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2-[4-(tert-butyl)phenoxy]nicotinic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54659-69-7

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54659-69-7 Usage

Class

Carboxylic acids and derivatives

Functional Groups

Nicotinic acid moiety
tert-butyl group
Phenoxy group

Role of Nicotinic Acid Moiety

Involved in metabolic processes; precursor for coenzymes nicotinamide adenine dinucleotide and nicotinamide adenine dinucleotide phosphate

Potential Applications

Drug design and development
Organic synthesis

Properties

Requires further investigation through research and experimentation.

Check Digit Verification of cas no

The CAS Registry Mumber 54659-69-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,6,5 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 54659-69:
(7*5)+(6*4)+(5*6)+(4*5)+(3*9)+(2*6)+(1*9)=157
157 % 10 = 7
So 54659-69-7 is a valid CAS Registry Number.

54659-69-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-tert-butylphenoxy)pyridine-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names -

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:54659-69-7 SDS

54659-69-7Downstream Products

54659-69-7Relevant academic research and scientific papers

Effective and efficient sensitisation of terbium luminescence at 355 nm with cell permeable pyrazoyl-1-azaxanthone macrocyclic complexes

Montgomery, Craig P.,Parker, David,Lamarque, Laurent

, p. 3841 - 3843 (2007)

Emissive terbium complexes, suitable for protein conjugation, incorporating a pyrazoyl-1-aza-xanthone chromophore have been prepared; they exhibit cellular uptake and possess a much lower sensitivity to excited state quenching. The Royal Society of Chemis

PYRIDYL-AZA(THIO)XANTHONE SENSITIZER COMPRISING LANTHANIDE(III) ION COMPLEXING COMPOUNDS, THEIR LUMINESCENT LANTHANIDE (III) ION COMPLEXES AND USE THEREOF AS FLUORESCENT LABELS.

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Page/Page column 34, (2010/08/08)

Lanthanide (III) Ion completing compound comprising: (1) a sensitizer moiety of Formula (I) in which: a is an integer from 1 to 4; b is an integer equal to 1 or 2; c is an integer equal to 1 or 2; (R1)a, (R2)b, (R3)C are t

LANTHANIDE (III) ION COMPLEXING COMPOUNDS, LUMINESCENT LANTHANIDE (III) ION COMPLEXES AND USE THEREOF AS FLUORESCENT LABELS

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Page/Page column 10; 25, (2009/03/07)

Lanthanide (III) ion complexing compound comprising: (1) a sensitizer moiety of formula (I) in which: a is an integer from 1 to 4; b is an integer equal 1 or 2; c is an integer equal to 1 or 2; (R1)a, (R2)b, (R3)C are the

Emissive and cell-permeable 3-pyridyl- and 3-pyrazolyl-4-azaxanthone lanthanide complexes and their behaviour in cellulo

Montgomery, Craig P.,New, Elizabeth J.,Palsson, Lars O.,Parker, David,Batsanov, Andrei S.,Lamarque, Laurent

experimental part, p. 2186 - 2213 (2010/03/30)

A series of seven emissive europium(III) and terbium(III) complexes was prepared, incorporating a 3-pyridyl-4-azaxanthone or 3-pyrazolyl-4-azaxanthone sensitising moiety within a polydentate macrocyclic ligand. High overall emission quantum yields in aqueous media are attenuated in the presence of protein or certain oxy anions due to displacement of the N,N′-chelated sensitiser. Nevertheless, these complexes are taken into cells and tend to localise over the first few hours in mitochondria before being trafficked to endosomal compartments. Cell uptake studies, in the presence of competitive inhibitors or promoters of well-defined uptake pathways, reveal a common uptake mechanism involving macropinocytosis.

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