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Propanedinitrile, 2(3H)-benzothiazolylidene- (9CI), also known as 2-benzothiazolylidenepropanedinitrile or BTDN, is a chemical compound with the molecular formula C10H6N4S. It is a yellow crystalline solid that is soluble in organic solvents such as ethanol, acetone, and dimethyl sulfoxide. BTDN is a derivative of benzothiazole, a heterocyclic compound with a benzene ring fused to a thiazole ring. Propanedinitrile, 2(3H)-benzothiazolylidene- (9CI) has been studied for its potential applications in various fields, including pharmaceuticals, agrochemicals, and materials science. It is known for its ability to form complexes with metal ions, which can be useful in the development of new drugs or as analytical reagents. Additionally, BTDN has been investigated for its potential as a precursor in the synthesis of other benzothiazole-based compounds with diverse applications.

4464-52-2

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4464-52-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4464-52-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,6 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4464-52:
(6*4)+(5*4)+(4*6)+(3*4)+(2*5)+(1*2)=92
92 % 10 = 2
So 4464-52-2 is a valid CAS Registry Number.

4464-52-2SDS

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 (2,3-dihydrobenzothiazol-2-ylidenyl)malonodinitrile

1.2 Other means of identification

Product number -
Other names (3-hydrobenzothiazol-2-ylidenyl)malononitrile

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:4464-52-2 SDS

4464-52-2Relevant academic research and scientific papers

Domino Synthesis of 2-Substituted Benzothiazoles by Base-Promoted Intramolecular C-S Bond Formation

Kumar, Yogendra,Ila, Hiriyakkanavar

supporting information, p. 7863 - 7867 (2019/10/11)

A new, transition-metal-free, domino synthesis of 2-substituted benzothiazoles has been developed, involving base-promoted one-pot addition of active methylene compounds to o-iodoarylisothioacyanates and subsequent intramolecular C-S bond formation of the

2-[1H-Benzimidazol-2(3H)-ylidene]-2-(pyrimidin-2-yl)acetamides and 2-[benzothiazol-2(3H)-ylidene]-2-(pyrimidin-2-yl)acetamides as kinase inhibitors

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Page/Page column 17, (2010/04/25)

2-[1H-benzimidazol-2(3H)-ylidene]-2-(pyrimidin-2-yl)acetamides and 2-[benzothiazol-2(3H)-ylidene]-2-(pyrimidin-2-yl)acetamides and their salts are kinase inhibitors, useful in the treatment of cancer.

Synthesis of 4-amino-3-cyano-2-methylsulfanyl-1 H-[1,5]benzodiazepine, benzo[1,3]azole, and pyrazolobenzo[1,3]azole derivatives via a new utility of bis(methylsulfanyl)methylene derivatives

El-Rady, Eman A.,Khalil, Mohamed A.,Abd El Latif, Fawi M.

, p. 407 - 412 (2007/10/03)

Novel polysubstituted 1,5-benzodiazepine 5, 2,2-bis(methylthio)benzoxazoles 8a-d, 2,2-bis-(acetyl)benzoxazole 8e, 2-(3-methyl-1-phenylpyrazolo4-yl) benzoazole derivatives 16a-c, as well as the previously reported 2-di[cyano(acetyl)-methylene]benzothiazole

Chemical Interactions between 2-Mercaptobenzazoles and ?-Acceptors

Hassan, A. A.,Mohamed, N. K.,El-Tamany, E. H.,Ali, B. A.,Mourad, A. E.

, p. 653 - 662 (2007/10/02)

2-Mercaptobenzazoles (1a-c) interact with several ?-acceptors such as tetracyanoethylene (TCNE), 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ), 2,3,5,6-tetrachloro-1,4-benzoquinone (CHL), dicyanomethyleneindane-1,3-dione (CNIND), 2,3-dicyano-1,4-naphthoquinone (DCNQ), 9-dicyanomethylene-2,4,7-trinitrofluorene (DTF), and 2,3-dichloro-1,4-naphthoquinone (DCHNQ) via the formation of charge-transfer (CT) complexes to yield various heterocyclic compounds. - Keywords: 2-Mercaptobenzazoles; Molecular interactions; ?-Acceptors

SYNTHESIS OF SOME NEW FUSED HETEROCYCLES CONTAINING A BRIDGEHEAD NITROGEN ATOM UNDER PTC CONDITIONS. A NEW APPLICATION OF CYANOKETENE S,S-ACETALS

El-Shafei, Ahmed Kamal,Soliman, Ahmed Mohamed,Sultan, Adel Abdel-Rahim,El-Saghier, Ahmed Mohamed Mohamed

, p. 115 - 118 (2007/10/02)

A novel synthesis of some fused heterocyclic compounds containing a bridgehead nitrogen atom was achieved using PTC conditions.Suitable ketene S,S-acetals were thus prepared and allowed to react with some o-substituted anilines to give (2,3-dihydrobenzothiazol-2-ylidenyl)malonodinitrile, 2a, ethyl (2,3-dihydrobenzothiazol-2-ylidenyl)cyanoacetate, 2b, (2,3-dihydrobenzoxazol-2-ylidenyl)malonodinitrile, 2c, ethyl (2,3-dihydrobenzoxazol-2-ylidenyl)cyanoacetate, 2d, (2,3-dihydrobenzimidazol-2-ylidenyl)malonodinitrile, 2e, and ethyl (2,3-dihydrobenzimidazol-2-ylidenyl)cyanoacetate, 2f.These afforded the desired products on reaction with a variety of halo compounds.

Synthesis, Reactions, and Tautomerism of Ketene N,S-Acetals with Benzothiazoline Ring

Huang, Zhi-Tang,Shi, Xian

, p. 541 - 547 (2007/10/02)

Ketene dithioacetals 2 react with 2-aminothiophenol to afford the corresponding substituted 2(3H)-methylenebenzothiazoles 3.Some compounds 3 react with α,β-unsaturated esters to give 1H-pyridobenzothiazole derivatives 4 and 5 by an electrophilic addition and cyclocondensation sequence.

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