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1-Pyridin-4-yl-ethanol, also known as 4-(Hydroxymethyl)pyridine, is a chemical compound characterized by the molecular formula C7H9NO. This colorless, viscous liquid serves as a crucial intermediate in the synthesis of a variety of pharmaceuticals, pesticides, and other organic compounds. Its versatile nature as a building block in the production of drugs, including antihistamines, antipsychotics, and analgesics, underscores its importance in the pharmaceutical and agrochemical industries.

42732-22-9

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42732-22-9 Usage

Uses

Used in Pharmaceutical Industry:
1-Pyridin-4-yl-ethanol is used as a chemical intermediate for the synthesis of various drugs, such as antihistamines, antipsychotics, and analgesics, due to its ability to facilitate the creation of complex molecular structures that address specific medical needs.
Used in Agrochemical Industry:
1-Pyridin-4-yl-ethanol is used as a precursor in the development of pesticides, contributing to the production of effective and targeted agricultural chemicals that protect crops and enhance yields.
Used in Organic Chemical Reactions:
1-Pyridin-4-yl-ethanol is utilized as a solvent and reagent in organic chemical reactions, enabling the synthesis of a range of organic compounds for diverse applications, from pharmaceuticals to specialty chemicals.
Although 1-Pyridin-4-yl-ethanol has limited direct applications, its role as a versatile intermediate in the synthesis of various compounds makes it an indispensable component in the development of new and improved products across multiple industries.

Check Digit Verification of cas no

The CAS Registry Mumber 42732-22-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,7,3 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 42732-22:
(7*4)+(6*2)+(5*7)+(4*3)+(3*2)+(2*2)+(1*2)=99
99 % 10 = 9
So 42732-22-9 is a valid CAS Registry Number.
InChI:InChI=1S/C7H9NO/c1-6(9)7-2-4-8-5-3-7/h2-6,9H,1H3

42732-22-9 Well-known Company Product Price

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  • Alfa Aesar

  • (H58711)  4-(1-Hydroxyethyl)pyridine, 97%   

  • 42732-22-9

  • 5g

  • 1092.0CNY

  • Detail
  • Alfa Aesar

  • (H58711)  4-(1-Hydroxyethyl)pyridine, 97%   

  • 42732-22-9

  • 30g

  • 4368.0CNY

  • Detail
  • Aldrich

  • (82904)  (±)-α-Methyl-4-pyridinemethanol  ≥98.0% (GC)

  • 42732-22-9

  • 82904-10G

  • 2,469.87CNY

  • Detail

42732-22-9SDS

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 4-(1-Hydroxyethyl)pyridine

1.2 Other means of identification

Product number -
Other names (±)-α-Methyl-4-pyridinemethanol

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:42732-22-9 SDS

42732-22-9Relevant academic research and scientific papers

Cinchona-Alkaloid-Derived NNP Ligand for Iridium-Catalyzed Asymmetric Hydrogenation of Ketones

Zhang, Lin,Zhang, Ling,Chen, Qian,Li, Linlin,Jiang, Jian,Sun, Hao,Zhao, Chong,Yang, Yuanyong,Li, Chun

supporting information, p. 415 - 419 (2022/01/12)

Most ligands applied for asymmetric hydrogenation are synthesized via multistep reactions with expensive chemical reagents. Herein, a series of novel and easily accessed cinchona-alkaloid-based NNP ligands have been developed in two steps. By combining [Ir(COD)Cl]2, 39 ketones including aromatic, heteroaryl, and alkyl ketones have been hydrogenated, all affording valuable chiral alcohols with 96.0-99.9% ee. A plausible reaction mechanism was discussed by NMR, HRMS, and DFT, and an activating model involving trihydride was verified.

Ni2P Nanoalloy as an Air-Stable and Versatile Hydrogenation Catalyst in Water: P-Alloying Strategy for Designing Smart Catalysts

Fujita, Shu,Yamaguchi, Sho,Yamasaki, Jun,Nakajima, Kiyotaka,Yamazoe, Seiji,Mizugaki, Tomoo,Mitsudome, Takato

supporting information, p. 4439 - 4446 (2021/02/09)

Non-noble metal-based hydrogenation catalysts have limited practical applications because they exhibit low activity, require harsh reaction conditions, and are unstable in air. To overcome these limitations, herein we propose the alloying of non-noble metal nanoparticles with phosphorus as a promising strategy for developing smart catalysts that exhibit both excellent activity and air stability. We synthesized a novel nickel phosphide nanoalloy (nano-Ni2P) with coordinatively unsaturated Ni active sites. Unlike conventional air-unstable non-noble metal catalysts, nano-Ni2P retained its metallic nature in air, and exhibited a high activity for the hydrogenation of various substrates with polar functional groups, such as aldehydes, ketones, nitriles, and nitroarenes to the desired products in excellent yields in water. Furthermore, the used nano-Ni2P catalyst was easy to handle in air and could be reused without pretreatment, providing a simple and clean catalyst system for general hydrogenation reactions.

Reduction of carbonyl compounds via hydrosilylation catalyzed by well-defined PNP-Mn(I) hydride complexes

Weber, Stefan,Iebed, Dina,Glatz, Mathias,Kirchner, Karl

, p. 635 - 639 (2021/06/17)

Reduction reactions of unsaturated compounds are fundamental transformations in synthetic chemistry. In this context, the reduction of polarized double bonds such as carbonyl or C=C motifs can be achieved by hydrogenation reactions. We describe here a highly chemoselective Mn(I)-based PNP pincer catalyst for the hydrosilylation of aldehydes and ketones employing polymethylhydrosiloxane (PMHS) as inexpensive hydrogen donor. Graphic abstract: [Figure not available: see fulltext.]

Dynamic Kinetic Resolution of Alcohols by Enantioselective Silylation Enabled by Two Orthogonal Transition-Metal Catalysts

Oestreich, Martin,Seliger, Jan

supporting information, p. 247 - 251 (2020/10/29)

A nonenzymatic dynamic kinetic resolution of acyclic and cyclic benzylic alcohols is reported. The approach merges rapid transition-metal-catalyzed alcohol racemization and enantioselective Cu-H-catalyzed dehydrogenative Si-O coupling of alcohols and hydrosilanes. The catalytic processes are orthogonal, and the racemization catalyst does not promote any background reactions such as the racemization of the silyl ether and its unselective formation. Often-used ruthenium half-sandwich complexes are not suitable but a bifunctional ruthenium pincer complex perfectly fulfills this purpose. By this, enantioselective silylation of racemic alcohol mixtures is achieved in high yields and with good levels of enantioselection.

Manganese-Catalyzed Hydrogenation of Ketones under Mild and Base-free Conditions

Brünig, Julian,Kirchner, Karl,Veiros, Luis F.,Weber, Stefan

supporting information, p. 1388 - 1394 (2021/05/31)

In this paper, several Mn(I) complexes were applied as catalysts for the homogeneous hydrogenation of ketones. The most active precatalyst is the bench-stable alkyl bisphosphine Mn(I) complex fac-[Mn(dippe) (CO)3(CH2CH2CH3)]. The reaction proceeds at room temperature under base-free conditions with a catalyst loading of 3 mol % and a hydrogen pressure of 10 bar. A temperature-dependent selectivity for the reduction of α,β-unsaturated carbonyls was observed. At room temperature, the carbonyl group was selectively hydrogenated, while the C=C bond stayed intact. At 60 °C, fully saturated systems were obtained. A plausible mechanism based on DFT calculations which involves an inner-sphere hydride transfer is proposed.

Manganese-catalyzed homogeneous hydrogenation of ketones and conjugate reduction of α,β-unsaturated carboxylic acid derivatives: A chemoselective, robust, and phosphine-free in situ-protocol

Topf, Christoph,Vielhaber, Thomas

, (2021/07/10)

We communicate a user-friendly and glove-box-free catalytic protocol for the manganese-catalyzed hydrogenation of ketones and conjugated C[dbnd]C[sbnd]bonds of esters and nitriles. The respective catalyst is readily assembled in situ from the privileged [Mn(CO)5Br] precursor and cheap 2-picolylamine. The catalytic transformations were performed in the presence of t-BuOK whereby the corresponding hydrogenation products were obtained in good to excellent yields. The described system offers a brisk and atom-efficient access to both secondary alcohols and saturated esters avoiding the use of oxygen-sensitive and expensive phosphine-based ligands.

Amino Acid-Functionalized Metal-Organic Frameworks for Asymmetric Base–Metal Catalysis

Newar, Rajashree,Akhtar, Naved,Antil, Neha,Kumar, Ajay,Shukla, Sakshi,Begum, Wahida,Manna, Kuntal

, p. 10964 - 10970 (2021/03/29)

We report a strategy to develop heterogeneous single-site enantioselective catalysts based on naturally occurring amino acids and earth-abundant metals for eco-friendly asymmetric catalysis. The grafting of amino acids within the pores of a metal-organic framework (MOF), followed by post-synthetic metalation with iron precursor, affords highly active and enantioselective (>99 % ee for 10 examples) catalysts for hydrosilylation and hydroboration of carbonyl compounds. Impressively, the MOF-Fe catalyst displayed high turnover numbers of up to 10 000 and was recycled and reused more than 15 times without diminishing the enantioselectivity. MOF-Fe displayed much higher activity and enantioselectivity than its homogeneous control catalyst, likely due to the formation of robust single-site catalyst in the MOF through site-isolation.

Chiral Iron(II)-Catalysts within Valinol-Grafted Metal-Organic Frameworks for Enantioselective Reduction of Ketones

Akhtar, Naved,Antil, Neha,Begum, Wahida,Chauhan, Manav,Kumar, Ajay,Manna, Kuntal,Newar, Rajashree

, p. 10450 - 10459 (2021/08/31)

The development of highly efficient and enantioselective heterogeneous catalysts based on earth-abundant elements and inexpensive chiral ligands is essential for environment-friendly and economical production of optically active compounds. We report a strategy of synthesizing chiral amino alcohol-functionalized metal-organic frameworks (MOFs) to afford highly enantioselective single-site base-metal catalysts for asymmetric organic transformations. The chiral MOFs (vol-UiO) were prepared by grafting of chiral amino alcohol such as l-valinol within the pores of aldehyde-functionalized UiO-MOFs via formation of imine linkages. The metalation of vol-UiO with FeCl2 in THF gives amino alcohol coordinated octahedral FeII species of vol-FeCl(THF)3 within the MOFs as determined by X-ray absorption spectroscopy. Upon activation with LiCH2SiMe3, vol-UiO-Fe catalyzed hydrosilylation and hydroboration of a range of aliphatic and aromatic carbonyls to afford the corresponding chiral alcohols with enantiomeric excesses up to 99%. Vol-UiO-Fe catalysts have high turnover numbers of up to 15 ?000 and could be reused at least 10 times without any loss of activity and enantioselectivity. The spectroscopic, kinetic, and computational studies suggest iron-hydride as the catalytic species, which undergoes enantioselective 1,2-insertion of carbonyl to give an iron-alkoxide intermediate. The subsequent σ-bond metathesis between Fe-O bond and Si-H bond of silane produces chiral silyl ether. This work highlights the importance of MOFs as the tunable molecular material for designing chiral solid catalysts based on inexpensive natural feedstocks such as chiral amino acids and base-metals for asymmetric organic transformations.

Ruthenium-catalyzed hydrogenation of aromatic ketones using chiral diamine and monodentate achiral phosphine ligands

Wang, Mengna,Zhang, Ling,Sun, Hao,Chen, Qian,Jiang, Jian,Li, Linlin,Zhang, Lin,Li, Li,Li, Chun

, (2021/03/24)

The Ru-catalyzed asymmetric hydrogenation of ketones with chiral diamine and monodentate achiral phosphine has been developed. A wide range of ketones were hydrogenated to afford the corresponding chiral secondary alcohols in good to excellent enantioselectivities (up to 98.1% ee). In addition, an appropriate mechanism for the asymmetric hydrogenation was proposed and verified by NMR spectroscopy.

Ferrocene derivative metal organic complex as well as preparation method and application thereof

-

Paragraph 0147-0157, (2021/12/07)

The invention relates to the technical field of organic synthesis, in particular to a ferrocene derivative metal organic complex and a preparation method and application thereof. The ferrocene derivative metal organic complex disclosed by the invention is shown I, contains a pincerlike ligand in the structure, and therefore has high stability and long service life. , The ferrocene derivative type metal organic complex has high catalytic activity, and only 0.001 μM % - 0.01 μM % is used, so that the chiral compound can be efficiently and rapidly prepared. The ferrocene derivative metal organic complex central metal is ruthenium, the economic cost is low, and the method has the prospect of industrial popularization.

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