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2-Hepten-1-ol, 7-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-6-[(4-methoxyphenyl)methoxy]-5-methyl, (2E,5R,6R)- is a complex organic compound with a molecular formula of C28H38O4Si. It is a chiral molecule, with the (2E,5R,6R) configuration indicating the specific arrangement of atoms in its structure. 2-Hepten-1-ol, 7-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-6-[(4-methoxyphenyl)methoxy]-5- methyl-, (2E,5R,6R)- features a 2-hepten-1-ol backbone, which is a seven-carbon chain with a hydroxyl group at the first carbon and a double bond between the second and third carbons. The molecule also contains a 1,1-dimethylethyldiphenylsilyl group attached to the seventh carbon, which provides steric bulk and may influence the compound's reactivity or physical properties. Additionally, it has a 4-methoxyphenylmethoxy group at the sixth carbon, contributing to its overall structure and potential applications. 2-Hepten-1-ol, 7-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-6-[(4-methoxyphenyl)methoxy]-5- methyl-, (2E,5R,6R)- is likely to be used in specialized chemical synthesis or as an intermediate in the production of pharmaceuticals or other complex organic molecules.

397886-59-8

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397886-59-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 397886-59-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,7,8,8 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 397886-59:
(8*3)+(7*9)+(6*7)+(5*8)+(4*8)+(3*6)+(2*5)+(1*9)=238
238 % 10 = 8
So 397886-59-8 is a valid CAS Registry Number.

397886-59-8Relevant academic research and scientific papers

Synthetic studies aimed at (-)-cochleamycin A. Evaluation of late-stage macrocyclization alternatives

Paquette, Leo A.,Chang, Jiyoung,Liu, Zuosheng

, p. 6441 - 6448 (2007/10/03)

An efficient route to the fully functionalized ABC ring systems of the unnatural enantiomer of cochleamycin A was developed. L-(-)-Malic and L-(-)-ascorbic acids served well as starting materials for the two building blocks used to construct an (E,Z,E)-1,

Studies aimed at the total synthesis of the antitumor antibiotic cochleamycin A. An enantioselective biosynthesis-based pathway to the AB bicyclic core

Chang, Jiyoung,Paquette, Leo A.

, p. 253 - 256 (2007/10/03)

Chemical equation presented A convergent, highly enantioselective synthesis of the fully functionalized AB sector of cochleamycin A is described. A pair of building blocks, crafted from L-malic and L-ascorbic acids, are conjoined in a manner that gives ri

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