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Benzenamine, 2,2'-[1,3-propanediylbis(thio)]bis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60435-49-6

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60435-49-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60435-49-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,4,3 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 60435-49:
(7*6)+(6*0)+(5*4)+(4*3)+(3*5)+(2*4)+(1*9)=106
106 % 10 = 6
So 60435-49-6 is a valid CAS Registry Number.

60435-49-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[3-(2-aminophenyl)sulfanylpropylsulfanyl]aniline

1.2 Other means of identification

Product number -
Other names S,S'-di(2-aminophenyl)-1,3-dithiopropane

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:60435-49-6 SDS

60435-49-6Relevant academic research and scientific papers

Synthesis and characterization of some transition metal complexes with bis(o-aminophenyl)disulfide alkane ligands

Salih,Saeed

, p. 6821 - 6826 (2021/11/01)

A series of new complexes of the type [M(L)Cl2] and [M(L)]Cl2 where M= Co(II),Ni(II) and Cu(II), L=L1 or L2 {L1=1,2- Bis(o-aminophenyl)disulfide propane,L2=1,2-Bis(o- aminophenyl) disulfide butane, have been prepared in 1:1 (L:M) and characterized by mola

Piperazine-mediated tandem synthesis of bis(thieno[2,3-b]pyridines): Versatile precursors for related fused [1,2,4]triazolo[4,3-a]pyrimidines

Sanad, Sherif M. H.,Mekky, Ahmed E. M.

, p. 3142 - 3152 (2020/06/09)

In this study, we discuss the utility of bis(cyanoacetamides) as versatile precursors to the piperazine-mediated synthesis of a wide spectrum of bis(thieno[2,3-b]pyridine) derivatives, linked to aliphatic spacers via thioethers. The proposed tandem protoc

Bis(2-cyanoacetamides): Versatile precursors for bis(dihydropyridine-3,5-dicarbonitriles)

Sanad, Sherif M.H.,Elwahy, Ahmed H.M.,Abdelhamid, Ismail A.

, p. 39 - 49 (2018/10/26)

Bis(6-amino-1,2-dihydropyridine-3,5-dicarbonitriles) containing thioether linkages are prepared via the condensation of bis(cyanoacetamides) with α-substituted cinnamonitriles in the presence of piperidine. The target compounds can also be obtained via a three-component reaction of bis(cyanoacetamides) with two equivalents of both aldehydes and malononitrile in ethanol containing piperidine as a base.

Zinc oxide catalyzed solvent-free mechanochemical route for C-S bond construction: A sustainable process

Md. Khaja Mohinuddin,Gangi Reddy

, p. 1207 - 1214 (2017/12/07)

A zinc oxide catalyzed solvent-free mechanochemical process has been developed for the rapid construction of C-S bonds by using a nucleophilic substitution reaction (SN2 mechanism) that involves a variety of thiols and phenacyl/ benzyl/alkyl bromides. Notable advantages of this method in-clude its broad substrate scope, clean reaction profile, safety, scalability, high product yields at ambient conditions, and the recyclability of the catalyst. Furthermore, the prepared compounds are valuable building blocks for the synthesis of various biologically active molecules.

Synthesis and evaluation of bifunctional chelating agents derived from bis(2-aminophenylthio)alkane for radioimaging with 99mTc

Chhikara, Bhupender S.,Kumar, Nitin,Tandon, Vibha,Mishra, Anil K.

, p. 4713 - 4720 (2007/10/03)

Novel bifunctional chelating agents bearing an aromatic rigid backbone have been synthesized and characterized on the basis of spectroscopic techniques. These macrocyclic multidentate chelating agents were conjugated with monoclonal antibody which forms stable complexes with 99mTc with high radiochemical purity.

KF-alumina immobilized in ionic liquids: A novel heterogeneous base for heterocyclization of alkylsulfanylphenylamines into 1,4-benzothiazine

Chhikara, Bhupender S.,Mishra, Anil K.,Tandon, Vibha

, p. 1057 - 1065 (2007/10/03)

A rapid and convenient synthetic methodology for the cyclocondensative transformation of various alkylsulfanylphenylamines with bromoacetyl bromide by supporting on KF-alumina in ionic liquids [bmim] [Br] and [bmim][BF 4] has been developed to obtain 3-oxo-1,4-benzothiazine in good yields. The product is easily obtained by extraction with ethyl acetate and concentrating under vacuum. Easy recovery of ionic liquid and use in consecutive reactions is also reported.

Synthesis of new calix(aza) and calix(aza-thia) crowns

Kumar,Sharma nee Bhalla,Sharma

, p. 492 - 493 (2007/10/03)

The synthesis of new calix(aza), calix(aza-thia) crowns and bisbromoacetamides is reported in good yields.

Synthesis and structure of binuclear thioazobenzene pallada-cycles and their reaction with m-chloroperbenzoic acid: formation and structure of dinuclear azophenolates

Chattopadhyay, Surajit,Sinha, Chittaranjan,Choudhyry, Suranjan Bhanja,Chakravorty, Animesh

, p. 111 - 123 (2007/10/02)

The cyclopalladation of 1,3-bis(2-thioazobenzene)propane (L1H2) and its methyl substituted derivative L2H2 affords complexes of the type LPd2Cl2 (where L represents L1 or L2) which have been characterised by spe

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