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Butanal, 2-[(4-methoxyphenyl)methylene]-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75102-00-0

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75102-00-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75102-00-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,1,0 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 75102-00:
(7*7)+(6*5)+(5*1)+(4*0)+(3*2)+(2*0)+(1*0)=90
90 % 10 = 0
So 75102-00-0 is a valid CAS Registry Number.

75102-00-0Relevant academic research and scientific papers

Aromatic amides as potentiators of bioefficacy of anti-infective drugs

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Page/Page column 10, (2008/06/13)

The present invention relates to an aromatic substituted pentadienoic acid amides and there use in combination of specific amounts of aromatic amides i.e. 4-alkyl-5-(substituted phenyl)-2(E),4(E)-pentadienoic acid amides, its geometrical isomers or their dihydro or tetrahydro derivatives and an anti-infective drug useful in potentiating the bioefficacy of antiinfective drug. The combination of the present invention is useful in the treatment of certain infections and disease at lower concentration of anti-infectives necessary to inhibit the growth of microbial strains and may also find applications in reducing the resistance in microorganisms.

AROMATIC SUBSTITUTED PENTADIENOIC ACID AMIDE FOR COMBINATION WITH ANTI-INFECTIVE DRUGS

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Page/Page column 23, (2008/06/13)

The present invention relates to an aromatic substituted pentadienoic acid amides and there use in combination of specific amounts of aromatic amides i.e. 4-alkyl-5-(substituted phenyl)-2(E),4(E)-pentadienoic acid amides, its geometrical isomers or their dihydro or tetrahydro derivatives and an anti-infective drug useful in potentiating the bioefficacy of antiinfective drug. The combination of the present invention is useful in the treatment of certain infections and disease at lower concentration of anti-infectives necessary to inhibit the growth of microbial strains and may also find applications in reducing the resistance in microorganisms.

Synthesis of substituted hexa-3,5-dienoic acid methyl esters from conjugated dienones

Nongkhlaw,Nongrum,Myrboh

, p. 1300 - 1303 (2007/10/03)

Substituted hexa-3,5-dienoic acid methyl esters (2) were conveniently prepared in one step by 1,2-carbonyl transposition of the corresponding dienones (1) using lead(IV) acetate and boron trifluoride-diethyl ether in benzene at room temperature.

Nitro aliphatic compounds, process for preparation thereof and use thereof

-

, (2008/06/13)

New Nitro aliphatic compounds and their pharmaceutically acceptable salts are disclosed.

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