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3-Pyridinol, 2-[[(2-hydroxyphenyl)methylene]amino]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38016-39-6

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38016-39-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38016-39-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,0,1 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 38016-39:
(7*3)+(6*8)+(5*0)+(4*1)+(3*6)+(2*3)+(1*9)=106
106 % 10 = 6
So 38016-39-6 is a valid CAS Registry Number.

38016-39-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-[[(3-hydroxypyridin-2-yl)amino]methylidene]cyclohexa-2,4-dien-1-one

1.2 Other means of identification

Product number -
Other names 2-[[(2-hydroxyphenyl)methylidene]amino]pyridin-3-ol

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:38016-39-6 SDS

38016-39-6Downstream Products

38016-39-6Relevant academic research and scientific papers

Synthesis, solvatochromaticity and bioactivities of some transition metal complexes with 2-(R-benzylideneamino)-pyridin-3-ol Schiff base derivatives

Ahmed,Kassem

, p. 359 - 366 (2010)

New four Schiff bases are prepared by condensation of 2-amino-pyridin-3-ol with 3, 4-dihydroxy-benzaldehyde (I), 2-hydroxybenzaldehyde (II), 5-bromo-2-hydroxybenzaldehyde (III), and 4-dimethylaminobenzaldehyde (IV). The structures of these compounds are characterized based on elemental analyses (C. H. N), IR and 1H NMR. Also, the electronic absorption spectra are recorded in organic solvents of different polarity. The solvents are selected to be covered a wide range of parameters (refractive index, dielectric constant and hydrogen bonding capacity). The UV-vis absorption spectra of Schiff base compounds are investigated in aqueous buffer solutions of varying pH and utilized for the determination of ionization constant, pKa and activation free energy, ΔG* of the ionization process. The biological activity against bacterial species and fungi as microorganisms representing different microbial categories such as (two Gram-negative bacteria, Eschericha coli and Agrobacterium sp.),three Gram-positive bacteria (Staphylococcus aureus, Bacillus subtlus and Bacillus megatherium), yeast (Candida albicans), and fungi (Aspergillus niger) were studied.

Desmotropy, polymorphism, and solid-state proton transfer: Four solid forms of an aromatic o-hydroxy schiff base

Rubcic, Mirta,Uzarevic, Krunoslav,Halasz, Ivan,Bregovic, Nikola,Malis, Momir,Dilovic, Ivica,Kokan, Zoran,Stein, Robin S.,Dinnebier, Robert E.,Tomisic, Vladislav

experimental part, p. 5620 - 5631 (2012/06/17)

The Schiff base derived from salicylaldehyde and 2-amino-3-hydroxypyridine affords a diversity of solid forms, two polymorphic pairs of the enol-imino (D1a and D1b) and keto-amino (D2a and D2b) desmotropes. The isolated phases, identified by IR spectrosco

H NMR, IR and UV/VIS spectroscopic studies of some Schiff bases derived from 2-aminobenzothiazole and 2-amino-3-hydroxypyridine

Issa, Raafat M.,Khedr, Abdalla M.,Rizk, Helen

body text, p. 875 - 884 (2009/12/04)

By condensing 2-aminobenzothiazole with 2-hydroxy-1-naphthaldehyde, 2-hydroxybenzaldehyde, 4-methoxybenzaldehyde, 4-hydroxybenzal-dehyde, benzaldehyde and 4-dimethylaminobenzaldehyde, and five Schiff bases Ia-Ie are prepared. Also, two Schiff bases IIa an

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