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tert-Butyl-dimethyl-((2R,4aR,6S,7R,8aS)-2-phenyl-6-vinyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yloxy)-silane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

436153-69-4

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436153-69-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 436153-69-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,6,1,5 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 436153-69:
(8*4)+(7*3)+(6*6)+(5*1)+(4*5)+(3*3)+(2*6)+(1*9)=144
144 % 10 = 4
So 436153-69-4 is a valid CAS Registry Number.

436153-69-4Downstream Products

436153-69-4Relevant academic research and scientific papers

Studies toward the total synthesis of gymnocin A, a cytotoxic polyether: A highly convergent entry to the F-N ring fragment

Sasaki, Makoto,Tsukano, Chihiro,Tachibana, Kazuo

, p. 1747 - 1750 (2002)

Matrix presented An efficient and highly convergent synthesis of the FGHIJKLMN ring fragment of gymnocin A, a cyctotoxic polycyclic ether isolated from the notorious red-tide forming dinoflagellate Gymnodinium mikimotoi, has been achieved. The present syn

Studies toward brevisulcenal F via convergent strategies for marine ladder polyether synthesis

Katcher, Matthew H.,Jamison, Timothy F.

supporting information, p. 1111 - 1122 (2018/02/09)

Shortly after the initial isolation of marine ladder polyether natural products, biomimetic epoxide-opening cascade reactions were proposed as an efficient strategy for the synthesis of these compounds. However, difficulties in assembling the cascade precursors have limited the realization of these cascades. In this report, we describe strategies that provide convergent access to cascade precursors via regioselective allylation and efficient fragment coupling. We then investigate epoxide-opening cascades promoted by strong bases for the formation of fused tetrahydropyrans. These strategies are evaluated in the context of the synthesis of rings CDEFG of brevisulcenal F.

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