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Pyridine, 3,6-dimethyl-2-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

27068-69-5

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27068-69-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27068-69-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,0,6 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 27068-69:
(7*2)+(6*7)+(5*0)+(4*6)+(3*8)+(2*6)+(1*9)=125
125 % 10 = 5
So 27068-69-5 is a valid CAS Registry Number.

27068-69-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,6-dimethyl-2-phenylpyridine

1.2 Other means of identification

Product number -
Other names 2-Phenyl-3,6-dimethylpyridin

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:27068-69-5 SDS

27068-69-5Relevant academic research and scientific papers

Chiral 1,2-dihydropyridine compound as well as preparation method and application thereof

-

Paragraph 0194-0196, (2020/01/03)

The invention discloses a synthesis method for preparing chiral polysubstituted 1,2-dihydropyridine as well as polysubstituted pyridine and chiral piperidine derived from chiral polysubstituted 1,2-dihydropyridine by using a "one-pot serial connection method". The method comprises the following step: by taking an imine compound and an aldehyde compound as raw materials, performing an asymmetric Mannich reaction, a Wittig reaction and an intramolecular ring-closing reaction in sequence, so as to synthesize a chiral 1,2-dihydropyridine compound with high three-dimensional selectivity. The product does not need to be purified, and a polysubstituted pyridine compound can be prepared through oxidation aromatization through further "one-pot serial connection", and a polysubstituted chiral piperidine compound can be also prepared through catalytic hydrogenation after separation and purification. The method starts from simple and easily obtained raw materials, separation and purification of anintermediate are avoided, and compounds of 1,2-dihydropyridine, polysubstituted pyridine and chiral piperidine are efficiently synthesized through simples steps of operation. Nitrogenous six-memberedring frameworks which are synthesized by using the method and disclosed by the invention are all common in many natural products and medicine molecules, and have great significances for acceleratingmedicine research and development.

NNN-Ruthenium Catalysts for the Synthesis of Pyridines, Quinolines, and Pyrroles by Acceptorless Dehydrogenative Condensation

Deng, Danfeng,Hu, Bowen,Yang, Min,Chen, Dafa

, p. 2386 - 2394 (2018/07/31)

The bidentate ruthenium complex (HO-C5H3N-CO-C5H3N-C5H4N)Ru(CO)2Cl2 (2) could transform to a tridentate product (HO-C5H3N-CO-C5H3N-C5H4N)Ru(CO)Cl2 (3), which further reacted with CH3ONa in the presence of PPh3 to convert to two complexes [(OC5H3N-CO-C5H3N-C5H4N)Ru(PPh3)2(CO)]Cl- (4) and [(OC5H3N-CO-C5H3N-C5H4N)Ru(PPh3)(CO)Cl] (5), via -OH deprotonation. The catalytic coupling cyclizations of secondary alcohols with amino alcohols were investigated, and complex 3 exhibited the highest activity. The coupling reactions proceeded in air with only 0.2 mol % catalyst loading and had a broad scope for the synthesis of pyridines, quinolones, and pyrroles.

Regioselective Pd-Catalyzed Synthesis of 2,3,6-Trisubstituted Pyridines from Isoxazolinones

Rieckhoff, Stefan,Hellmuth, Tina,Peters, René

, p. 6822 - 6830 (2015/10/05)

Substituted pyridines are prevalent heterocycles of fundamental importance. Their efficient regioselective preparation is often still a challenge despite a large number of reported synthetic methodologies. In this letter we report an operationally simple approach that makes use of readily accessible isoxazolinones. The protocol involves a Pd(II)-catalyzed C-regioselective 1,4-addition to vinylketones, followed by a Pd(0)-catalyzed transformation, which is assumed to proceed via vinylnitrene-Pd intermediates. Both hydrogen and air are necessary for the pyridine formation step and could be employed at ratios above the upper explosive limit thus avoiding a safety issue. This new strategy allows an effective, scalable and practical access to various previously unknown 2,3,6-trisubstituted pyridines.

Three-component coupling sequence for the regiospecific synthesis of substituted pyridines

Chen, Ming Z.,Micalizio, Glenn C.

, p. 1352 - 1356 (2012/03/11)

A de novo synthesis of substituted pyridines is described that proceeds through nucleophilic addition of a dithiane anion to an α,β- unsaturated carbonyl followed by metallacycle-mediated union of the resulting allylic alcohol with preformed trimethylsilane-imines (generated in situ by the low-temperature reaction of lithium hexamethyldisilazide with an aldehyde) and Ag(I)- or Hg(II)-mediated ring closure. The process is useful for the convergent assembly of di- through penta-substituted pyridines with complete regiochemical control.

Heteroaromatic synthesis via olefin cross-metathesis: Entry to polysubstituted pyridines

Donohoe, Timothy J.,Basutto, Jose A.,Bower, John F.,Rathi, Akshat

, p. 1036 - 1039 (2011/04/27)

The olefin cross-metathesis reaction provides a rapid and efficient method for the synthesis of α,β-unsaturated 1,5-dicarbonyl derivatives which then serve as effective precursors to mono-tetrasubstituted pyridines. Manipulation of the key 1,5-dicarbonyl intermediate allows access to pyridines with a wide range of substitution patterns. An extension of this methodology facilitates the preparation of pyridines embedded within macrocycles, as exemplified by an efficient synthesis of (R)-(+)-muscopyridine. High levels of regiocontrol, short reaction sequences, and facile substituent variation are all notable aspects of this methodology.(Figure Presented)

Intermolecular photoaddition reaction of benzenecarbothioamide with γ,δ-unsaturated ketones: A novel formation of cycloalkane-fused pyridine derivatives by photoinduced reaction

Oda, Kazuaki,Nakagami, Rikiji,Haneda, Michiko,Nishizono, Naozumi,Machida, Minoru

, p. 2019 - 2022 (2007/10/03)

Irradiation of benzenecarbothioamide with 2-(2-alkenyl)-cycloalkanone in benzene gives cycloalkane-fused pyridine derivatives in moderate yields.

α-PHENYLISOCINCHOMERONIC AND 4-AZAFLUORENONE 3-CARBOXYLIC ACIDS

Prostakov, N. S.,Sakha Shibu Rani,Mikhailova, N. M.,Sergeeva, N. D.

, p. 529 - 532 (2007/10/02)

3,6-Dimethyl-2-phenylpyridine, obtained on phenylation of 2,5-lutidine, has been used in the synthesis of α-phenylisocinchomeronic acid, derivatives of it, and also for the preparation of 4-azafluorenone 3-carboxylic acid.It was established that 4-hydroxy-3,6-dimethyl-2-phenylpyridine was formed on phenylation of 2,5-lutidine.

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