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2-Methyl-1-[2,4,6-trihydroxy-3,5-bis(3-methyl-2-butenyl)phenyl]-1-propanone is a complex organic compound with the molecular formula C18H24O5. It is characterized by a propane-1-one backbone, with a methyl group at the 2-position and a substituted phenyl ring at the 1-position. The phenyl ring has three hydroxyl groups at the 2, 4, and 6 positions, and two 3-methyl-2-butenyl groups attached at the 3 and 5 positions. 2-Methyl-1-[2,4,6-trihydroxy-3,5-bis(3-methyl-2-butenyl)phenyl]-1-propanone is known for its unique structure and potential applications in various fields, such as pharmaceuticals and chemical research. Due to its complexity, it is often synthesized through multi-step processes and may exhibit specific chemical properties and reactivity patterns.

5880-42-2

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5880-42-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5880-42-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,8 and 0 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5880-42:
(6*5)+(5*8)+(4*8)+(3*0)+(2*4)+(1*2)=112
112 % 10 = 2
So 5880-42-2 is a valid CAS Registry Number.

5880-42-2Relevant academic research and scientific papers

PROCESSES FOR THE PREPARATION OF ORTHO-ALLYLATED HYDROXY ARYL COMPOUNDS

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Paragraph 00348; 00366, (2021/12/08)

The present application describes process for preparing an ortho-allylated hydroxy aryl compounds such as compounds of Formula (I) by reacting an allylic alcohol with a hydroxy aryl compound in the presence of aluminum compound selected from alumina and aluminum alkoxides and in a non-protic solvent wherein at least one carbon atom ortho to the hydroxy group in the hydroxy aryl compound is unsubstituted. The present application also includes compounds of Formula (I).

Expedient synthesis of ialibinones A and B by manganese(III)-mediated oxidative free radical cyclisation

Simpkins, Nigel S.,Weller, Michael D.

scheme or table, p. 4823 - 4826 (2010/10/02)

The tricyclic natural products ialibinone A and ialibinone B were prepared as a 41:59 mixture in four steps starting from phloroglucinol. The synthetic sequence involved (i) acylation of phloroglucinol under Friedel-Crafts conditions, (ii) double prenylat

Biomimetic synthesis of polycyclic polyprenylated acylphloroglucinol natural products isolated from hypericum papuanum

George, Jonathan H.,Hesse, Micha D.,Baldwin, Jack E.,Adlington, Robert M.

supporting information; experimental part, p. 3532 - 3535 (2010/09/18)

(Equation Presented). Biomimetic syntheses of three polycylic polyprenylated acylphloroglucinol natural products isolated from Hypericum papuanum, ialibinone A, ialibinone B, and hyperguinone B, have been accomplished by selective oxidative cyclizations o

A short biomimetic approach to the fully functionalized bicyclic framework of type A acylphloroglucinols

Couladouros, Elias A.,Dakanali, Marianna,Demadis, Konstantinos D.,Vidali, Veroniki P.

scheme or table, p. 4430 - 4433 (2009/12/24)

A biomimetic approach toward type A polyprenylated acylphlorogluclnols (PPAPs) Is described. The method Is based on a C-alkylation-cation cyclization reaction sequence, leading to a convenient buildup of molecular complexity, employing the simple and read

Polyhydroxyphenol derivatives and preventive and therapeutic agents for bone and cartilage diseases containing the same

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, (2008/06/13)

Compounds useful as preventive and therapeutic agents for bone and cartilage diseases; and drug compositions containing the same. The compounds are polyhydroxyphenol derivatives of general formula (I) and quinione analogues derived therefrom (wherein Rsu

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