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276690-15-4

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276690-15-4 Usage

Description

(2R,3R,5S)-3,5-DiMethyl-1-benzyloxy-2-hydroxy-8-(4-Methoxyphenoxy)-4-octanone is a complex organic compound characterized by its molecular structure and chemical properties. It is a colorless oil, indicating that it is a liquid at room temperature and has a relatively low molecular weight. (2R,3R,5S)-3,5-DiMethyl-1-benzyloxy-2-hydroxy-8-(4-Methoxyphenoxy)-4-octanone is an intermediate in the synthesis of Stigmatellin A (S686780), which is a natural product with potential biological activities.

Uses

1. Used in Pharmaceutical Industry:
(2R,3R,5S)-3,5-DiMethyl-1-benzyloxy-2-hydroxy-8-(4-Methoxyphenoxy)-4-octanone is used as an intermediate in the preparation of Stigmatellin A (S686780) for its potential pharmaceutical applications. Stigmatellin A is a natural product with various biological activities, and this compound plays a crucial role in its synthesis process.
2. Used in Chemical Research:
As a complex organic molecule, (2R,3R,5S)-3,5-DiMethyl-1-benzyloxy-2-hydroxy-8-(4-Methoxyphenoxy)-4-octanone can be used in chemical research for understanding its properties, reactivity, and potential applications in the synthesis of other related compounds. Its unique structure and properties make it an interesting subject for further study and development.

Check Digit Verification of cas no

The CAS Registry Mumber 276690-15-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,6,6,9 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 276690-15:
(8*2)+(7*7)+(6*6)+(5*6)+(4*9)+(3*0)+(2*1)+(1*5)=174
174 % 10 = 4
So 276690-15-4 is a valid CAS Registry Number.

276690-15-4Relevant articles and documents

Diastereo- and enantioselective total synthesis of stigmatellin A

Enders, Dieter,Geibel, Gunter,Osborne, Simon

, p. 1302 - 1309 (2007/10/03)

Stigmatellin A (1) isolated from the myxobacterium Stigmatella aurantiaca is a powerful inhibitor of electron transport in mitochondria and chloroplasts. The first highly diastereo- and enantioselective total synthesis of this important natural product is

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