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5-dodecyl-3-(phenylmethyl)isoxazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

159458-29-4

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159458-29-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 159458-29-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,4,5 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 159458-29:
(8*1)+(7*5)+(6*9)+(5*4)+(4*5)+(3*8)+(2*2)+(1*9)=174
174 % 10 = 4
So 159458-29-4 is a valid CAS Registry Number.

159458-29-4Relevant academic research and scientific papers

Heterocyclic-substituted alkylamide acat inhibitors

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Example 128, (2010/11/29)

Pharmaceutically useful compounds having ACAT inhibitory activity of the formula wherein n is 0, 1, or 2, for X other than tetrazole and n = 2 then R2 = R3 = H; R1 is phenyl, substituted phenyl, naphthyl, substituted naphthyl, a heteroaromatic group or a hydrocarbon group having from one to 18 carbon atoms; R2 and R3 are hydrogen, halo, hydroxy, alkyl, alkenyl, cycloalkyl, phenyl, substituted phenyl, a heteroaryl, or form a spiroalkyl group; x is a 5-membered heteromonocyclic group containing at least one to four heteroatoms selected from the group consisting of isothiazole, oxazole, thiazole, imidazole, furan, thiophene, pyrrole, tetrazole, 1,2,3-triazole, 1,2,4-oxadiazole, 1,3,4-oxadiazole, 1,3,4-thiadiazole, 1,2,4-triazole, and 1,2,4-oxadiazole said heteromonocyclic group being unsubstituted or substituted at any available position along the ring,

Heterocyclic amides: Inhibitors of acyl-CoA:cholesterol O-acyl transferase with hypocholesterolemic activity in several species and antiatherosclerotic activity in the rabbit

White, Andrew D.,Purchase II, Claude F.,Picard, Joseph A.,Anderson, Maureen K.,Mueller, Sandra Bak,Bocan, Thomas M. A.,Bousley, Richard F.,Hamelehle, Katherine L.,Krause, Brian R.,Lee, Peter,Stanfield, Richard L.,Reindel, James F.

, p. 3908 - 3919 (2007/10/03)

A series of heterocyclic amides were synthesized and evaluated as inhibitors of acyl-CoA: cholesterol O-acyltransferase (ACAT) in vitro and for cholesterol lowering in cholesterol-fed rats. Compounds were evaluated for cell-based macrophage ACAT inhibitio

Isoxazolyl-substituted alkyl amide ACAT inhibitors

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, (2008/06/13)

Pharmaceutically useful compounds having ACAT inhibitory activity of the formula STR1 wherein n is 0, 1, or 2, for X other than tetrazole and n=2 then R2 =R3 =H; R1 is phenyl, substituted phenyl, naphthyl, substituted naphthyl, a heteroaromatic group or a hydrocarbon group having from one to 18 carbon atoms; R2 and R3 are hydrogen, halo, hydroxy, alkyl, alkenyl, cycloalkyl, phenyl, substituted phenyl, a heteroaryl, or form a spiroalkyl group; X is a heteromonocyclic 5-membered ring containing one to four heteroatoms, said heteroatoms being nitrogen, oxygen or sulfur, and combination thereof; and R4 is a hydrocarbon group having from one to 20 carbon atoms are described as well as methods of their manufacture.

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