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4-Benzylaminopyridine, a chemical compound with the molecular formula C12H12N2, is a derivative of pyridine that features a benzylamine group. This unique structure endows it with versatile reactivity and makes it a valuable building block in organic synthesis. Its applications span across various fields, including pharmaceutical and agrochemical research, as well as in the synthesis of pharmaceutical intermediates, dyes, and pigments. Furthermore, it has been investigated for its potential therapeutic use in Parkinson's disease, highlighting its significance in both the chemical and medical domains.

13556-71-3

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13556-71-3 Usage

Uses

Used in Chemical Synthesis:
4-Benzylaminopyridine is used as a building block in organic synthesis for its versatile reactivity, facilitating the creation of a wide range of chemical compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 4-Benzylaminopyridine is used as a catalyst in various chemical reactions, contributing to the development of new drugs and pharmaceutical intermediates.
Used in Agrochemical Research:
Similarly, in agrochemical research, 4-Benzylaminopyridine serves as a catalyst, aiding in the synthesis of compounds used in agricultural chemicals to improve crop protection and yield.
Used in Dye and Pigment Production:
4-Benzylaminopyridine is utilized in the production of dyes and pigments, where its chemical properties contribute to the color and stability of these products.
Used in Metal Scavenging:
4-Benzylaminopyridine is employed as a metal scavenger, which is crucial in removing trace metal contaminants that can interfere with sensitive chemical processes or reactions.
Used in Parkinson's Disease Research:
In the medical field, 4-Benzylaminopyridine has been studied for its potential application in the treatment of Parkinson's disease, indicating its possible role in therapeutic development for neurodegenerative conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 13556-71-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,5 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13556-71:
(7*1)+(6*3)+(5*5)+(4*5)+(3*6)+(2*7)+(1*1)=103
103 % 10 = 3
So 13556-71-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H12N2/c1-2-4-11(5-3-1)10-14-12-6-8-13-9-7-12/h1-9H,10H2,(H,13,14)

13556-71-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-benzylpyridin-4-amine

1.2 Other means of identification

Product number -
Other names 4-Benzylaminopyridine

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:13556-71-3 SDS

13556-71-3Relevant academic research and scientific papers

Design, Synthesis and Antifungal Evaluation of N-Substituted-1-(3-chloropyridin-2-yl)-N-(pyridin-4-yl)-5-(trifluoromethyl)-1H-pyrazole-4-carboxamide Derivatives

Wu, Zhibing,Yang, Guangqian,Zhao, Xin,Wu, Jiangchun,Wu, Shixi

, p. 234 - 238 (2019)

A series of 1-(3-chloropyridin-2-yl)-5-(trifluoromethyl)-1H-pyrazole-4-carboxamide derivatives which have di-substituents on nitrogen were designed and synthesized. Bioassay results showed that all the synthetic compounds exhibited lower antifungal activi

Synthesis, characterization and catalytic activity of saturated and unsaturated N-heterocyclic carbene iridium(I) complexes

Chang, Yung-Hung,Fu, Ching-Feng,Liu, Yi-Hong,Peng, Shei-Ming,Chen, Jwu-Ting,Liu, Shiuh-Tzung

, p. 861 - 867 (2009)

Both saturated and unsaturated N-benzyl substituted heterocyclic carbene (NHC) iridum(i) complexes were synthesized. The unsaturated carbene complex [(un-NHC-Bn)Ir(CO)2Cl] in the cis form was prepared via the carbene transfer from the corresponding silver complex to [Ir(COD)2Cl] 2 followed by ligand substitution with CO, whereas the saturated complex was obtained via the transfer from (sat-NHC-Bn)W(CO)5. The treatment of phosphines with (NHC)Ir(CO)2Cl complexes yielded the products with the phosphine ligand trans to the carbene moiety via substitution. X-Ray structural determination shows that distances of Ir-C(carbene) in both (un-NHC-Bn)Ir(CO)(PR3)Cl and (un-NHC-Bn)Ir(CO)(PR 3)Cl are essentially the same. Analyses of spectroscopic and crystal structural data of iridium complexes [(NHC)Ir(CO)(PR3)Cl] and Vaska's complex show similar corresponding data in both types of complexes, suggesting that the studied NHC ligands and phosphines have similar bonding with Ir(i) metal center. All iridium complexes studied in this work illustrated their catalytically activity on N-alkylation of amine with alcohol via hydrogen transfer reduction. It appears no dramatic difference on the catalytic activity among these iridium carbene complexes; but the saturated carbene complex (sat-NHC-Bn)Ir(CO)(PR3)Cl appears to be slightly more active. For example, the reaction of benzyl alcohol with aniline in the presence of catalyst (1 mol%) under basic conditions at 100 °C provided the secondary amine (N-benzylaniline) in 96% yield.

Biorenewable carbon-supported Ru catalyst for: N -alkylation of amines with alcohols and selective hydrogenation of nitroarenes

Goyal, Vishakha,Narani, Anand,Natte, Kishore,Poddar, Mukesh Kumar,Ray, Anjan,Sarki, Naina,Tripathi, Deependra

, p. 14687 - 14694 (2021/08/23)

Herein, we developed a renewable carbon-supported Ru catalyst (Ru/PNC-700), which was facilely prepared via simple impregnation followed by the pyrolysis process. The prepared Ru/PNC-700 catalyst demonstrated remarkable catalytic activity in terms of conversion and selectivity towards N-alkylation of anilines with benzyl alcohol and chemoselective hydrogenation of aromatic nitro compounds. In addition, local anesthetic pharmaceutical agents (e.g., butamben and benzocaine), including key drug intermediates, were synthesized in excellent yields under mild conditions and in the presence of water as a green solvent. Moreover, the prepared Ru/PNC-700 catalyst could be easily recovered and reused up to five times without any apparent loss in activity and selectivity.

Scalable preparation of stable and reusable silica supported palladium nanoparticles as catalysts for N-alkylation of amines with alcohols

Alshammari, Ahmad S.,Natte, Kishore,Kalevaru, Narayana V.,Bagabas, Abdulaziz,Jagadeesh, Rajenahally V.

, p. 141 - 149 (2020/01/06)

The development of nanoparticles-based heterogeneous catalysts continues to be of scientific and industrial interest for the advancement of sustainable chemical processes. Notably, up-scaling the production of catalysts to sustain unique structural features, activities and selectivities is highly important and remains challenging. Herein, we report the expedient synthesis of Pd-nanoparticles as amination catalysts by the reduction of simple palladium salt on commercial silica using molecular hydrogen. The resulting Pd-nanoparticles constitute stable and reusable catalysts for the synthesis of various N-alkyl amines using borrowing hydrogen technology without the use of any base or additive. By applying this Pd-based catalyst, functionalized and structurally diverse N-alkylated amines as well as some selected drug molecules were synthesized in good to excellent yields. Practical and synthetic utility of this Pd-based amination protocol has been demonstrated by upscaling catalyst preparation and amination reactions to several grams-scales as well as recycling of catalyst. Noteworthy, this Pd-catalyst preparation has been up-scaled to kilogram scale and catalysts prepared in both small (1 g) and large-scale (kg) exhibited similar structural features and activity.

Iridium complexes with ligands of 1,8-Naphthyridine-2-carboxylic acid derivatives-preparation and catalysis

Hsu, Yen-Pin,Li, Ming,Liu, Shiuh-Tzung,Liu, Yi-Hung,Peng, Shie-Ming

, (2020/10/02)

Complexation of 1,8-naphthyridine(Np)-2-carboxylic derivatives L1-L3 [L1 = Np-2-COOH, L2 = Np-2-CONH2, L3 = Np-2-CONHCH2Py] with [Ir(COD)(μ-OMe)]2 yielded the corresponding complexes [Ir(COD)(Ln)] (1~3, n = 1~3, respectively). The potential tridentate L3 behaves as a bidentate donor in the complex 3. Treatment of L1 with [Ir(COD)Cl]2 under nitrogen atmosphere gave a Ir(III) hydride complex [Ir(COD)(L1)HCl] (4). However, carrying out the reaction in the presence of oxygen rendered a Ir(III) dichloride species [Ir(COD)(L1)Cl2] (5). All these complexes were characterized by spectroscopic analyses and X-ray single crystal determination. Catalytic activity of iridium complexes in amination of amines with alcohols was screened. It appears that iridium amido complexes 2 and 3 show excellent catalytic activity on amination of anilines with alcohols in the presence of Cs2CO3 at 120 °C.

Bidentate geometry-constrained iminopyridyl nickel-catalyzed synthesis of amines or imines via borrowing hydrogen or dehydrogenative condensation

Jiang, Yong,Hu, Miao,Sun, Nan,Hu, Baoxiang,Shen, Zhenlu,Hu, Xinquan,Jin, Liqun

supporting information, (2020/11/27)

The efficient Ni-catalyzed N-alkylation of various anilines with alcohols via borrowing hydrogen is reported using a bidentate geometry-constrained iminopyridyl nickel complex as the catalyst. Substituted benzylic alcohols and short/long chain aliphatic alcohols could be applied as the alkylation sources to couple with aromatic and heteroaromatic amines to give a diverse set of N-alkylation outcomes in moderate to excellent yields. The nickel catalytic system was also suitable for aliphatic amines, selectively delivering the corresponding imines via an acceptorless dehydrogenative condensation strategy.

Solvent-Free N-Alkylation and Dehydrogenative Coupling Catalyzed by a Highly Active Pincer-Nickel Complex

Arora, Vinay,Dutta, Moumita,Das, Kanu,Das, Babulal,Srivastava, Hemant Kumar,Srivastava, Hemant Kumar,Kumar, Akshai,Kumar, Akshai

, p. 2162 - 2176 (2020/06/05)

The synthesis and characterization of a pincer-nickel complex of the type (iPr2NNN)NiCl2(CH3CN) is reported here. We have demonstrated the utility of this pincer-nickel complex (0.02 and 0.002 mol %) for the catalytic N-alkylation of amines using various alcohols. Under solvent-free conditions, while the highest yield (ca. 90%) was obtained for the alkylation of 2-aminopyridine with naphthyl-1-methanol, excellent turnovers (34000 TONs) were observed for the alkylation of 2-aminopyridine with 4-methoxybenzyl alcohol. To demonstrate the synthetic utility of these systems, high-yield reactions (up to 98%) have been probed for representative substrates with a higher loading of the pincer-nickel catalyst (4 mol %). DFT studies indicate that while β-hydride elimination is the RDS for alcohol dehydrogenation, the N-alkylated product can be formed either via hydrogenation with a rate-determining σ-bond metathesis or by alcoholysis that has imine insertion as the RDS. All of the corresponding resting states have been observed by HRMS (ESI) analysis. The labeling experiments are also complementary to DFT studies and show evidence for the involvement of the benzylic C-H bond in the RDS with a kCHH/kCHD value of about 2.5. This method has been applied to accomplish efficient (2000 TONs) dehydrogenative coupling leading to various benzimidazoles.

Selective Synthesis of Secondary Amines from Nitriles by a User-Friendly Cobalt Catalyst

Sharma, Dipesh M.,Punji, Benudhar

supporting information, p. 3930 - 3936 (2019/07/12)

Selective hydrogenation/reductive amination of nitriles to secondary amines catalyzed by an inexpensive and user-friendly cobalt complex, (Xantphos)CoCl2, is reported. The use of (Xantphos)CoCl2 and ammonia borane (NH3?BH3) combination affords the selective reduction of nitriles to symmetrical secondary amines, whereas the employment of (Xantphos)CoCl2 and dimethylamine borane (Me2NH?BH3) along with external amines produce unsymmetrical secondary amines and tertiary amines. The general applicability of this methodology is demonstrated by the synthesis of 43 symmetrical and unsymmetrical secondary and tertiary amines bearing diverse functionalities. (Figure presented.).

Borrowing Hydrogen-Mediated N-Alkylation Reactions by a Well-Defined Homogeneous Nickel Catalyst

Bains, Amreen K.,Kundu, Abhishek,Yadav, Sudha,Adhikari, Debashis

, p. 9051 - 9059 (2019/10/02)

We report herein a well-defined and bench-stable azo-phenolate ligand-coordinated nickel catalyst which can efficiently execute N-alkylation of a variety of anilines by alcohol. We demonstrate that the redox-active azo ligand can store hydrogen generated during alcohol oxidation and redelivers the same to an in-situ-generated imine bond to result in N-alkylation of amines. The reaction has wide scope, and a large array of alcohols can directly couple to a variety of anilines. Mechanistic studies including deuterium labeling to the substrate establishes the borrowing hydrogen method from alcohols and pinpoints the crucial role of the redox-active azo moiety present on the ligand backbone. Isolation of the ketyl intermediate in its trapped form with a radical quencher and higher kH/kD for the alcohol oxidation step suggest altogether a hydrogen-atom transfer (HAT) to the reduced azo backbone to pave alcohol oxidation as opposed to the conventional metal-ligand bifunctional mechanism. This example clearly demonstrates that an inexpensive base metal catalyst can accomplish an important coupling reaction with the help of a redox-active ligand backbone.

Preparation of the Ru3(CO)8-pyridine-alcohol cluster and its use for the selective catalytic transformation of primary to secondary amines

Singh, Ajeet,Mobin, Shaikh M.,Mathur, Pradeep

, p. 14033 - 14040 (2018/11/23)

The synthesis of pyridine alcohol based ruthenium carbonyl clusters Ru3(hep)2(CO)8 (1), Ru3(hpp)2(CO)8 (2), and Ru3(bhmp-H)2(CO)8 (3) {hep-H = 2-(2-hydroxyethyl)pyridine, hpp-H = 2-(3-hydroxypropyl)pyridine and bhmp-H2 = 2,6-bis(hydroxymethyl)pyridine} has been carried out by the reaction of the corresponding pyridine-alcohol ligands with Ru3(CO)12. Clusters 1-3 have been characterized using elemental analysis, NMR, FT-IR, mass spectrometry and single-crystal X-ray structures. The clusters were explored for the selective catalytic transformation of primary amines into secondary amines using alcohols as the mono-alkylating agents via hydrogen transfer reactions. All three display efficient catalytic activity with 1 being the most effective.

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