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Acridine, 4-methyl-9-(trimethylstannyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

602302-61-4

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602302-61-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 602302-61-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,2,3,0 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 602302-61:
(8*6)+(7*0)+(6*2)+(5*3)+(4*0)+(3*2)+(2*6)+(1*1)=94
94 % 10 = 4
So 602302-61-4 is a valid CAS Registry Number.

602302-61-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethyl-(4-methylacridin-9-yl)stannane

1.2 Other means of identification

Product number -
Other names 4-methyl-9-trimethylstannylacridine

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:602302-61-4 SDS

602302-61-4Downstream Products

602302-61-4Relevant academic research and scientific papers

Chiral 1,8-Diarylnaphthalenes, Methods of Making Them, and Their Use as Sensors

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Page/Page column 20-21, (2010/11/29)

One aspect of the invention relates to 1,8-diarylnaphthalene compounds. In certain embodiments, a compound of the invention is an N-oxide of a 1,8-diarylnaphthalene. In certain embodiments, the aryl group is an optionally substituted acridyl group. In certain embodiments, a compound of the invention is a single steroisomer. In certain embodiments, a compound of the invention is a single enantiomer. Another aspect of the present invention relates to a method of detecting the presence of an analyte in a sample by monitoring the fluorescence of a compound of the invention in a sample. In certain embodiments, the analyte is a metal ion. Another aspect of the present invention relates to a method of determining the enantiomeric purity of an analyte by monitoring the fluorescence of a compound of the invention in the presence of the analyte. In certain embodiments, the analyte is a compound that is capable of hydrogen bonding.

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