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Methanone, 3-benzofuranyl(4-methoxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

28222-80-2

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28222-80-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28222-80-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,2,2 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 28222-80:
(7*2)+(6*8)+(5*2)+(4*2)+(3*2)+(2*8)+(1*0)=102
102 % 10 = 2
So 28222-80-2 is a valid CAS Registry Number.

28222-80-2Relevant academic research and scientific papers

Synthesis, antimicrobial, and antioxidant activity of benzofuran barbitone and benzofuran thiobarbitone derivatives

Kenchappa,Bodke, Yadav D.,Asha,Telkar, Sandeep,Aruna Sindhe

, p. 3065 - 3081 (2014/05/06)

The synthesis of novel series of benzofuran derivatives, containing barbitone moiety, 5-[(2/4-substitutedphenyl)(5-substituted-1-benzofuran-2-yl) methylidene]pyrimidin-2,4,6(1H,3H,5H)-trione (4a-i) and thiobarbitone moiety, 5-[(2/4-substitutedphenyl)(5-su

Conformational Analysis of Organic Carbonyl Compounds. Part 5. p-Methoxybenzoyl Derivatives of Benzofuran, Benzothiophene, and Naphthalene

Benassi, Rois,Folli, Ugo,Iarossi, Dario,Schenetti, Luisa,Taddei, Ferdinando

, p. 351 - 358 (2007/10/02)

The conformational analysis of 2- and 3-(p-methoxybenzoyl)-benzofuran and -benzothiophene and 1- and 2-(p-methoxybenzoyl)naphthalene was performed by the n.m.r. lanthanide-induced shift (LIS) method on 1H and 13C chemical shifts with Yb(fod)3 as shi

Substituted benzofurans and benzothiophenes

-

, (2008/06/13)

The compounds are benzoyl benzofurans and benzothiophenes having pharmacological activity, in particular, coronary vasodilator activity useful for the treatment of angina pectoris and intermediates for the preparation thereof.

Pharmaceutical compositions and methods of producing coronary vasodilation

-

, (2008/06/13)

Pharmaceutical compositions and methods of producing coronary vasodilation by administering substituted benzofurans, for example 2-n-butyl-3-[4' -(2-hydroxy-3-isopropylamino)propoxybenzoyl] benzofuran.

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