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3-ethyl-2-methylnaphtho[2,1-d][1,3]oxazol-3-ium iodide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54581-50-9

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54581-50-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54581-50-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,5,8 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 54581-50:
(7*5)+(6*4)+(5*5)+(4*8)+(3*1)+(2*5)+(1*0)=129
129 % 10 = 9
So 54581-50-9 is a valid CAS Registry Number.

54581-50-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-ethyl-2-methylbenzo[g][1,3]benzoxazol-3-ium,iodide

1.2 Other means of identification

Product number -
Other names Naphth(2,1-d)oxazolium,3-ethyl-2-methyl-,iodide

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:54581-50-9 SDS

54581-50-9Downstream Products

54581-50-9Relevant academic research and scientific papers

A New Method for the Synthesis of Heptamethine Cyanine Dyes: Synthesis of New Near-Infrared Fluorescent Labels

Narayanan, Narasimhachari,Patonay, Gabor

, p. 2391 - 2395 (1995)

A new uncatalyzed synthesis of heptamethine cyanine dyes is described.The reaction involves heating a mixture of N-alkyl-substituted quaternary salts derived from 2,3,3-trimethylindole or 2,3,3-trimethylbenzindole and 2-chloro-1-formyl-3-(hydroxymethylene)cyclohex-1-ene to reflux in a mixture of 1-butanol and benzene (7:3) as solvent.No catalyst is used, and water is removed as an azeotrope.The resulting chloro compounds possess strong absorption and fluorescence properties in the near-infrared region and are converted to dyes bearing reactive functionalities such as hydroxy and isothiocyanate groups useful as fluorescent tags for nucleic acids and proteins.Several symmetric and nonsymmetric dyes have been synthesized in high yields.

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