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(2R,3R,4R)-1-(tert-Butyl-diphenyl-silanyloxy)-4-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-2-methyl-pentan-3-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

105676-41-3

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105676-41-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105676-41-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,6,7 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 105676-41:
(8*1)+(7*0)+(6*5)+(5*6)+(4*7)+(3*6)+(2*4)+(1*1)=123
123 % 10 = 3
So 105676-41-3 is a valid CAS Registry Number.

105676-41-3Relevant academic research and scientific papers

Aplyronine A, a potent antitumor macrolide of marine origin, and the congeners aplyronines B and C: isolation, structures, and bioactivities

Ojika, Makoto,Kigoshi, Hideo,Yoshida, Yoshifumi,Ishigaki, Takeshi,Nisiwaki, Masanori,Tsukada, Itaru,Arakawa, Masayuki,Ekimoto, Hisao,Yamada, Kiyoyuki

, p. 3138 - 3167 (2007/10/03)

Aplyronine A (2), a potent antitumor macrolide was isolated from the sea hare Aplysia kurodai together with the congeners aplyronines B (3) and C (4). The absolute stereostructure of aplyronine A (2) was determined by the instrumental analysis (mainly NMR and MS) and the enantioselective synthesis of the fragments obtained from chemical degradation of aplyronine A (2). The structures of aplyronines B (3) and C (4) were also elucidated. Cytotoxicity and antitumor activity of aplyronine A (2) were evaluated.

Studies on the Stereochemistry of Aplyronine A: Determination of the Stereochemistry of the C21-C34 Fragment

Ojika, Makoto,Kigoshi, Hideo,Ishigaki, Takeshi,Nisiwaki, Masanori,Tsukada, Itaru,et al.

, p. 8505 - 8508 (2007/10/02)

The absolute stereochemistry of the C21-C34 fragment 2 of aplyronine A (1), a potent antitumor substance of marine origin, was determined by the enantioselective synthesis.

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