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ethyl 2-((2S,4S,6S)-6-(((2R,4R,6R)-6-(2-oxoheptadec-3-yn-1-yl)-2-phenyl-1,3-dioxan-4-yl)methyl)-2-phenyl-1,3-dioxan-4-yl)acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1443040-62-7

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1443040-62-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1443040-62-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,3,0,4 and 0 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1443040-62:
(9*1)+(8*4)+(7*4)+(6*3)+(5*0)+(4*4)+(3*0)+(2*6)+(1*2)=117
117 % 10 = 7
So 1443040-62-7 is a valid CAS Registry Number.

1443040-62-7Downstream Products

1443040-62-7Relevant articles and documents

Asymmetric Iterative Hydration of Polyene Strategy to Cryptocaryols A and B

Hunter, Thomas J.,Wang, Yanping,Zheng, Jiamin,O'Doherty, George A.

, p. 1700 - 1710 (2016/05/24)

The development of two iterative asymmetric hydration approaches to the synthesis of all syn- and syn/anti/syn-1,3,5,7-tetraol motifs is described. These pseudo-symmetric products are synthetic precursors for 1,3-hexol products. The utility of the route to the all syn-1,3,5,7-tetraol diastereoisomer was demonstrated with its use in the synthesis of cryptocaryols A and B, as well as, stereoisomers.

Cryptocaryol Structure-Activity Relationship Study of Cancer Cell Cytotoxicity and Ability to Stabilize PDCD4

Cuccarese, Michael F.,Wang, Yanping,Beuning, Penny J.,O'Doherty, George A.

, p. 522 - 526 (2014/06/09)

The synthetic cryptocaryols A and B and a series of their analogues have been evaluated for their cytotoxicity and their ability to stabilize the tumor suppressor PDCD4. Cytotoxicities in the 3 to 30 μM range were found. Both the cytotoxicity and PDCD4 stabilizing ability were tolerant of large stereochemical changes to the molecule. Co-dosing studies with cryptocaryols A and B and several known cancer drugs showed no measuable enhancement in cancer drug cytotoxicity.

Cryptocaryols A and B: Total syntheses, stereochemical revision, structure elucidation, and structure-activity relationship

Wang, Yanping,O'Doherty, George A.

, p. 9334 - 9337 (2013/07/25)

The first total syntheses and structural elucidation of cryptocaryol A and cryptocaryol B were achieved in 23 and 25 linear steps, respectively. The synthesis relied on the use of a key pseudo-Cs symmetric pentaol intermediate, which in a stere

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