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tert-butyl[(4-(2E-3,7-dimethyl-2,6-octadienyl)-3,5-bis(methoxymethoxy)benzyl)oxy]dimethylsilane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

252679-36-0

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  • tert-butyl[(4-(2E-3,7-dimethyl-2,6-octadienyl)-3,5-bis(methoxymethoxy)benzyl)oxy]dimethylsilane

    Cas No: 252679-36-0

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252679-36-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 252679-36-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,2,6,7 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 252679-36:
(8*2)+(7*5)+(6*2)+(5*6)+(4*7)+(3*9)+(2*3)+(1*6)=160
160 % 10 = 0
So 252679-36-0 is a valid CAS Registry Number.

252679-36-0Relevant articles and documents

Total synthesis and dual PPARα/γ agonist effects of Amorphastilbol and its synthetic derivatives

Kim, Taejung,Lee, Woojung,Jeong, Kyu Hyuk,Song, Jung Ho,Park, Soon-Hye,Choi, Pilju,Kim, Su-Nam,Lee, Seokjoon,Ham, Jungyeob

, p. 4122 - 4126 (2012/07/03)

Amorphastilbol (APH-1), isolated from a Robinia pseudoacacia var. umbraculifer seed extract, is a biologically interesting natural trans-stilbene compound with dual peroxisome proliferator-activated receptor (PPAR) α/γ agonist activity. After total synthesis of APH-1 and its derivatives by Pd-catalyzed Suzuki-Miyaura cross-coupling of a common (E)-styryl bromide intermediate and various aromatic trifluoroborate compounds, we biologically evaluated APH-2-APH-12 for PPAR agonist activity. APH-4 and APH-11 were effective PPARα/γ transcriptional activators, compared with APH-1. Therefore, we suggest that APH-4 and APH-11 are novel dual PPARα/γ agonists and are potentially useful for treating type 2 diabetes by enhancing glucose and lipid metabolism.

Total synthesis of pawhuskin C: A directed ortho metalation approach

Neighbors, Jeffrey D.,Salnikova, Maya S.,Wiemer, David F.

, p. 1321 - 1324 (2007/10/03)

The total synthesis of the opioid modulator pawhuskin C has been accomplished in eight steps from methyl 3,5-dihydroxybenzoate. The key step in this sequence is a directed ortho metalation reaction conducted without protection of a benzylic alcohol and th

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