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1-phenyl-3-(pyridin-3-yl)propane-1,3-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

10472-95-4

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10472-95-4 Usage

Appearance

Yellow crystalline powder

Molecular weight

263.29 g/mol

Classification

Chalcone derivative, flavonoids

Usage

Synthesis of various pharmaceuticals

Biological activities

Antioxidant, anti-inflammatory, and anticancer properties

Therapeutic applications

Potential treatment of neurological disorders and metabolic diseases

Other potential uses

Fluorescent dye, chemical intermediate in organic synthesis

Check Digit Verification of cas no

The CAS Registry Mumber 10472-95-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,7 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10472-95:
(7*1)+(6*0)+(5*4)+(4*7)+(3*2)+(2*9)+(1*5)=84
84 % 10 = 4
So 10472-95-4 is a valid CAS Registry Number.

10472-95-4SDS

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 1-phenyl-3-pyridin-3-ylpropane-1,3-dione

1.2 Other means of identification

Product number -
Other names 1-phenyl-3-pyridin-3-yl-propane-1,3-dione

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:10472-95-4 SDS

10472-95-4Relevant academic research and scientific papers

Structure- and Temperature-Dependent Luminescence Properties of Threefold Interpenetrated Networks: Coordination Polymers Based on Dinuclear Gridlike Silver(I) Units

Zhan, Shun-Ze,Song, Huan-Quan,Guo, Liu-Jun,Sun, Raymond Wai-Yin,Li, Dan

, p. 5127 - 5133 (2017)

Dinuclear gridlike AgI structural units (1) based on (3-pyridyl)-5-R-pyrazole ligands are extended from oligomers (R = phenyl) to three threefold interpenetrated 3D coordination polymers (R = 3-pyridyl) with cds-a (augmented CdSO4) n

An effective preparation of both 1,3-diketones and nitriles from alkynones with oximes as hydroxide sources

Chen, Pei,Zhang, Qian-Qian,Guo, Jia,Chen, Lu-Lu,Wang, Yan-Bo,Zhang, Xiao

, p. 6958 - 6966 (2018/10/02)

An effective phosphine-catalyzed protocol has been established for the syntheses of 1,3-diketones and nitriles from alkynones with oximes as hydroxide surrogates. This method features the use of a phosphine catalyst, compatibility with various functional groups and ambient temperature, which makes this approach very practical. A plausible mechanism was proposed.

Variations in the blaise reaction: Conceptually new synthesis of 3-amino enones and 1,3-diketones

Rao, H. Surya Prakash,Muthanna, Nandurka

supporting information, p. 1525 - 1532 (2015/03/04)

Organic compounds with 3-amino enone or 1,3-diketone functional groups are extremely important, as they can be converted into a plethora of heterocyclic or carbocyclic compounds, or can be used as ligands in metal complexes. We have achieved a new, easy, straightforward and convenient synthesis of 3-amino enones and 1,3-diketones starting from aryl/heteroaryl/alkyl nitriles and 1-aryl/alkyl 2-bromoethanones. The reaction is a variation of the classical Blaise reaction, and it works with zinc and trimethylsilyl chloride as an activator. By running the hydrolysis of the reaction intermediate with HCl (3 N aq.) at 0-30 °C or at 100 °C, it is possible to form either 3-amino enones or 1,3-diketones, respectively. The newly developed method was used for the synthesis of avobenzone, an ingredient of sun-screen lotions. Furthermore, an easy synthesis of (Z)-3-amino-1-[4-(tertbutyl) phenyl]-3-(4-methoxyphenyl)prop-2-en-1-one, with UV/Vis absorption characteristics similar to those of avobenzone, was also achieved.

Synthesis, characterization and fluorescence properties of boron difluoride pyridyl-β-diketonate derivatives

Wang, Dun-Jia,Kang, Yan-Fang,Xu, Ben-Po,Zheng, Jing,Wei, Xian-Hong

supporting information, p. 419 - 422 (2013/03/14)

Five pyridyl-β-diketones were synthesized by Claisen condensation of ethyl nicotinate with various aryl methyl ketones in benzene in the presence of sodium amide as the base, and then reacted with boron trifluoride diethyl etherate in dichloromethane to a

RARE EARTH METAL COMPLEX

-

Paragraph 0078, (2013/12/03)

Provided is a rare earth metal complex including a rare earth metal atom and a β-diketone compound coordinated to the rare earth metal atom, the β-diketone compound being represented by the following Formula (1). In Formula (1), R represents a monovalent

Interaction of copper(II) with ditopic pyridyl-β-diketone ligands: Dimeric, framework, and metallogel structures

Dudek, Melanie,Clegg, Jack K.,Glasson, Christopher R. K.,Kelly, Norman,Glou, Kerstin,Gloe, Karsten,Kelling, Alexandra,Buschmann, Hans-Juergen,Jolliffe, Katrina A.,Lindoy, Leonard F.,Meehan, George V.

experimental part, p. 1697 - 1704 (2012/04/11)

The interaction of Cu(II) with three β-diketone ligands of type R 1C(O)CH2C(O)R2 (where R1 = 2-, 3-, or 4-pyridyl and R2 = C6H5, respectively), HL1-HL3, alo

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