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1-Propanone, 2-bromo-1-(2-furanyl)-2-methyl- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20895-05-0

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20895-05-0 Usage

Classification

Organobromine compound

Structure

Ketone derivative with a 2-furanyl substituent on the alpha carbon and a bromine atom attached to the beta carbon

Uses

Reagent in organic synthesis, can undergo nucleophilic substitution and condensation reactions

Applications

Pharmaceutical and agrochemical industries for the synthesis of various compounds, potential uses in the development of new materials and chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 20895-05-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,8,9 and 5 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 20895-05:
(7*2)+(6*0)+(5*8)+(4*9)+(3*5)+(2*0)+(1*5)=110
110 % 10 = 0
So 20895-05-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H9BrO2/c1-8(2,9)7(10)6-4-3-5-11-6/h3-5H,1-2H3

20895-05-0Downstream Products

20895-05-0Relevant academic research and scientific papers

Intermolecular C-H Quaternary Alkylation of Aniline Derivatives Induced by Visible-Light Photoredox Catalysis

Cheng, Jie,Deng, Xia,Wang, Guoqiang,Li, Ying,Cheng, Xu,Li, Guigen

supporting information, p. 4538 - 4541 (2016/09/28)

The intermolecular direct C-H alkylation of aniline derivatives with α-bromo ketones to build a quaternary carbon center was reported with a visible-light catalysis procedure. The reaction covers a variety of functional groups with good to excellent yield

New Photocleavable Structures I: Synthesis of Hydroxyalkylphenone Analogues Electron-rich Heterocycles

Liska, Robert

, p. 1475 - 1486 (2007/10/03)

A series of photoinitiating compounds with the general structure ArCOCMe2OH, where Ar is 2-furyl (1a), 3-furyl (1b), 2-thienyl (2a), 3-thienyl (2b), 2-pyrrolyl (3a) and 3-pyrrolyl (3b), were prepared. The heterocyclic precursors were substituted by Friede

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