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Benzenesulfonamide, N-(4,6-dimethyl-2-pyrimidinyl)-4-[[(2-hydroxyphenyl)methylene]amino]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16182-36-8

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16182-36-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16182-36-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,1,8 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 16182-36:
(7*1)+(6*6)+(5*1)+(4*8)+(3*2)+(2*3)+(1*6)=98
98 % 10 = 8
So 16182-36-8 is a valid CAS Registry Number.

16182-36-8SDS

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 N-(4,6-dimethyl-pyrimidin-2-yl)-4-(2-hydroxy-benzylideneamino)-benzenesulfonamide

1.2 Other means of identification

Product number -
Other names N-Salicyliden-sulfanilsaeure-(4,6-dimethyl-pyrimidin-2-ylamid)

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:16182-36-8 SDS

16182-36-8Downstream Products

16182-36-8Relevant academic research and scientific papers

Selective coordination ability of sulfamethazine Schiff-base ligand towards copper(II): Molecular structures, spectral and SAR study

Mansour, Ahmed M.

, p. 257 - 266 (2014)

In the present work, a combined experimental and theoretical study of the N-(4,6-Dimethyl-pyrimidin-2-yl)-4-[(2-hydroxy-benzylidene)amino] benzenesulfonamide ligand (H2L) and its mononuclear and magnetically diluted binuclear CuII complexes has been performed using IR, TG/DTA, magnetic, EPR, and conductivity measurements. Calculated g-tensor values showed best agreement with experimental values from EPR when carried out using the MPW1PW91 functional. Coordination of H2L to a CuII center, regardless of the binding site and Cu:L stoichiometry, leads to a significant decrease in the antibacterial activity compared to the free ligand as well as reference drugs in the case of Staphylococcus aureus. Structural-activity relationship suggests that ELUMO, ΔE, dipole moment, polarizability and electrophilicity index were the most significant descriptors for the correlation with the antibacterial activity.

Hydrogen-bond effect, spectroscopic and molecular structure investigation of sulfamethazine Schiff-base: Experimental and quantum chemical calculations

Mansour, Ahmed M.,Abdel Ghani, Nour T.

, p. 226 - 237 (2013)

Comprehensive theoretical and experimental structural studies on N-(4,6-dimethyl-pyrimidin-2-yl)-4-[(2-hydroxy-benzylidene)-amino] benzenesulfonamide (SMS) have been carried out by elemental analysis, FT IR, 1H NMR, UV-Vis. and MS. Optimized mo

Schiff bases derived from 4-amino-n-substituted benzenesulfonamide: Synthesis, spectral characterisation and mic evaluation

Nisha, Chinnadhurai,Sabarika, Balachandran,Subbalakshmi, Ramanathan,Valarmathy, Govindaraj

, p. 435 - 448 (2022/01/03)

The present study is aimed to synthesise Schiff bases from sulfathiazole/ sulfamethoxazole/ sulfadimidine with 2-hydroxybenzaldehyde. The synthesized Schiff bases were characterized by analytical data, IR, 1H-NMR, 13C-NMR, UV-Vis spe

Synthesis, molecular modeling, TD-DFT, antimicrobial, and in vitro therapeutic activity of new spherical nano-sized sulfonamide imine ligands and their zinc (II) and copper (II) complexes

El-Dissouky, Ali,Abu-Elsoud, Eslam S.,Abdel Razik, Afaf,Awad, Mohamed K.,Hassan, Hammed H.A.M.,Elhusseiny, Amel F.

, (2020/08/19)

A series of nanometer-sized spherical sulfonamide imine ligands HL1-HL5 and their copper and zinc complexes were synthesized and fully characterized based on elemental analyses, spectroscopic (UV/vis, FT-IR, NMR, EPR, SEM) studies, m

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