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94-90-6

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94-90-6 Usage

Chemical origin

Derived from salicylaldehyde and guanidine.

Structural feature

Contains a salicylideneamino group.

Potential medicinal applications

Investigated for its potential antiproliferative and antitumor properties.

Metal ion chelation

Ability to chelate metal ions.

Industrial applications

Potentially serves as a corrosion inhibitor.

Antimicrobial activity

Studied for its potential antimicrobial activities.

Antiviral activity

Studied for its potential antiviral activities.

Research and development

Diverse range of potential applications makes it an interesting and promising compound for further research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 94-90-6 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 9 and 4 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 94-90:
(4*9)+(3*4)+(2*9)+(1*0)=66
66 % 10 = 6
So 94-90-6 is a valid CAS Registry Number.

94-90-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Benzaldehyde, 2-hydroxy-, (aminoiminomethyl)hydrazone

1.2 Other means of identification

Product number -
Other names 2-Hydroxybenzaldehyde amidino hydrazone

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:94-90-6 SDS

94-90-6Downstream Products

94-90-6Relevant articles and documents

Biological promiscuity of a binuclear Cu(ii) complex of aminoguanidine Schiff base: DNA binding, anticancer activity and histidine sensing ability of the complex

Bauzá, Antonio,Chattopadhyay, Shyamal Kumar,Corbella, Montse,Das Saha, Krishna,Das, Chandrima,Frontera, Antonio,Mondal, Antu,Mondal, Sanchaita,Saha, Moumita

, p. 7319 - 7328 (2020)

A tridentate N,N,O-donor ligand, in the form of a Schiff base of aminoguanidine (LH) with salicylaldehyde, and its Cu(ii) complex, [Cu2(LH)2](ClO4)2, have been synthesized. The single crystal X-ray structure of the complex is reported. The complex shows strong DNA binding affinity, with a binding constant value comparable to that of classical intercalators like ethidium bromide. Against the human colon cancer cell line HCT116, the complex shows significant in vitro cytotoxicity with a LD50 value of 20 μM. It is shown that the cytotoxicity of the complex follows the apoptosis mechanism. The complex can also be used for selective spectrophotometric or fluorometric determination of histidine. The binuclear Cu(ii) complex shows strong intramolecular antiferromagnetic interaction between the Cu(ii) atoms mediated by two bridging phenoxide ligands, with 2J = -656 cm-1. DFT calculations are used to explain the magnetic interaction.

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