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1-(4-(2-methylallyloxy)phenyl)ethanone is an organic compound with the molecular formula C12H14O2. It is a derivative of acetophenone, featuring a phenyl group attached to a methyl group and a 2-methylallyloxy group. 1-(4-(2-methylallyloxy)phenyl)ethanone is characterized by its aromatic structure and the presence of a carbonyl group, which contributes to its reactivity and potential applications in chemical synthesis. It is a colorless to pale yellow liquid with a distinct aroma, and it is used in the synthesis of various pharmaceuticals, fragrances, and other organic compounds. Due to its specific functional groups, it can participate in a range of chemical reactions, such as nucleophilic addition, oxidation, and reduction, making it a versatile building block in organic chemistry.

2086-08-0

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2086-08-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2086-08-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,8 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2086-08:
(6*2)+(5*0)+(4*8)+(3*6)+(2*0)+(1*8)=70
70 % 10 = 0
So 2086-08-0 is a valid CAS Registry Number.

2086-08-0Relevant academic research and scientific papers

Palladium-Catalyzed Tandem Oxidative Arylation/Olefination of Aromatic Tethered Alkenes/Alkynes

Gao, Yang,Gao, Yinglan,Wu, Wanqing,Jiang, Huanfeng,Yang, Xiaobo,Liu, Wenbo,Li, Chao-Jun

, p. 793 - 797 (2017)

We describe herein a palladium-catalyzed tandem oxidative arylation/olefination reaction of aromatic tethered alkenes/alkynes for the synthesis of dihydrobenzofurans and 2 H-chromene derivatives. This reaction features a 1,2-difunctionalization of C?C π-bond with two C?H bonds using O2as terminal oxidant at room temperature. The products obtained are valuable synthons and important scaffolds in biological agents and natural products.

Pd-Catalyzed regioselective hydroesterification of 2-allylphenols to seven-membered lactones without external CO gas

Chang, Wenju,Li, Jingfu,Ren, Wenlong,Shi, Yian

supporting information, p. 3047 - 3052 (2016/03/19)

Effective Pd-catalyzed regioselective hydroesterification of 2-allylphenols with phenyl formate is described. A variety of seven-membered lactones can be obtained in good yields under mild conditions without the use of toxic CO gas.

CARBINOL DERIVATIVES HAVING CYCLIC LINKER

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Page/Page column 78-79, (2010/03/31)

[Object] To provide a novel LXRβ agonist that is useful as a preventative and/or therapeutic agent for atherosclerosis; arteriosclerosis such as those resulting from diabetes; dyslipidemia; hypercholesterolemia; lipid-related diseases; inflammatory diseases that are caused by inflammatory cytokines; skin diseases such as allergic skin diseases; diabetes; or Alzheimer's disease. [Solving Means] A carbinol compound represented by the following general formula (I) or salt thereof, or their solvate.

CARBINOL DERIVATIVES HAVING HETEROCYCLIC LINKER

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Page/Page column 33, (2010/12/29)

[Object] It is to provide a novel LXRβ agonist useful as a preventative and/or therapeutic agent for atherosclerosis; arteriosclerosis such as those resulting from diabetes; dyslipidemia; hypercholesterolemia; lipid-related diseases; inflammatory diseases that are caused by inflammatory cytokines; skin diseases such as allergic skin diseases; diabetes; or Alzheimer's disease. [Solving Means] A carbinol compound represented by the following general formula (I) or salt thereof, or their solvate: (wherein, each V and W independently show N or C—R7; each X and Y independently show CH2, C═O, SO2, etc; Z shows CH or N; each R1, R2 and R7 independently show a hydrogen atom, C1-8 alkyl group, etc.; R3 shows C1-8 alkyl group; R4 shows an optionally substituted C6-10 aryl group or an optionally substituted 5- to 11-membered heterocyclic group; R5 and R6 show a hydrogen atom, etc.; L shows a C1-8 alkyl chain optionally substituted with an oxo group, etc.; and n shows any integer of 0 to 2.)

Pd-Catalyzed intramolecular oxyalkynylation of alkenes with hypervalent iodine

Nicolal, Stefano,Erard, Stephane,Gonzalez, Davinla Fernandez,Waser, Jerome

supporting information; experimental part, p. 384 - 387 (2010/03/04)

(Figure presented) The first example of intramolecular oxyalkynylation of nonactivated alkenes using oxidative Pd chemistry is reported. Both phenol and aromatic or aliphatic acid derivatives could be used under operator-friendly conditions (room temperature, technical solvents, under air). The discovery of the superiority of benzlodoxolone-derlved hypervalent iodine reagent 3d as an alkyne transfer reagent further expands the rapidly increasing utility of hypervalent iodine reagents in catalysis and is expected to have important implications for other similar processes.

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