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29644-79-9

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29644-79-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29644-79-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,6,4 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 29644-79:
(7*2)+(6*9)+(5*6)+(4*4)+(3*4)+(2*7)+(1*9)=149
149 % 10 = 9
So 29644-79-9 is a valid CAS Registry Number.

29644-79-9SDS

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 (6E)-6-[(2-nitroanilino)methylidene]cyclohexa-2,4-dien-1-one

1.2 Other means of identification

Product number -
Other names Salicylaldehyd-(2-nitro-phenylimin)

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:29644-79-9 SDS

29644-79-9Downstream Products

29644-79-9Relevant articles and documents

Highly selective probes of copper(II) complexes for sulfide detection and cytotoxicity assay

Chen, Yanmei,Shang, Xuefang,Zhao, Xing,Li, Jie,Yuan, Jianmei,Chen, Hongli,Zhang, Jinlian,Wang, Tianyun

, p. 308 - 321 (2018/02/06)

Two probes based on novel Copper(II) complexes were developed in order to obtain H2S molecular probes with higher selectivity. The molecular structures of the complexes were characterized by 1H NMR, HRMS, IR and elemental analysis. The interaction of the compounds with biologically important anions and amino acids was determined by UV-vis and Fluorescence titration experiments. Results indicated that the compounds showed the highest binding ability for HS? among studied anions (AcO?, H2PO4 ?, F?, Cl?, Br? and I?) and amino acids (GSH, HCys and Cys) accompanied by blue shift phenomenon in pure DMSO and aqueous solution. The possible mechanism of host–guest interaction may be that the Copper(II) ion of complex was captured by HS? and free ligand released which showed a remarkable changes in UV-vis absorption. In addition, cytotoxicity of the synthesized compounds was studied on MCF-7 cells. Results indicated that the synthesized compounds had low cytotoxicity over a concentration range of 0–150 μg?mL?1, which exhibited that the synthesized probes could be used to detect H2S in vivo. The probes based on novel copper(II) complexes were synthesized and obtained by the reaction of substituent salicylaldehyde with amine derivatives, and then reacted with Cu(CH3COO)2·H2O, respectively. Investigation on the interference from other species suggested that copper(II) complexes have high selectivity for HS? over other anions (AcO?, (Formula presented.), F?, Cl?, Br? and I?), followed by the release of the copper ion to give a remarkable increase in UV–VIS absorption in pure DMSO solution and aqueous solution.

Synthesis and physicochemical characterization of some Schiff base complexes of chromium(III)

Dubey,Dubey,Mishra

experimental part, p. 1208 - 1212 (2009/03/11)

Some chromium(III) complexes of the type, [Cr(L)2(H 2O)2]Cl (1-10) [where L = Schiff bases (sbH, derived from the condensation of 2-amino pyridine, 2-aminophenol, o-toluidine, p-toluidine, 3-nitroaniline and anthranilic acid with salicylaldehyde/vanillin) and substituted benzimidazole/ benzoxazole or mercaptobenzimidazole] have been prepared by the reaction of chromium(III) chloride with corresponding ligands followed by immediate addition of ethanolic solution of anhydrous sodium acetate in 1:2 molar ratio. The resulting products have been characterized by elemental analysis, spectral (IR, UV-visible and FAB-mass) as well as magnetic susceptibility measurements. Octahedral structure is proposed for the complexes.

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