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
20895-05-0Relevant articles and documents
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