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Phenyl[5-(dimethylamino)-1-naphtylsulfonyl] ether is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55837-12-2

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55837-12-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55837-12-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,8,3 and 7 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 55837-12:
(7*5)+(6*5)+(5*8)+(4*3)+(3*7)+(2*1)+(1*2)=142
142 % 10 = 2
So 55837-12-2 is a valid CAS Registry Number.

55837-12-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-dimethylamino-naphthalene-1-sulfonic acid phenyl ester

1.2 Other means of identification

Product number -
Other names dansyl phenolate

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:55837-12-2 SDS

55837-12-2Downstream Products

55837-12-2Relevant academic research and scientific papers

Dansylated resorcinarenes

Kodiah Beyeh, Ngong,Aumanen, Jukka,Ahman, Antti,Luostarinen, Minna,Mansikkamaeki, Heidi,Nissinen, Maija,Korppi-Tommola, Jouko,Rissanen, Kari

, p. 370 - 376 (2007)

The synthesis, X-ray crystal structures and spectroscopic characterization (UV-Vis absorption and fluorescence emission) of regioselective tetradansylated resorcinarene 2 and octadansylated resorcinarene 3 are described. In solution, the resorcinarene bac

Profiling sulfonate ester stability: Identification of complementary protecting groups for sulfonates

Miller, Stephen C.

supporting information; experimental part, p. 4632 - 4635 (2010/09/17)

(Figure presented) Sulfonation is prized for its ability to impart water-solubility to hydrophobic molecules such as dyes. This modification is usually performed as a final step, since sulfonated molecules are poorly soluble in most organic solvents, which complicates their synthesis and purification. This work compares the intrinsic lability of different sulfonate esters, identifying new sulfonate protecting groups and mild, selective cleavage conditions.

Novel dansyl-appended calix[4]arene frameworks: Fluorescence properties and mercury sensing

Pandey, Shubha,Azam, Amir,Pandey, Siddharth,Chawla

scheme or table, p. 269 - 279 (2009/03/12)

Covalently-attached fluorophores may impart enhanced chemosensing capabilities to calixarene frameworks. Synthesis and characterization of six novel dansyl-appended calix[4]arenes, namely, H/Dan4, NO 2/Dan4, H/(OH)2/

Exchanged Fluorescence Detection of Dansyl Derivatives of Phenolic Compounds Using a Postcolumn Photochemical Reactor and Application to Chlorophenols in River Water

de Ruiter, Cornelis,Bohle, Jan F.,de Jong, Gerhardus J.,Brinkman, Udo A. Th.,Frei, Roland W.

, p. 666 - 670 (2007/10/02)

Photochemical decomposition by ultraviolet (UV) irradiatin of dansyl derivatives of phenolic compounds in methanol-water mixtures leads to the formation of highly fluorescent dansyl-OH and dansyl-OCH3.With substituted phenols as model compounds, it is dem

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