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2,3-Dichloroaniline is an organic compound with the chemical formula C6H4Cl2NH2, featuring a chlorine atom attached to both the 2nd and 3rd positions of the aniline molecule. It is a colorless to pale yellow crystalline solid with a strong, irritating odor. This chemical is known for its reactivity and is commonly used as an intermediate in the synthesis of various organic compounds.

608-27-5

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608-27-5 Usage

Uses

Used in Dye and Pigment Industry:
2,3-Dichloroaniline is used as a chemical intermediate for the production of dyes and pigments, which are essential for coloring textiles, plastics, and other materials. Its presence in these compounds contributes to their color intensity and stability.
Used in Optical Brighteners Industry:
In the optical brighteners industry, 2,3-dichloroaniline is utilized as a precursor for the synthesis of fluorescent whitening agents. These agents enhance the appearance of materials by reflecting light more efficiently, giving them a brighter and more vivid look.
Used in Flame Retardants Industry:
2,3-Dichloroaniline is used as a flame retardant for polymers, helping to reduce the flammability of various materials. This application is crucial in industries such as construction, electronics, and automotive, where fire safety is a significant concern.
Used in Agricultural Chemicals Industry:
In the agricultural chemicals industry, 2,3-dichloroaniline is used in the manufacturing of growth regulators. These regulators are essential for controlling plant growth and development, leading to improved crop yields and quality.
Used in Polymer Auxiliaries Industry:
2,3-Dichloroaniline is also used in the production of polymer auxiliaries, which are additives that improve the properties of polymers during their synthesis and processing. These auxiliaries can enhance the strength, flexibility, and durability of the final polymer products.

Check Digit Verification of cas no

The CAS Registry Mumber 608-27-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,0 and 8 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 608-27:
(5*6)+(4*0)+(3*8)+(2*2)+(1*7)=65
65 % 10 = 5
So 608-27-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H5Cl2N/c7-4-2-1-3-5(9)6(4)8/h1-3H,9H2

608-27-5 Well-known Company Product Price

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  • Alfa Aesar

  • (A11524)  2,3-Dichloroaniline, 99%   

  • 608-27-5

  • 100g

  • 313.0CNY

  • Detail
  • Alfa Aesar

  • (A11524)  2,3-Dichloroaniline, 99%   

  • 608-27-5

  • 500g

  • 860.0CNY

  • Detail
  • Alfa Aesar

  • (A11524)  2,3-Dichloroaniline, 99%   

  • 608-27-5

  • 2500g

  • 3620.0CNY

  • Detail
  • Sigma-Aldrich

  • (36701)  2,3-Dichloroaniline  PESTANAL®, analytical standard

  • 608-27-5

  • 36701-1G

  • 193.05CNY

  • Detail

608-27-5SDS

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 2,3-dichloroaniline

1.2 Other means of identification

Product number -
Other names Aniline,2,3-dichloro

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:608-27-5 SDS

608-27-5Relevant academic research and scientific papers

N-Functionalised Imidazoles as Stabilisers for Metal Nanoparticles in Catalysis and Anion Binding

Beer, Paul D.,Cookson, James,Serpell, Christopher J.

, p. 683 - 690 (2020/07/03)

Metal nanoparticles (NPs) have physicochemical properties which are distinct from both the bulk and molecular metal species, and provide opportunities in fields such as catalysis and sensing. NPs typically require protection of their surface to impede aggregation, but these coatings can also block access to the surface which would be required to take advantage of their unusual properties. Here, we show that alkyl imidazoles can stabilise Pd, Pt, Au, and Ag NPs, and delineate the limits of their synthesis. These ligands provide an intermediate level of surface protection, for which we demonstrate proof-of-principle in catalysis and anion binding.

Selective hydrogenation of nitroarenes under mild conditions by the optimization of active sites in a well defined Co?NC catalyst

Chen, Shuo,Jiang, Hong,Jiang, Shun-Feng,Ling, Li-Li

, p. 5730 - 5741 (2020/09/21)

The catalytic hydrogenation of aromatic nitro compounds containing multiple functional groups into amino compounds with high conversion rates, selectivity, and stability under mild conditions is a great challenge. Herein, a well defined catalyst (Co?NC) is prepared through the pyrolysis of the Co-centered metal-organic framework (MOF) at the optimized temperature. The as-synthesized catalyst exhibits a high conversion rate and selectivity for the hydrogenation of 12 aromatic nitro compounds with different competing groups into desired amino compounds with hydrazine hydrate under mild conditions (80 °C, 30 min, and 1 atm). The catalyst also shows excellent stability and can be reused over 20 times without considerably losing its activity. It is found that the Co-Nx site is the main active site for catalytic hydrogenation, and the Mott-Schottky effect between the surface Co NPs and N-doped carbon can further promote the hydrogenation reaction. EXAFS, TEM, XPS, and Raman analyses confirm that cobalt nanoparticles (NPs) are properly encapsulated by the N-doped carbon matrix at the optimized temperature, and the Co species maintain a high spin state after the catalysis, which may be responsible for the high performance of Co?NC. This work demonstrates not only a highly efficient catalyst for hydrogenation under mild conditions, but also provides insight into the active sites in Co-based catalysts for hydrogenation.

Site-Selective Copper-Catalyzed Amination and Azidation of Arenes and Heteroarenes via Deprotonative Zincation

Hendrick, Charles E.,Bitting, Katie J.,Cho, Seoyoung,Wang, Qiu

, p. 11622 - 11628 (2017/08/30)

Arene amination is achieved by site-selective C-H zincation followed by copper-catalyzed coupling with O-benzoylhydroxylamines under mild conditions. Key to this success is ortho-zincation mediated by lithium amidodiethylzincate base that is effective for a wide range of arenes, including nonactivated arenes bearing simple functionalities such as fluoride, chloride, ester, amide, ether, nitrile, and trifluoromethyl groups as well as heteroarenes including indole, thiophene, pyridine, and isoquinoline. An analogous C-H azidation is also accomplished using azidoiodinane for direct introduction of a useful azide group onto a broad scope of arenes and heteroarenes. These new transformations offer rapid access to valuable and diverse chemical space of aminoarenes. Their broad applications in organic synthesis and drug discovery are demonstrated in the synthesis of novel analogues of natural product (-)-nicotine and antidepressant sertraline by late-stage amination and azidation reactions.

Perovskite-type ferromagnetic BiFeO3 nanopowder: A new magnetically recoverable heterogeneous nanocatalyst for efficient and selective transfer hydrogenation of aromatic nitro compounds into aromatic amines under microwave heating

Farhadi,Rashidi

, p. 1021 - 1031 (2013/02/23)

Perovskite-type ferromagnetic BiFeO3 nanopowder was readily synthesized via thermal decomposition of Bi[Fe(CN)6].5H2O complex and characterized using thermal analysis (TGA/DSC), X-ray diffraction (XRD), Fourier-transformed infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDX), magnetic measurement and Brunauer-Emmett- Teller (BET) specific surface area measurements. The magnetic measurements show a ferromagnetic behavior for the BiFeO3 nanoparticles at room temperature. This nanosized ferromagnetic oxide with an average particle size of approximately 20 nm and a specific surface area of 48.5 m2/g was used as a new magnetically recoverable heterogeneous nanocatalyst for the highly efficient and selective reduction of aromatic nitro compounds into their corresponding amines by using propan-2-ol as the hydrogen donor under microwave irradiation. This method is regio- and chemoselective, clean, inexpensive and compatible with the substrates having hydrogenlyzable or reducible functional groups. As compared with conventional heating, this method is very fast and suitable for the large-scale preparation of different substituted anilines as well as other arylamines. The catalyst can also be reused without loss of activity. Iranian Chemical Society 2012.

Novel approach for the synthesis of N-Substituted pyrroles starting directly from nitro compounds in water

Das, Biswanath,Shinde, Digambar Balaji,Kanth, Boddu Shashi,Kumar, Jayprakash Narayan

experimental part, p. 548 - 553 (2011/11/29)

A novel approach for a facile high-yielding synthesis of N-substituted pyrroles has been discovered by the treatment of nitroarenes with 2,5-dimethoxytetrahydrofuran using indium in dilute aqueous HCl at room temperature. Taylor & Francis Group, LLC.

Approaches to the synthesis of 2,3-dihaloanilines. Useful precursors of 4-functionalized-1 H-indoles

Guilarte, Veronica,Castroviejo, M. Pilar,Garcia-Garcia, Patricia,Fernandez-Rodriguez, Manuel A.,Sanz, Roberto

experimental part, p. 3416 - 3437 (2011/06/28)

2,3-Dihaloanilines have been proved as useful starting materials for synthesizing 4-halo-1H-indoles. Subsequent or in situ functionalization of the prepared haloindoles allows the access to a wide variety of 2,4- or 2,3,4-regioselectively functionalized indoles in good overall yields. As no efficient synthetic routes to 2,3-dihaloanilines have been described in the literature, different approaches to the preparation of these 1,2,3-functionalized aromatic precursors are now presented. The most general one involves a Smiles rearrangement from the corresponding 2,3-dihalophenols and allows the preparation of 2,3-dihaloanilides in a straightforward and synthetically useful manner.

NiO nanoparticles prepared via thermal decomposition of the bis(dimethylglyoximato)nickel(II) complex: A novel reusable heterogeneous catalyst for fast and efficient microwave-assisted reduction of nitroarenes with ethanol

Farhadi, Saeid,Kazem, Maryam,Siadatnasab, Firouzeh

scheme or table, p. 606 - 613 (2011/04/16)

NiO nanoparticles with an average size of 12 nm and a high specific surface area of 88.5 m2/g were easily prepared via the thermal decomposition of the complex Ni(dmgH)2 and were characterized by TGA, XRD, FT-IR, TEM and BET surface area measurement. This nanosized transition metal oxide was used as a new heterogeneous catalyst for the reduction of nitroarenes under microwave irradiation. The efficient and selective reduction of aromatic nitro compounds into their corresponding amines was observed by using ethanol as a hydrogen donor (reducing agent) and KOH as a promoter under microwave irradiation. This highly regio-and chemoselective method is fast, simple, inexpensive, high yielding, clean and compatible with several sensitive functionalities, such as halogens,-OH,-OCH3,-CHO,-COCH 3,-COOH,-COOEt,-CONH2,-CN,-CHCH2 and-NHCOCH3. This method is suitable for the large scale preparation of different substituted anilines as well as other arylamines. In addition, the catalytic activity of nanosized NiO is higher than that of the bulk sample.

Perovskite-type LaFeO3 nanoparticles prepared by thermal decomposition of the La[Fe(CN)6]·5H2O complex: A new reusable catalyst for rapid and efficient reduction of aromatic nitro compounds to arylamines with propan-2-ol under microwave irradiation

Farhadi, Saeid,Siadatnasab, Firouzeh

experimental part, p. 108 - 116 (2011/05/19)

Perovskite-type LaFeO3 nanoparticles were readily synthesized via thermal decomposition of the La[Fe(CN)6]·5H2O complex and characterized by using thermal analysis (TGA), X-ray diffraction (XRD), Fourier-transformed infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), transmission electron microscopy (TEM) and BET specific surface area measurement. This nanosized perovskite-type oxide with an average particle size of 35 nm and a specific surface area 38.5 m2/g was used as a new reusable heterogeneous catalyst for highly efficient and selective reduction of aromatic nitro compounds into their corresponding amines by using propan-2-ol as the hydrogen donor under microwave irradiation. This method is regio- and chemoselective, clean, inexpensive and compatible with the substrates having hydrogenlysable or reducible functional groups. As compared with conventional heating, this method is very fast and suitable for large scale preparation of different substituted anilines as well as other arylamines. The catalyst can also be reused without observable loss of its activity.

Microwave-assisted rapid and efficient reduction of aromatic nitro compounds to amines with propan-2-ol over Nanosized perovskite-type SmFeO 3 powder as a new recyclable heterogeneous catalyst

Farhadi, Saeid,Siadatnasab, Firouzeh,Kazem, Maryam

experimental part, p. 104 - 108 (2011/06/27)

Nanosized perovskite-type SmFeO3 powder, prepared through the thermal decomposition of Sm[Fe(CN)6].4H2O with an average particle diameter of 28 nm and a specific surface area of 42 m2 g-1, was used as a recyclable heterogeneous catalyst for the efficient and selective reduction of aromatic nitro compounds into the corresponding amines by using propan-2-ol as a hydrogen donor (reducing agent) and KOH as a promoter under microwave irradiation. This highly regio-and chemoselective catalytic method is fast, clean, inexpensive, high yielding and also compatible with the substrates containing easily reducible functional groups. In addition, the nanosized SmFeO3 catalyst can be reused without loss of activity.

Hydrous zirconia supported iridium nanoparticles: An excellent catalyst for the hydrogenation of haloaromatic nitro compounds

Fan, Guang-Yin,Zhang, Lei,Fu, Hai-Yan,Yuan, Mao-Lin,Li, Rui-Xiang,Chen, Hua,Li, Xian-Jun

scheme or table, p. 451 - 455 (2010/11/21)

Ir/ZrO2·xH2O was prepared by co-precipitation and characterized by TEM, XRD, and XPS. It showed an excellent catalytic performance for the hydrogenation of haloaromatic nitro compounds to the corresponding amines in the mixture solvent of ethanol and water. The catalyst gave both conversion and selectivity to be over 99.9% for the hydrogenation of p-chloronitrobenzene to p-chloroaniline. Besides the intrinsic characterization of iridium in the hydrogenation of haloaromatic nitro compounds, the high activity and selectivity of Ir/ZrO2·xH2O is probably attributed to the formation of hydrogen bond between substrate and the hydroxyl groups on the surface of the hydrous catalyst or solvent water to activate the N{double bond, long}O bond in nitro group. The activated N{double bond, long}O bond is easy to be attacked by the activated hydrogen, so the hydrogenation is promoted.

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