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(E)-(2S,6R,8S)-8-((S)-2-{(R)-2-[((S)-2-tert-Butoxycarbonylamino-propionyl)-methyl-amino]-3-[4-(tert-butyl-dimethyl-silanyloxy)-3-iodo-phenyl]-propionylamino}-propionyloxy)-2,4,6-trimethyl-non-4-enoic acid 4-methoxy-benzyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

156706-65-9

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156706-65-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 156706-65-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,7,0 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 156706-65:
(8*1)+(7*5)+(6*6)+(5*7)+(4*0)+(3*6)+(2*6)+(1*5)=149
149 % 10 = 9
So 156706-65-9 is a valid CAS Registry Number.

156706-65-9Relevant academic research and scientific papers

An expeditious synthesis of geodiamolide a, an 18-membered cytotoxic depsipeptide from marine sponges

Shioiri, Takayuki,Imaed, Takayuki,Hamad, Yasumasa

, p. 421 - 442 (2007/10/03)

Geodiamolide A (1) has been efficiently synthesized from the polypropionate and tripeptide units using the Evans asymmetric alkylation, the Mitsunobu esterification, and the macrolactamization with diphenyl phosphorazidate (DPPA) as key steps. Efficient esterification between the complex polyketide and tripeptide units was also realized under high pressure conditions.

Efficient syntheses of geodiamolide A and jaspamide, cytotoxic and antifungal cyclic depsipeptides of marine sponge origin

Imaeda, Takayuki,Hamada, Yasumasa,Shioiri, Takayuki

, p. 591 - 594 (2007/10/02)

Geodiamolide A (1a) and jaspamide (2) have been efficiently synthesized by use of the Evans asymmetric alkylation, the Mitsunobu esterification, and the DPPA macrolactamization as key steps.

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