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3-Hydroxy-2-methyl-1-phenyl-3-(pyridin-2-yl)propan-1-one is a complex organic compound with a molecular formula of C18H17NO2. It features a 3-hydroxyl group, a 2-methyl group, a 1-phenyl group, and a 3-(pyridin-2-yl) group attached to a propane-1-one backbone. 3-hydroxy-2-methyl-1-phenyl-3-(pyridin-2-yl)propan-1-one is characterized by its unique structure, which combines a ketone group with a pyridine ring and a phenyl ring, making it a potential candidate for various chemical and pharmaceutical applications. Its specific properties, such as solubility, reactivity, and potential uses, would depend on the context in which it is being considered, and further research would be needed to explore its full potential.

5325-67-7

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5325-67-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5325-67-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,2 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5325-67:
(6*5)+(5*3)+(4*2)+(3*5)+(2*6)+(1*7)=87
87 % 10 = 7
So 5325-67-7 is a valid CAS Registry Number.

5325-67-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-HYDROXY-2-METHYL-3-(2-PYRIDYL)-PROPIOPHENONE

1.2 Other means of identification

Product number -
Other names 3-hydroxy-2-methyl-1-phenyl-3-pyridin-2-yl-propan-1-one

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:5325-67-7 SDS

5325-67-7Downstream Products

5325-67-7Relevant academic research and scientific papers

Catalytic asymmetric aldol reactions in aqueous media using chiral bis-pyridino-18-crown-6 - Rare earth metal triflate complexes

Hamada, Tomoaki,Manabe, Kei,Ishikawa, Shunpei,Nagayama, Satoshi,Shiro, Motoo,Kobayashi, Sho

, p. 2989 - 2996 (2007/10/03)

Catalytic asymmetric aldol reactions in aqueous media have been developed using Pr(OTf)3 and chiral bis-pyrdino-18-crown-6 1. In the asymmetric aldol reaction using rare earth metal triflates (RE(OTf)3) and 1, slight changes in the i

Organic synthesis inside particles in water: Lewis acid-surfactant-combined catalysts for organic reactions in water using colloidal dispersions as reaction media

Manabe, Kei,Mori, Yuichiro,Wakabayashi, Takeshi,Nagayama, Satoshi,Kobayashi, Shu

, p. 7202 - 7207 (2007/10/03)

A Lewis acid - surfactant-combined catalyst (LASC) has been developed and applied to Lewis acid-catalyzed organic reactions in water. LASCs are composed of water-stable Lewis acidic cations such as scandium and anionic surfactants such as dodecyl sulfate

Lewis acid catalysis in aqueous media: Copper(II)-catalyzed aldol and allylation reactions in a water-ethanol-toluene solution

Kobayashi, Shu,Nagayama, Satoshi,Busujima, Tsuyoshi

, p. 959 - 960 (2007/10/03)

Cu(OTf)2 was found to be a stable Lewis acid in aqueous media and to activate carbonyl compounds effectively. Aldol reactions of silyl enol ethers with aldehydes and allylation reactions of tetraallyltin with carbonyl compounds proceeded smooth

Rare Earth Metal Complexes as Water-Tolerant Lewis Acid Catalysts in Organic Synthesis

Kobayashi,Hashiya,Ishitani,Moriwaki,Nagayama

, p. 193 - 202 (2007/10/03)

Rare earth metal triflates are stable in aqueous media and can act as Lewis acid catalysts in several carbon-carbon bond forming reactions. This article describes some of these reactions; aldol and Mannich-type reactions in aqueous solution, and Friedel-Crafts acylations and Fries rearrangement in organic solvents. The reactions proceeded smoothly in the presence of a catalytic amount of the triflate under mild conditions. Moreover, the catalysts could be recovered after the reactions were completed and could be reused.

Lanthanide Triflates as Water-Tolerant Lewis Acids. Activation of Commercial Formaldehyde Solution and Use in the Aldol Reaction of Silyl Enol Ethers with Aldehydes in Aqueous Media

Kobayashi, Shu,Hachiya, Iwao

, p. 3590 - 3596 (2007/10/02)

Lanthanide trifluoromethanesulfonates (triflates), especially ytterbium triflate (Yb(OTf)3), were found to be stable Lewis acids in water.In the presence of a catalytic amount of lanthanide triflate, formaldehyde in water solution (commercial formaldehyde

The aldol reaction of silyl enol ethers with aldehydes in aqueous media

Kobayashi,Hachiya

, p. 1625 - 1628 (2007/10/02)

The aldol reaction of silyl enol ethers with aldehydes is successfully carried out in aqueous media by using a lanthanide trifluoromethanesulfonate as a catalyst. Water soluble aldehydes are applicable and the catalyst can be recovered and reused in this

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