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2,6-bis(hydroxymethyl)-4-methylpyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

506423-84-3

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506423-84-3 Usage

Derived from

Pyridine

Contains

Two hydroxymethyl groups and a methyl group attached to the pyridine ring

Used in

Production of pharmaceuticals

Known for

Chelating metal ions

Potential use

Treatment of neurological disorders and as an antioxidant

Toxicity

Low

Commonly used in

Research and industrial applications

Check Digit Verification of cas no

The CAS Registry Mumber 506423-84-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,6,4,2 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 506423-84:
(8*5)+(7*0)+(6*6)+(5*4)+(4*2)+(3*3)+(2*8)+(1*4)=133
133 % 10 = 3
So 506423-84-3 is a valid CAS Registry Number.

506423-84-3Relevant academic research and scientific papers

Syntheses and anti-HIV and human cluster of differentiation 4 (CD4) down-modulating potencies of pyridine-fused cyclotriazadisulfonamide (CADA) compounds

Lumangtad, Liezel A.,Claeys, Elisa,Hamal, Sunil,Intasiri, Amarawan,Basrai, Courtney,Yen-Pon, Expedite,Beenfeldt, Davison,Vermeire, Kurt,Bell, Thomas W.

, (2020/11/20)

CADA compounds selectively down-modulate human cell-surface CD4 protein and are of interest as HIV entry inhibitors and as drugs for asthma, rheumatoid arthritis, diabetes and some cancers. Postulating that fusing a pyridine ring bearing hydrophobic subst

Concave pyridines with extended π-systems

Storm, Ole,Luening, Ulrich

, p. 3680 - 3685 (2007/10/03)

New 4-substituted concave pyridines 1b-d have been synthesised as precursors to allow extension of the pyridine π-system. With the Sonogashira coupling as the key synthetic step, the 4-iodo pyridine 1c was coupled with phenylacetylene (11) to give 1g in 77% yield. Because of its conjugated π system, the new concave pyridine 1g has UV absorption maxima at λmax1 = 286 nm and λmax2 = 303 nm with εmax1 = 43300 Lmol-1cm-1 and εmax2 = 39300 Lmol-1cm-1, respectively, allowing its potential application as a sensor. ( Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002).

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