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1H-Benzotriazole-1-acetonitrile is an organic compound that features a benzotriazole core fused with an acetonitrile group. It is known for its versatile reactivity and stability, making it a valuable intermediate in the synthesis of various organic and medicinal compounds.

111198-08-4

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111198-08-4 Usage

Uses

Used in Organic Synthesis:
1H-Benzotriazole-1-acetonitrile is used as a reactant for hydrothermal reactions, which are important for the synthesis of various organic compounds under high temperature and pressure conditions.
Used in Green Luminance Dyes:
1H-Benzotriazole-1-acetonitrile is used as a reactant for the preparation of aminonaphthylacrylonitrile derivatives, which serve as green luminance dyes. These dyes are environmentally friendly and have potential applications in various industries.
Used in Antibacterial Agents:
1H-Benzotriazole-1-acetonitrile is used as a reactant for the preparation of (aminomethyl)(cyanovinylphenyl)oxazolidinones with heterocyclic pendants. These compounds exhibit antibacterial properties and can be used in the development of new antibiotics.
Used in Cyclization Reactions:
1H-Benzotriazole-1-acetonitrile is used in cyclization reactions with sodium azide, which can lead to the formation of various heterocyclic compounds with potential applications in pharmaceuticals and materials science.
Used in Antitumor Agents:
1H-Benzotriazole-1-acetonitrile is used as a reactant for the preparation of substituted triazoles, which have been identified as potential antitumor agents. The synthesis involves a rearrangement reaction followed by a cycloaddition of the corresponding (cyanomethyl)benzotriazole.
Used in Antifungal and Antiproliferative Agents:
1H-Benzotriazole-1-acetonitrile is a useful reactant for the preparation of tubulin-modulating pyrazinone derivatives, which exhibit antifungal and antiproliferative properties. These compounds have potential applications in the development of new antifungal and anticancer drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 111198-08-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,1,9 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 111198-08:
(8*1)+(7*1)+(6*1)+(5*1)+(4*9)+(3*8)+(2*0)+(1*8)=94
94 % 10 = 4
So 111198-08-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H6N4/c9-5-6-12-8-4-2-1-3-7(8)10-11-12/h1-4H,6H2

111198-08-4 Well-known Company Product Price

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  • Aldrich

  • (467529)  1H-Benzotriazole-1-acetonitrile  95%

  • 111198-08-4

  • 467529-1G

  • 1,297.53CNY

  • Detail
  • Aldrich

  • (467529)  1H-Benzotriazole-1-acetonitrile  95%

  • 111198-08-4

  • 467529-5G

  • 5,280.21CNY

  • Detail

111198-08-4SDS

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 1H-Benzotriazole-1-Acetonitrile

1.2 Other means of identification

Product number -
Other names Benzotriazol-1-ylacetonitrile

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:111198-08-4 SDS

111198-08-4Relevant academic research and scientific papers

Hydrothermal synthesis of two Zinc coordination Polymers with 1-(1H-Tetrazol-5-ylmethyl)-1H-benzotriazole Ligands

Sun, Su-Wen,Jin, Lei,Shi, Ping-Ping,Liu, Ming-Liang,Kong, Li-Hui,Ye, Qiong

, p. 2317 - 2323 (2013)

The direct reaction of ZnBr2 with H-1-mbtz [1-mbtz = 1- (1H-tetrazol-5-ylmethyl)-1H-benzotriazole] gives the two-dimensional complex [Zn(Br)(1-mbtz)] (1), whereas the reaction of benzotriazol-1- yl-acetonitrile with NaN3 in the presence of water and a Lewis acid (ZnBr2) affords the 2D coordination polymer [Zn2(OH)(1-mbtz)3H2O] (2). The central zinc atom in 1 is bonded to one terminal bromine atom and three different nitrogen atoms from two tetrazole ligands and one BTA group (BTA = benzotriazole), and each 1-mbtz ligand is coordi- nated to three zinc atoms forming a 2D framework. The coordination polyhedron around the metal atom in 2 is a slightly distorted trigonal bipyramid made up by one zinc atom, four nitrogen atoms as well as one oxygen atom, two of the 1-mbtz ligands coordinated to three zinc atoms and the third 1-mbtz ligand acts in a bidentate fashion, which leads to the formation of a complicated 2D network. The syntheses and solid-state structures of the two coordination polymers are reported.

Synthesis and anticancer activity of benzotriazole derivatives

Li, Qiujing,Li, Zhulai,Liu, Guijun,Wang, Ningning,Yin, Huiyong

, (2019)

A series of benzotriazole (BTA) derivatives were synthesized as tyrosine protein kinase inhibitors using fragment-based design strategy. All desired compounds were synthesized with the reaction of benzotriazole, chloroacetonitrile and aromatic aldehyde using Ultrasonic-Microwave method and characterized by IR, 1H and 13C-NMR, mass spectrometry (MS) and elemental analysis. The anticancer activity of these compounds was evaluated by CCK-8 method against carcinoma VX2, lung cancer A549, stomach cancer cell lines MKN45 and MGC in vitro. The results showed that all compounds showed good antiproliferative activity. In particular, compound 2.1 showed the most prominent inhibition of VX2 cell lines with IC50 of 3.80 ± 0.75 μM. Compound 2.2 exhibited highly potent anticancer activity of stomach MGC cell lines with IC50 of 3.72 ± 0.11 μM. A549 and MKN45 cell lines were sensitive to compound 2.5 with IC50 of 5.47 ± 1.11 and 3.04 ± 0.02 μM, respectively.

Synthesis and antimicrobial of some new substituted tetrazolomethylbenzo[d] -[1,2,3]triazole derivatives using 1H-benzo[d][1,2,3]triazole as starting material

Ali, Omar M.,Amr, Abd El-Galil E.,Mostafa, Elsayed E.

, p. 1545 - 1556 (2014)

A series of tetrazolomethylbenzo[d][1,2,3]triazole derivatives (2-14) have been synthesized and evaluated as antimicrobial agents from 1H-benzo[d][1,2,3] triazole (1) as starting material. The reaction of benzotriazole 1 with chloroacetonitrile afforded 2-(1H-benzo[d][1,2,3]-triazol-1-yl)acetonitrile 2, which was reacted with sodium azide to give tetrazole derivative 3. Esterification of benzotriazole 1 with ethyl bromoacetate in the presence of anhydrous potassium carbonate afforded ester 4, which was treated with hydrazine hydrate to afford the corresponding hydrazide 5. Reaction of 3 with 2,3,4,6-tetra-O-acetyl-α-d-glucopyranosyl bromide afforded the nitro-glycoside derivative 6, which was deacetylated using methanolic ammonia to deprotected nitroglycoside 7. The hydrazide 5 was reacted with 4,5,6,7-tetrachlorophthalic anhydride or 1,2,4,5-benzenetetracarboxylic dianhydride in refluxing glacial acetic acid to give the corresponding imides 8 and 9, respectively. Also, the hydrazide 5 was reacted with carbon disulphide in ethanol to give potassium salt 10, which was reacted with hydrazine hydrate to afford aminotriazole derivative 11. The latter compound was reacted with carbon disulphide to afford thiadiazole derivative 12, which was treated with 2,3,4,6-tetra-O-acetyl-α-d-glucopyranosyl bromide to give the thioglycoside derivative 13. Deacetylation of the thioglycoside 13 using methanolic ammonia solution at room temperature afforded the deprotected thioglycoside 14. The antimicrobial screening of some synthesized compounds showed that many of these compounds have good antimicrobial activities comparable to streptomycin and fusidic acid as reference drugs.

Synthesis and characterization of benzotriazolyl acrylonitrile analogs-based donor-acceptor molecules: Optical properties, in vitro cytotoxicity, and cellular imaging

Hernández-Fernández, Eugenio,Ortega-Villarreal, Ana Sofia,García-López, Ma. Concepción,Chan-Navarro, Rodrigo,Garrard, Samuel,Valdivia-Berroeta, Gabriel A.,Smith, Stacey J.,Christensen, Kenneth A.,Michaelis, David J.

, (2021)

A series of eight new (E)-benzotriazolyl acrylonitrile derivatives were synthesized under reflux conditions via Knoevenagel condensation between acetonitrile analogs and a short series of aromatic aldehydes. X-ray diffraction analysis for one of the compounds was performed to determine the (E)-geometry of its double bond. The photoluminescent properties of all compounds in solution were also evaluated. These compounds exhibit strong blue, green and yellow emission under ultraviolet light excitation with fluorescence quantum yield in the 0.08–0.58% range. To determine the suitability of these compounds for use in cell-based analysis, cytotoxicity assays were performed on a representative molecule using a common mammalian cell line (HEK 293T cells) at different concentrations. The results showed limited toxicity (72 ± 16% viability) at the highest concentration tested (50 μM). Finally, confocal microscopy demonstrated that our compound was internalized into cells and localized to endosomes and/or lysosomes in a similar fashion to Dextran–Cascade Blue (DCB).

Benzotriazole-Assisted Preparations of 2-(Substituted amino)pyridines and Pyrid-2-ones

Katritzky, Alan R.,Belyakov, Sergei A.,Sorochinsky, Alexander E.,Henderson, Scott A.,Chen, Jie

, p. 6210 - 6214 (1997)

Base-promoted reactions of benzotriazolyl-containing acetic acid derivatives, 2-(benzotriazol-1-yl)acetonitrile (7a), 2-(benzotriazol-1-yl)acetamide (7b), and (±)-2-(benzotriazol-1-yl)propionamide (7c), with α,β-unsaturated ketones 8 give efficient and regioselective access to previously difficult to attain 3-unsubstituted pyridine derivatives: the 2-(substituted amino)pyridines 14a-k and the 4,6-substituted pyrid-2-ones 15a-h. The pyridine rings result from tandem [3 + 3] annulations involving a Michael addition followed by cyclization.

Synthesis, crystal structure and photo- and electro-luminescence of the coumarin derivatives with benzotriazole moiety

Yu, Tianzhi,Zhang, Peng,Zhao, Yuling,Zhang, Hui,Meng, Jing,Fan, Duowang,Chen, Lili,Qiu, Yongqing

, p. 41 - 49 (2010)

Two new coumarin derivatives containing an electron-transporting moiety (benzotriazole), 7-N,N-diethylamino-3-(benzotriazol-1-yl)coumarin (DABTC-1) and 7-N,N-diethylamino-3-(benzotriazol-2-yl)coumarin (DABTC-2), were synthesized and characterized by element analysis, 1H NMR, FT-IR and UV-vis absorption spectra. Their structures were determined by X-ray crystallography single crystal analysis. The photoluminescent behaviors of the compounds in both solution and solid states were observed, they exhibit strong blue and blue-green emissions under ultraviolet light excitation, respectively. The energy levels of the HOMO and LUMO of the compounds have been calculated with density functional theory (DFT) and time-dependent density functional theory (TD-DFT) at B3LYP/6-31G(d) level. The electroluminescent devices with the compounds as the emitters were fabricated.

Synthesis and antiproliferative activity of 3-aryl-2-[1H(2H)-benzotriazol- 1(2)-yl]acrylonitriles variously substituted: Part 4

Carta, Antonio,Palomba, Michele,Boatto, Gianpiero,Busonera, Bernardetta,Murreddu, Marta,Loddo, Roberta

, p. 637 - 644 (2004)

A new series of variously substituted 3-aryl-2-[1H(2H)-benzotriazol-1(2)- yl]acrylonitriles was synthesized and tested for antiproliferative and antitubercular activity as part of our continuing research program in the antimicrobial and antitumor fields. The most cytotoxic derivatives (5a,g,i,j,l and 7b) (CC50 3.0 μM against MT-4 cells) were evaluated against a panel of human cell lines derived from hematological and solid tumors, using 6-mercaptopurine (6-MP) and etoposide as reference drugs. In particular, E-2-(5,6-dimethyl-1H-benzotriazol-1-yl)-3-(3-nitrophenyl)acrylonitrile (5g) resulted more potent than 6-MP on all cell lines, even if 2-14-fold less potent than etoposide. In the antitubercular screening, the derivatives 5i,j and 7e showed moderate activity against some resistant strains of Mycobacterium tested.

Perfluorobutyl iodide-assisted direct cyanomethylation of azoles and phenols with acetonitrile

Zhang, Juan,Wu, Wei,Ji, Xinfei,Cao, Song

, p. 20562 - 20565 (2015/03/30)

A perfluorobutyl iodide-assisted transition-metal-free cyanomethylation of azoles and phenols with acetonitrile in the presence of NaH has been developed. The reaction proceeded smoothly under mild reaction conditions to give the cyanomethylated products in moderate to high yields. A mechanism involving the cyanomethyl radical through C-H bond cleavage in acetonitrile was proposed. This journal is

Effects of positional and geometrical isomerism on the biological activity of some novel oxazolidinones

Das, Jagattaran,Rao, C.V. Laxman,Sastry,Roshaiah,Sankar, P. Gowri,Khadeer, Abdul,Kumar, M. Sitaram,Mallik, Arundhuti,Selvakumar,Iqbal, Javed,Trehan, Sanjay

, p. 337 - 343 (2007/10/03)

Some novel oxazolidinone derivatives have been synthesized and tested for antibacterial activity. Compound 13 was found to be active against Gram-positive pathogens whereas compound 14 was less active. Either less active or inactive molecules were obtained, when benzotriazole was replaced with benzimidazole, benzthiazole, or benzoxazole. However, thioacetamide analogue of 13 produced a potent molecule similar to linezolid in vitro. Some novel oxazolidinone derivatives with benzotriazole as pendant have been synthesized and tested for antibacterial activity. Linearly attached benzotriazole derivative showed more potency compared to angular one in vitro. Out of E/Z-isomers of angularly attached derivatives E-isomer was found to be more potent than Z-isomer. Either less active or inactive molecules were obtained, when benzotriazole was replaced with benzimidazole, benzthiazole, or benzoxazole. Finally, thioacetamide analogue of linear compound gave a lead having activity similar to linezolid in vitro.

Synthesis of polynuclear nonfused azoles

Verkhozina,Kizhnyaev,Vereshchagin,Rokhin,Smirnov

, p. 1792 - 1796 (2007/10/03)

Polynuclear blocks consisting of nonfused heterocycles of the azole series, connected through methylene bridges, were synthesized by successive addition of azole units via cycloaddition of organic azides to the triple bond of N-(2-propynyl)azoles, as well

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