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2-((E)-3,7-Dimethyl-octa-2,6-dienyl)-1,3-dimethoxy-5-propyl-benzene is a complex organic compound with a molecular formula of C19H30O2. It is characterized by a benzene ring with a 3,7-dimethyl-octa-2,6-dienyl group attached at the 2-position, and two methoxy groups at the 1 and 3 positions. Additionally, a propyl group is attached at the 5 position. This chemical structure suggests that it may have potential applications in the synthesis of fragrances, pharmaceuticals, or other specialty chemicals due to its unique arrangement of functional groups. The compound's specific properties, such as solubility, stability, and reactivity, would depend on the context in which it is used and would require further investigation for specific applications.

83036-51-5

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83036-51-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83036-51-5 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, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 83036-51:
(7*8)+(6*3)+(5*0)+(4*3)+(3*6)+(2*5)+(1*1)=115
115 % 10 = 5
So 83036-51-5 is a valid CAS Registry Number.

83036-51-5Downstream Products

83036-51-5Relevant academic research and scientific papers

CATALYTIC CANNABIGEROL PROCESSES AND PRECURSORS

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Paragraph 0111; 0121, (2021/10/11)

The present disclosure relates to cannabigerol sulfonate esters and processes for their use to prepare cannabigerol (CBG) and related compounds, including cannabigerobutol (CBGB), cannabigerovarin (CBGV), and cannabigerophorbol (CBGP). In a preferred embodiment, the cannabigerol sulfonate ester is (E)-4-(3, 7-5 dimethylocta-2,6-dienyl)-3,5-bis(trimetbylsilyloxy)phenyl trifluoromethanesulfonate. In a preferred process, the trifluoromethansulfonate leaving group is replaced by an alkyl group. The disclosure also relates to the use of catalysts and catalytic processes for the preparation of cannabigerol and related compounds from the cannabigerol sulfonate esters.

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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