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2-Pyridinemethanol, α-(2-methoxyphenyl)-, also known as 2-(2-methoxyphenyl)pyridine-2-methanol or 2-(2-methoxyphenyl)-2-pyridinemethanol, is an organic compound with the chemical formula C12H13NO2. It is a derivative of pyridine, featuring a methanol group attached to the 2-position of the pyridine ring and a 2-methoxyphenyl group at the α-position. 2-Pyridinemethanol, a-(2-methoxyphenyl)- is a white crystalline solid and is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. It is characterized by its unique chemical structure, which combines the properties of both pyridine and phenol, making it a versatile building block in organic chemistry.

27652-91-1

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27652-91-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27652-91-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,6,5 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 27652-91:
(7*2)+(6*7)+(5*6)+(4*5)+(3*2)+(2*9)+(1*1)=131
131 % 10 = 1
So 27652-91-1 is a valid CAS Registry Number.

27652-91-1SDS

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 2-(hydroxy(pyridin-2-yl)methyl)methoxybenzene

1.2 Other means of identification

Product number -
Other names (2-Methoxy-phenyl)-[2]pyridyl-methanol

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:27652-91-1 SDS

27652-91-1Relevant academic research and scientific papers

Ligand-Free Iridium-Catalyzed Dehydrogenative ortho C?H Borylation of Benzyl-2-Pyridines at Room Temperature

Yang, Yuhuan,Gao, Qian,Xu, Senmiao

supporting information, p. 858 - 862 (2019/01/04)

A convenient and ligand-free iridium-catalyzed dehydrogenative ortho C?H borylation of benzyl-2-pyridines has been developed. The reaction proceeds smoothly at room temperature using pinacolborane as a borylating reagent in the presence of catalytic amount of [IrOMe(COD)]2. The reaction is compatible with many functional groups, providing a vast array of ortho borylated products in moderate to excellent yields with excellent selectivities. (Figure presented.).

Chiral organomagnesiates as dual reagents for bromine-magnesium exchange of 2-bromopyridine and access to chiral α-substituted 2-pyridylcarbinols

Catel, Delphine,Chevallier, Floris,Mongin, Florence,Gros, Philippe C.

supporting information; experimental part, p. 53 - 57 (2012/02/06)

New chiral ligand containing butyl and dibutylmagnesiates have been prepared from a range of ligands and their reactivity studied. The reagents were generally efficient in promoting the clean bromine-magnesium exchange of 2-bromopyridine at room temperature and the subsequent reaction with aldehydes to afford α-substituted 2-pyridylcarbinols in good yields. (R,R)-TADDOLate proved to be the best ligand, leading to acceptable to good enantioselectivities. To the best of our knowledge this is the first example of an organomagnesiate-induced halogen-metal exchange followed by an enantioselective addition.

Pyridylmagnesiates: Generation by bromine-metal exchange and enantioselective addition to aldehydes

Catel, Delphine,Payen, Olivier,Chevallier, Floris,Mongin, Florence,Gros, Philippe C.

experimental part, p. 4018 - 4028 (2012/07/28)

Butyl and dibutylmagnesiates incorporating chiral ligands have been prepared and their reactivity studied. The reagents were efficient to promote the clean bromine-magnesium exchange of azinyl bromides at room temperature and subsequent reaction with aldehydes affording pyridylcarbinols. (R,R)-TADDOL-based dibutylmagnesiate was the best reagent leading to acceptable to good enantioselectivities, depending on the substrate and on the aldehyde substitution. This is the first example of enantioselective addition of in situ generated pyridylmagnesiate to carbonyl electrophiles.

[1,2]-Wittig rearrangement of aromatic heterocycles

Yang, Jingyue,Wangweerawong, Apiwat,Dudley, Gregory B.

scheme or table, p. 1603 - 1606 (2012/08/29)

Anionic rearrangement of diverse heteroaryl ethers is reported. In many cases, directed metallation followed by formal [1,2]-Wittig rearrangement provides heteroaryl carbinols in good yield.

Highly flexible O,O′,N ligands and their Fe, Ni, Cu and Zn complexes

Butsch, Katharina,Klein, Axel,Bauer, Matthias

experimental part, p. 350 - 358 (2011/09/16)

Three new chiral ligands bearing an O,O′,N donor set (O methoxyOhydroxyNpyridine) were synthesised and coordinated to FeIII, FeII, NiII, Cu II and ZnII to yield complexes with the general formula [M(OON)Clx]y. While the pyridine N and the hydroxy O atoms coordinate strongly to all applied metal ions, the methoxy donor seems not to be involved in coordination, although some evidence for a weak interaction between OMe and the ZnII were found in NMR spectra. In the bidentate O′,N coordination mode the new ligands exhibit several coordination geometries as analysed in the solid compounds by XRD, EXAFS and EPR and in solution by UV-Vis absorption, cyclic voltammetry, EXAFS, EPR or NMR spectroscopy.

[1,2]-Anionic rearrangement of 2-benzyloxypyridine and related pyridyl ethers

Yang, Jingyue,Dudley, Gregory B.

supporting information; experimental part, p. 7998 - 8000 (2010/03/01)

(Chemical Equation Presented) An anionic rearrangement of 2-benzyloxypyridine is described. Pyridine-directed metalation of the benzylic carbon leads to 1,2-migration of pyridine via a postulated associative mechanism (addition/elimination). Several aryl pyridyl carbinols were obtained in high yields. A formal synthesis of carbinoxamine, an antihistamine drug used for the treatment of seasonal allergies and hay fever, emerges from this methodology.

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