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Benzeneoctanoic acid, 4-methoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24536-02-5

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24536-02-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24536-02-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,5,3 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 24536-02:
(7*2)+(6*4)+(5*5)+(4*3)+(3*6)+(2*0)+(1*2)=95
95 % 10 = 5
So 24536-02-5 is a valid CAS Registry Number.

24536-02-5Upstream product

24536-02-5Downstream Products

24536-02-5Relevant academic research and scientific papers

On the importance of the relative stereochemistry of substituents in the formation of nine-membered lactones by ring-closing metathesis

Cusson, Jean-Philippe,Chénard, Etienne,Hanessian, Stephen

, p. 1317 - 1324 (2015)

The effects of isopropyl substituents and molar concentration of diastereomeric esters toward the formation of nine-membered unsaturated lactones, in the context of the synthesis of the intermediates of the antihypertensive drug aliskiren, have been studied

Method of inhibiting parasitic activity

-

, (2008/06/13)

A method of inhibiting parasitic activity is disclosed in which the biosynthesis, structure and/or function of the glycosyl phosphatidylinositol (GPI) anchor of said parasite may be affected by incorporating into said GPI anchor selected analogs of myristic acid containing various heteroatoms, substituents and unsaturated bonds, including ester-containing analogs, ketocarbonyl-containing analogs, sulfur-containing analogs, double bond- and triple bond-containing analogs, aromatic moiety-containing analogs, nitrated analogs and halogenated analogs.

Dibenz[b,e]oxepinalkanoic acids as nonsteroidal antiinflammatory agents. 3. ω (6,11 Dihydro 11 oxodibenz[b,e]oxepin 2 yl)alkanoic acids

Aultz,McFadden,Lassman

, p. 1499 - 1501 (2007/10/13)

ω-(6,11-Dihydro-11-oxodibenz[b,e]oxepin-2-yl)butyric,-hexanoic, and -octanoic acids were evaluated in the carrageenan paw edema assay. The most active compound, the butyric acid analogue, was 1.80 times more potent than the hexanoic compound, 1.15 times m

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