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(2S,4aR,6S,7R,9S,10aS)-7-Benzyloxy-2-[(1S,2S)-2-benzyloxy-2-((5R,7S,8R,9S,10S)-8-methoxymethoxy-9,10-dimethyl-1,6-dioxa-spiro[4.5]dec-7-yl)-1-methyl-ethyl]-6-benzyloxymethyl-9-methyl-octahydro-1,5-dioxa-benzocycloocten-3-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

253172-22-4

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253172-22-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 253172-22-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,3,1,7 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 253172-22:
(8*2)+(7*5)+(6*3)+(5*1)+(4*7)+(3*2)+(2*2)+(1*2)=114
114 % 10 = 4
So 253172-22-4 is a valid CAS Registry Number.

253172-22-4Upstream product

253172-22-4Relevant academic research and scientific papers

Convergent synthesis of the HIJKLM ring fragment of ciguatoxin CTX3C

Uehara, Hisatoshi,Oishi, Tohru,Inoue, Masayuki,Shoji, Mitsuru,Nagumo, Yoko,Kosaka, Masashi,Le Brazidec, Jean-Yves,Hirama, Masahiro

, p. 6493 - 6512 (2007/10/03)

Ciguatoxin CTX3C is a representative congener of the ciguatoxins, which are known to be the principal causative agents of ciguatera food poisoning. The structure of CTX3C spans more than 3nm and is characterized by 13 ether rings. To attain a practical construction of this molecule, efficient supplies of the structural fragments are crucial. Herein we report the convergent synthesis of the HIJKLM ring fragment and present a new carbonyl olefination protocol to cyclize the J ring using low-valent titanium.

Convergent synthesis of the IJKLM ring fragment of ciguatoxin CTX3C

Oishi, Tohru,Nagumo, Yoko,Shoji, Mitsuru,Le Brazidec, Jean-Yves,Uehara, Hisatoshi,Hirama, Masahiro

, p. 2035 - 2036 (2007/10/03)

The IJKLM ring fragment of CTX3C, an important member of the ciguatoxin family, was synthesized via ring-closing metathesis using the Tebbe reagent and an improved method of reductive hydroxy ketone cyclization.

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