biomedical imaging and diagnosis because of its high sensitivity and selectivity. However, the development of NIR SERS reporters has been a bottleneck impeding the preparation of ultrasensitive SERS probes. Herein, we report the design and synthesis of a series of SERS reporters in the NIR region based on 10-methylacridine (AD). The AD nanotags (gold nanostar-AD molecules-BSA, AuNS-AD-BSA) exhibit appreciable SERS signals and can be detected at as low as the sub-picomole level. The results of in vitro imaging experiments show that it can be used in live-cell delineation.

Synthesis and spectroscopic and DNA-binding properties of fluorogenic acridine-containing cyanine dyes

Mahmood, Tariq,Paul, Alexis,Ladame, Sylvain

scheme or table, p. 204 - 207 (2010/04/24)

(Chemical Equation Presented) The synthesis of a new subclass of mono- and polymethine cyanine dyes that incorporate an acridinium moiety and that absorb in the orange to near-infrared region of the spectrum is reported. The mono-, tri-, and pentamethine dyes in particular exhibit promising fluorogenic properties. Their ability to aggregate in solution and to interact with B-DNA is also discussed.

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