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Benzene-1,4-dicarbaldehyde dithiosemicarbazone is a complex organic compound with the chemical formula C10H10N4S2. It is derived from benzene-1,4-dicarbaldehyde, which is a dicarboxaldehyde with two aldehyde groups attached to the 1 and 4 positions of a benzene ring. The compound is formed by the reaction of benzene-1,4-dicarbaldehyde with dithiosemicarbazone, a sulfur-containing derivative of semicarbazide. This results in a molecule with two semicarbazone moieties attached to the aldehyde groups, forming a dithio derivative. Benzene-1,4-dicarbaldehyde dithiosemicarbazone is known for its potential applications in analytical chemistry, particularly as a reagent for the detection and quantification of metal ions, due to its ability to form stable complexes with various metals.

3525-74-4

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3525-74-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3525-74-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,2 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3525-74:
(6*3)+(5*5)+(4*2)+(3*5)+(2*7)+(1*4)=84
84 % 10 = 4
So 3525-74-4 is a valid CAS Registry Number.

3525-74-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name [(E)-[4-[(Z)-(carbamothioylhydrazinylidene)methyl]phenyl]methylideneamino]thiourea

1.2 Other means of identification

Product number -
Other names 2-({4-[N-(carboxymethyl)carbamoyl]phenyl}carbonylamino)acetic acid

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:3525-74-4 SDS

3525-74-4Relevant academic research and scientific papers

Synthesis, physicochemical and optical properties of bis-thiosemicarbazone functionalized graphene oxide

Kumar, Santosh,Wani, Mohmmad Y.,Arranja, Claudia T.,Castro, Ricardo A.E.,Paix?o, José A.,Sobral, Abilio J.F.N.

, p. 183 - 188 (2018)

Fluorescent materials are important for low-cost opto-electronic and biomedical sensor devices. In this study we present the synthesis and characterization of graphene modified with bis-thiosemicarbazone (BTS). This new material was characterized using Fo

Synthesis and crystal structure of terephthalaldehyde-bis- (thiosemicarbazone)-bis-(dimethyl sulfoxide) solvate

Li, Peiyuan,Su, Wei,Liu, Lifeng,Chen, Rui,Huo, Lini

, p. 2319 - 2320 (2013)

A thiosemicarbazone single crystal synthesized with a formula as C 10H12N6S2 2C2H 6OS, was synthesized by 1,4-phthalaldehyde and 4- methylthiosemicarbazide. The crystal is triclinic, space group P-1 with unit cell parameters: a = 5.9519(5) A, b = 7.4721(7) A, c = 12.5450(13), α = 77.348(8)°, β = 78.672(8)°, γ = 79.193(7)°, V = 527.64(8) A3, Z = 1, Mr = 436.63, Dc = 1.374 g/cm3, μ = 0.471 mm-1, F(000) = 230, R = 0.0844, wR = 0.2607 for 1902 reflections with I > 2σ (I).

Terephthalaldehyde: An Effecient Key Precursor for Novel Synthesis of Some Interesting Bis-thiazoles and Bis-triazolopyrimidinones

Gomha, Sobhi M.,Farghaly, Thoraya A.,Abbas, Eman M. H.,Alqurashi, Nadia T.

, p. 750 - 755 (2018)

Novel bis-thiazoles were synthesized in high and efficient yields from the reaction of thiosemicarbazones with halogenated compounds. Also, new bis-triazolopyrimidines were prepared from the reaction of hydrazonoyl chlorides with bis-thione derivative. All prepared compounds were fully characterized by spectral methods. The synthesized bis-compounds will be attractive species for the medicinal researchers to investigate their biological activity.

Synthesis, characterization of thiosemicarb?zone metal complexes and their antioxidant activity in different in vitro model systems

Reddy, Desireddy Harikishore Kumar,Lee, Seung-Mok,Seshaiah, Kalluru,Babu, K. Ramesh

, p. 229 - 240 (2013)

The synthesis of bimetallic Cu(II), Co(II), Ni(II), Zn(II) and U(VI) complexes with general stoichiometry [H2L M(X2)(H 2O)2] (where H2L is the di-deprotanated ligand and X is chloride/sulphate) were o

Utilization of ultrasonic irradiation as green and effective one-pot protocol to prepare a novel series of bis-2-amino-1, 3, 4-oxa(thia)diazoles and bis-tetrazoles

Arafa, Wael Abdelgayed Ahmed,Abdel-Magied, Ahmed Fawzy

, p. 327 - 340 (2017/12/06)

In an effective and straightforward conversion, bis-semicarbazones and bis-thiosemicarbazones are transformed into a diversity of novel substituted bis-2-amino-1, 3, 4-oxadiazoles and bis-2-amino-1, 3, 4-thiadiazoles, respectively under ultrasonic irradiation. Bis-tetrazoles are obtained from the dialdehydes by sequential reaction with hydroxylamine hydrochloride, phosphorus pentoxide and sodium azide without isolation of the intermediates oximes and nitriles. All the reactions proceed cleanly and smoothly under mild conditions, with short reaction times and broad functional groups possibility. No side reactions were observed.

Synthesis, molecular docking, acetylcholinesterase and butyrylcholinesterase inhibitory potential of thiazole analogs as new inhibitors for Alzheimer disease

Rahim, Fazal,Javed, Muhammad Tariq,Ullah, Hayat,Wadood, Abdul,Taha, Muhammad,Ashraf, Muhammad,Qurat-Ul-Ain,Khan, Muhammad Anas,Khan, Fahad,Mirza, Salma,Khan, Khalid M.

, p. 106 - 116 (2015/09/02)

A series of thirty (30) thiazole analogs were prepared, characterized by 1H NMR, 13C NMR and EI-MS and evaluated for Acetylcholinesterase and butyrylcholinesterase inhibitory potential. All analogs exhibited varied butyrylcholinester

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