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4-benzyloxy-17-methoxy-2-oxatricyclo[13.2.2.13,7]eicosa-1(18),3(20),4,6,15(19),16-hexaen-10-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

936253-56-4

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936253-56-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 936253-56-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,6,2,5 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 936253-56:
(8*9)+(7*3)+(6*6)+(5*2)+(4*5)+(3*3)+(2*5)+(1*6)=184
184 % 10 = 4
So 936253-56-4 is a valid CAS Registry Number.

936253-56-4Downstream Products

936253-56-4Relevant academic research and scientific papers

First total synthesis of cytotoxic diarylheptanoids, galeon, and pterocarine

Wang, Qian,Son, Jong-Keun,Jahng, Yurngdong

, p. 675 - 681 (2007/10/03)

The first total synthesis of cytotoxic diphenyl ether-type diarylheptanoids, galeon and pterocarine, was described in which the Ullmann reaction was employed at the final step for the diaryl ether formation of key intermediate, 1-(3-bromo-4-benzyloxypheny

A versatile synthesis of cyclic diphenyl ether-type diarylheptanoids: Acerogenins, (±)-galeon, and (±)-pterocarine

Jeong, Byeong-Seon,Wang, Qian,Son, Jong-Keun,Jahng, Yurngdong

, p. 1338 - 1344 (2008/09/18)

A versatile method for the total synthesis of cyclic diphenyl ether-type diarylheptanoids, acerogenin C, acerogenin L, (±)-galeon, and (±)-pterocarine was described. The Ullmann reaction of suitably substituted linear diphenylheptanoids was employed for t

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