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(2R,3S,4R,5R,6S)-2-((S)-1-Benzyloxymethoxy-ethyl)-6-hydroxymethyl-3,5-dimethyl-tetrahydro-pyran-4-ol is a complex organic molecule with a tetrahydro-pyran-4-ol core structure. It features a benzyl group, a hydroxymethyl group, and a dimethyl substituent, along with an ether linkage and an ethyl group. The presence of multiple chiral centers results in a mixture of stereoisomers, which contribute to its complex and unique properties.

104206-08-8

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104206-08-8 Usage

Uses

Used in Pharmaceutical Industry:
(2R,3S,4R,5R,6S)-2-((S)-1-Benzyloxymethoxy-ethyl)-6-hydroxymethyl-3,5-dimethyl-tetrahydro-pyran-4-ol is used as a pharmaceutical compound for its potential therapeutic applications. Its versatile structure and functional groups allow for the development of new drugs targeting various diseases and conditions.
Used in Natural Products Industry:
In the natural products industry, (2R,3S,4R,5R,6S)-2-((S)-1-Benzyloxymethoxy-ethyl)-6-hydroxymethyl-3,5-dimethyl-tetrahydro-pyran-4-ol is used as a key component in the synthesis of natural product derivatives. Its unique properties and functional groups enable the creation of novel compounds with potential biological activities.
Used in Organic Synthesis:
(2R,3S,4R,5R,6S)-2-((S)-1-Benzyloxymethoxy-ethyl)-6-hydroxymethyl-3,5-dimethyl-tetrahydro-pyran-4-ol is utilized as a building block in organic synthesis. Its complex structure and multiple functional groups make it a valuable intermediate for the synthesis of a wide range of organic compounds, including pharmaceuticals, agrochemicals, and specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 104206-08-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,2,0 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 104206-08:
(8*1)+(7*0)+(6*4)+(5*2)+(4*0)+(3*6)+(2*0)+(1*8)=68
68 % 10 = 8
So 104206-08-8 is a valid CAS Registry Number.

104206-08-8Relevant academic research and scientific papers

THE ESTER ENOLATE CLAISEN REARRANGEMENT. SYNTHESIS OF A C(1)-C(6) ERYTHRONOLIDE FRAGMENT

Burke, Steven D.,Schoenen, Frank J.,Murtiashaw, Charles W.

, p. 449 - 452 (2007/10/02)

An enantioselective route to the C(1)-C(6) erythronolide unit 10 is described, involving the dioxanone-to-dihydropyran enolate Claisen rearrangement (78), regio- and stereoselective hydroboration to give 9a, and reductive fragmentation of the heterocyc

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