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1-(2-hydroxy-4-methoxyphenyl)pentan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

372486-18-5

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372486-18-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 372486-18-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,2,4,8 and 6 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 372486-18:
(8*3)+(7*7)+(6*2)+(5*4)+(4*8)+(3*6)+(2*1)+(1*8)=165
165 % 10 = 5
So 372486-18-5 is a valid CAS Registry Number.

372486-18-5Relevant articles and documents

Platinum complexes with anti-tumor activity and production method of platinum complexes with anti-tumor activity

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Paragraph 0041; 0043; 0046-0047, (2020/01/03)

The invention discloses platinum complexes with anti-tumor activity, and relates to the technical field of platinum complexes. The platinum complexes with anti-tumor activity comprise a complex A anda complex B, wherein with resorcinol as an initial raw m

Application of paeonol derivatives with vasodilator activity

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Paragraph 0028; 0035-0037, (2018/12/13)

The invention provides application of paeonol derivatives with vasodilator activity. The method comprises the following steps: carrying out a methylation reaction of 2,4-dihydroxyphenylpentanone underalkaline conditions, sequentially extracting and drying

Primulin derivative as well as synthesis method and application of primulin derivative

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Paragraph 0015, (2018/01/11)

The invention discloses a primulin derivative with antibacterial activity shown as the structural general formula (I), wherein R is selected from C2-C20 alkyls. The primulin derivative is prepared from raw materials including m-dihydroxybenzene and a fatty acid derivative by the steps: carrying out Friedel-Crafts acylation and methylation to synthesize a paeonol derivative, and carrying out oxidization after carrying out carbonyl reduction. The primulin derivative has good antibacterial activity and can be used as a potential antibacterial agent.

Synthesis and lipase-mediated stereoselective deacetylation of (±)-3-acetoxymethyl-3-alkyl-7-methoxychroman-4-ones

Poonam,Prasad, Ashok K,Azim, Abul,Kumar, Rajesh,Jain, Subhash C,Parmar, Virinder S,Olsen, Carl E,Errington, William

, p. 7395 - 7402 (2007/10/03)

Six (±)-3-acetoxymethyl-3-alkyl-7-methoxychroman-4-ones have been synthesized in four steps starting with the coupling of resorcinol with corresponding aliphatic acid leading to the formation of 2,4-dihydroxyphenyl alkyl ketones, which upon monomethylation and hydroxymethylation, followed by acetylation afforded the racemic acetoxymethylated compounds in 17-30% overall yields. Candida rugosa lipase-catalyzed deacetylation of (±)-3-acetoxymethylchromanones in diisopropyl ether exhibited fairly moderate enantioselectivity.

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