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2-{[(E)-thiophen-2-ylmethylidene]amino}benzenethiol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

7525-70-4

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7525-70-4 Usage

Molecular structure

A benzene ring attached to a thiol group and an E-thiophen-2-ylmethylidene amino group.

Type of compound

Organic compound.

Usage in organic synthesis

It is commonly used in organic synthesis due to its ability to act as a ligand in coordination chemistry.

Pharmaceutical research

The compound has potential biological activity, making it useful in pharmaceutical research.

Strong odor

2-[(E)-thiophen-2-ylmethylidene]aminobenzenethiol is known for its strong odor.

Hazardous substance

It is considered a hazardous substance and should be handled with caution.

Potential applications

The chemical may have potential applications in various fields such as agriculture, medicine, and materials science.

Further research

More research is needed to fully understand the properties and potential uses of 2-[(E)-thiophen-2-ylmethylidene]aminobenzenethiol.

Check Digit Verification of cas no

The CAS Registry Mumber 7525-70-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,2 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7525-70:
(6*7)+(5*5)+(4*2)+(3*5)+(2*7)+(1*0)=104
104 % 10 = 4
So 7525-70-4 is a valid CAS Registry Number.

7525-70-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(thiophen-2-ylmethylideneamino)benzenethiol

1.2 Other means of identification

Product number -
Other names 2-thiophene carboxaldehyde benzothiazoline

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:7525-70-4 SDS

7525-70-4Downstream Products

7525-70-4Relevant academic research and scientific papers

Comparison of chelating ability of NO-, NS-, ONS-, and ONO-type Schiff base derivatives and their stability constants of Bis-complexes with copper(II)

Atabey, Hasan,Findik, Esra,Sari, Hayati,Ceylan, Mustafa

, p. 109 - 120 (2014/02/14)

The present study includes important findings relating to the number of donor atoms, species of ligands, and stabilities of complexes. Stabilities of complexes between Cu(II) ion and NO-, NS-, ONS-, and ONO-type Schiff bases were compared. Acid-base properties of the Schiff bases were explained at 25 ± 0.1 ° C and ionic strength (I) of 0.1 M supported by NaCl. The Hyperquad computer program was used for calculation of dissociation and stability constants. The overall stability constants of their Cu(II) complexes were calculated and the various formed complexes between the Schiff bases with Cu(II) ion formulated as CuL2, CuHL2, CuH2L 2, and CuH-1L2(Cu (OH) L2). The complexes of ONS- and ONO-type tridentate ligands were more stable than those of NO- and NS-type bidentate ligands. TUeBITAK.

Synthesis and spectral studies of methylsilicon(IV) chloride complexes with biologically active heterocyclic benzothiazolines

Singh, Kiran,Tandon, J.P.

, p. 283 - 285 (2007/10/02)

Some neutral adducts of methylsilicon(IV) chlorides with nitrogen donor ligands, Me2SiCl2(HBZt) and Me3SiCl(HBZt)(HBZt = benzothiazolines), have been synthesised and characterised on the basis of elemental analysis, molecular weight, IR and NMR (1H and 13

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