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2-(2-(4-bromophenoxy)ethoxy)ethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

333382-85-7

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333382-85-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 333382-85-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,3,3,8 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 333382-85:
(8*3)+(7*3)+(6*3)+(5*3)+(4*8)+(3*2)+(2*8)+(1*5)=137
137 % 10 = 7
So 333382-85-7 is a valid CAS Registry Number.

333382-85-7Relevant academic research and scientific papers

NEW HETEROCYCLIC COMPOUNDS

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Page/Page column 67; 110, (2019/06/17)

The invention provides new heterocyclic compounds having the general formula (IA) wherein A, L, X, Y, m, n, R1 and R2 are as described herein, compositions including the compounds, processes of manufacturing the compounds and methods of using the compounds.

Microwave mediated protection of hindered phenols and alcohols

Pothi, Tejas,Dawange, Mahesh,Chavan, Kamlesh,Sharma, Rajiv,Deka, Nabajyoti

, p. 706 - 711 (2013/03/28)

Hindered phenols and alcohols were protected as their corresponding ethers using different alkylating agents in presence of KOH/DMSO under microwave irradiation.

Synthesis of pyridinocrownophanes exhibiting high Ag+-affinity

Inokuma, Seiichi,Kimura, Koichi,Funaki, Takashi,Nishimura, Jun

, p. 123 - 130 (2007/10/03)

Crownophanes possessing a pyridine moiety were prepared by means of intramolecular [2 + 2] photocycloaddition of the styrene derivatives. The crown compounds having six to ten ethereal oxygens selectively extracted Ag+ with high efficiency in the liquid-liquid extraction. The high extractability and efficiency were maintained even at low pH region of the extraction system. From ESI-MS analysis, it was found that the crownophanes formed some kinds of complexes having 1:1 and 2:1 stoichiometry (host/guest) with Ag+ and Pb2+ in MeCN-H2O homogeneous system.

SELECTIV BROMINATION OF THE AROMATIC RING IN ω-PHENYLPOLYOXAALKANES AND ALKANOLS IN MICELLES

Jursic, Branko

, p. 1553 - 1558 (2007/10/02)

The regioselecticity of bromination of ω-phenylpolyoxaalkanes and alkanols by bromine in aqueous solution of dodecyl sulfate (SDS) and aqueous solution of cetyltrimethylammonium bromide (CTAB) are shown to be related to the average orientation of substrate as indicated by 1H NMR studies.Thus ortho-bromination is promoted at higher concentrations of the surfactant relative to pure water.In contrast, at an equal ratio of the surfactant and substrate para-bromination is promoted.The results are discussed with respect to the average orientation of substrate in a micellar microenvironment and the formation of an ether-bromine comples as possible bromination agent.

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