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Benzene, 1,2,3,4-tetramethoxy-5-methyl-6-(3,7,11-trimethyl-2,6,10-dodecatrienyl) -, (E,E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

95778-33-9

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95778-33-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95778-33-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,7,7 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 95778-33:
(7*9)+(6*5)+(5*7)+(4*7)+(3*8)+(2*3)+(1*3)=189
189 % 10 = 9
So 95778-33-9 is a valid CAS Registry Number.

95778-33-9Relevant 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

A convergent approach to coenzyme Q

Lipshutz, Bruce H.,Bulow, Gerd,Fernandez-Lazaro, Fernando,Kim, Sung-Kyu,Lowe, Richard,Mollard, Paul,Stevens, Kirk L.

, p. 11664 - 11673 (2007/10/03)

Syntheses of coenzyme Q3-8 are described, as well as related systems such as plastoquinone-5. Preparation of the higher homologues of the ubiquinones relies on two new conjunctive reagents, or "linchpins", each of which ultimately corresponds to two or three prenyl units. These allow for attachment of a polyprenyl halide at one end, followed by a Ni(0)-catalyzed cross-coupling at the other terminus with a chloromethylated p-quinone.

Total Synthesis of Linear Polyprenoids. 2. Improved preparation of the Aromatic Nucleus of Ubiquinone

Keinan, Ehud,Eren, Doron

, p. 3872 - 3875 (2007/10/02)

Highly efficient copper-catalyzed polymethoxylation of tribromocresol is the key process in a three-step, practical approach to obtain ubiquinone 0 from p-cresol.Short syntheses of several ubiquinones were achieved via direct, copper-mediated coupling of 2-lithio-3,4,5,6-tetramethoxytoluene to the appropriate polyprenyl bromide.

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