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(E)-2-(3,7-dimethylocta-2,6-dien-1-yl)-1,5-dimethoxy-3-methylbenzene is a complex organic compound with a molecular formula of C19H26O2. It is characterized by a benzene ring with a methyl group at the 3-position, two methoxy groups at the 1 and 5 positions, and a 3,7-dimethylocta-2,6-dien-1-yl group attached to the 2-position. (E)-2-(3,7-dimethylocta-2,6-dien-1-yl)-1,5-dimethoxy-3-methylbenzene is known for its aromatic properties and is often found in the essential oils of plants, particularly in the family Lamiaceae. It is used in the fragrance industry for its pleasant scent and can also be found in some natural products, such as certain types of basil. The compound's structure and properties make it a valuable component in the synthesis of various pharmaceuticals and agrochemicals.

83036-48-0

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83036-48-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83036-48-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,0,3 and 6 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 83036-48:
(7*8)+(6*3)+(5*0)+(4*3)+(3*6)+(2*4)+(1*8)=120
120 % 10 = 0
So 83036-48-0 is a valid CAS Registry Number.

83036-48-0Downstream Products

83036-48-0Relevant academic research and scientific papers

Synthesis of natural product-like polyprenylated phenols and quinones: Evaluation of their neuroprotective activities

Kamauchi, Hitoshi,Oda, Takumi,Horiuchi, Kanayo,Takao, Koichi,Sugita, Yoshiaki

, (2019/11/26)

Twenty-seven natural product-like polyprenylated phenols and quinones were synthesized and their neuroprotective activity was tested using human monoamine oxidase B (MAO-B) and SH-SY5Y cells. Eight compounds inhibited MAO-B (IC50 values 25 μM

Antiproliferative effect and apoptotic activity of linear geranylphenol derivatives from phloroglucinol and orcinol

Taborga, Lautaro,Espinoza, Luis,Moller, Alejandra,Carrasco, Héctor,Cuellar, Mauricio,Villena, Joan

, p. 22 - 29 (2016/02/12)

Sixteen synthetic linear derivatives geranylphenols, were obtained from phloroglucinol and orcinol, and cytotoxic activity was evaluated in vitro against cancer cell lines (HT-29, PC-3, MDA-MB231, DU-145) and one non-tumor cell line, human dermal fibrobla

AN EFFICIENT REGIO- AND STEREOSPECIFIC ALKENYLATION OF PHENOLIC ETHERS BY PRENYL AND GERANYL DIISOPROPYL PHOSPHATES

Araki, Shuki,Manabe, Shin-ichi,Butsugan, Yasuo

, p. 797 - 800 (2007/10/02)

Prenyl and geranyl diisopropyl phosphates readily alkenylate a variety of phenolic ethers regio- and stereospecifically without any appreciable side reactions.

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