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3-[4-benzyloxy-3-(4-methoxy-benzyloxy)-3,4,4a,6,9,9a-hexahydro-2H-1,5-dioxa-benzocyclohepten-2-yl]-1-(2,2-dimethyl-8,8a-dihydro-3aH-indeno[1,2-d]oxazol-3-yl)-2-(2-hydroxy-1-hydroxymethyl-but-3-enyloxy)-propan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

776315-70-9

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776315-70-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 776315-70-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,6,3,1 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 776315-70:
(8*7)+(7*7)+(6*6)+(5*3)+(4*1)+(3*5)+(2*7)+(1*0)=189
189 % 10 = 9
So 776315-70-9 is a valid CAS Registry Number.

776315-70-9Downstream Products

776315-70-9Relevant academic research and scientific papers

Stereocontrolled synthesis of the ABCDE ring moiety of ciguatoxin CTX3C

Kobayashi, Shoji,Takahashi, Yusuke,Komano, Kazuo,Alizadeh, Babak H.,Kawada, Yuuya,Oishi, Tohru,Tanaka, Shin-Ichiro,Ogasawara, Yoshihiro,Sasaki, Shin-Ya,Hirama, Masahiro

, p. 8375 - 8396 (2007/10/03)

The ABCDE ring moiety of ciguatoxin CTX3C, a major causative agent of ciguatera poisoning, was stereoselectively synthesized. The key transformations are a chiral auxiliary-based asymmetric alkylation and an asymmetric aldol condensation, which controlled

Highly stereocontrolled synthesis of the ABCD ring fragment of ciguatoxin CTX3C

Oishi,Tanaka,Ogasawara,Maeda,Oguri,Hirama

, p. 952 - 954 (2007/10/03)

A combination of asymmetric alkylation using (1R,2S)-1-amino-2-indanol derivative as a chiral auxiliary and the ring-closing metathesis reaction was shown to be an efficient method for synthesizing the ABCD ring fragment of ciguatoxin CTX3C.

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