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3-acetyl-1-benzyl-2-hydroxy-6-methylpyridin-4(1H)-one is a complex organic compound with the molecular formula C16H15NO3. It features a pyridin-4(1H)-one core structure, which is a heterocyclic compound with a nitrogen atom in the ring. The molecule has a 3-acetyl group, indicating the presence of an acetate group attached to the third carbon of the pyridine ring. Additionally, it has a benzyl group attached to the first carbon, which is a phenylmethyl group, and a hydroxyl group at the second carbon. The 6-methyl group signifies a methyl group attached to the sixth carbon of the pyridine ring. 3-acetyl-1-benzyl-2-hydroxy-6-methylpyridin-4(1H)-one is known for its potential applications in pharmaceuticals and as a synthetic intermediate in the preparation of various biologically active molecules. Its chemical structure and functional groups contribute to its reactivity and potential interactions with biological targets, making it a compound of interest in the field of medicinal chemistry.

26162-40-3

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26162-40-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26162-40-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,1,6 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 26162-40:
(7*2)+(6*6)+(5*1)+(4*6)+(3*2)+(2*4)+(1*0)=93
93 % 10 = 3
So 26162-40-3 is a valid CAS Registry Number.

26162-40-3SDS

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 3-acetyl-1-benzyl-4-hydroxy-6-methylpyridin-2-one

1.2 Other means of identification

Product number -
Other names 3-acetyl-1-benzyl-4-hydroxy-6-methyl-1H-pyridin-2-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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:26162-40-3 SDS

26162-40-3Relevant academic research and scientific papers

Metal catalysed reactions of β,β′-tricarbonyl derivatives with isocyanates

Veronese, Augusto C.,Durini, Elisa,Bertolasi, Valerio,Basato, Marino,Tubaro, Cristina

experimental part, p. 8313 - 8316 (2010/11/17)

The reactions of β,β′-tricarbonyl derivatives with isocyanates are catalysed by 2 mol % transition metal acetylacetonates (e.g., [Co(acac)2] and [Zn(acac)2]) at room temperature. 3-Oxo-1,5-pentanedioic acid dimethylester (1) reacts with RNCO (R=Et, CH 2CHCH2, CH2Ph, Ph, 4-Cl-Ph) to give 1:1 adducts involving the formation of a new C-C bond between the intercarbonylic methylene and the isocyanato group. Under similar conditions 2,4,6-heptanetrione (2) reacts with the same isocyanates to afford pyridinone and pyranone derivatives resulting from the cyclisation of unstable 1:1 and 1:2 adducts.

Cycloadditions in Syntheses. Part 28. 2-Azabicyclohexane-3,5-dione and its Derivatives: Synthesis and Transformation to Azetidin-2-ones

Katagiri, Nobuya,Sato, Masayuki,Yoneda, Naoki,Saikawa, Satoshi,Sakamoto, Toshiyuki,et al.

, p. 1289 - 1296 (2007/10/02)

2-Azabicyclohexane-3,5-dione has been synthesized via photopyridone formation from 4-(dimethyl-t-butylsiloxy)- or 4-alkoxy-2-pyridones followed by mild acid hydrolysis.The title compound and its derivatives react with a variety of nucleophiles (ROH

REACTION OF ETHYL β-ALKYLAMINOCROTONATES IN THE PRESENCE OF ORGANIC ACID

Yamato, Masatoshi,Sato, Koichi,Hashigaki, Kuniko,Ninomiya, Mayumi

, p. 1263 - 1268 (2007/10/02)

Condensation of ethyl β-alkylaminocrotonates, obtained from ethyl acetoacetate and amines, in the presence of 3-mercaptopropionic acid gave 1,6-naphthyridine-2,5-dione derivatives.The structures of these compounds were determined on the basis of several i

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