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99261-08-2

(3R,5S)-3-Allyl-3-{(S)-1-[2-(3,4,5-trimethoxy-phenyl)-[1,3]dithian-2-yl]-ethyl}-5-trityloxymethyl-dihydro-furan-2-one is a complex organic compound with a unique molecular structure. It consists of a dihydrofuran-2-one core, which is a type of cyclic ether, with a trityloxymethyl group at the 5-position, providing steric hindrance and stability. The molecule also features a 3-allyl group at the 3-position, which introduces a double bond and a carbon-carbon triple bond, contributing to its reactivity and potential applications in organic synthesis. The (S)-1-[2-(3,4,5-trimethoxy-phenyl)-[1,3]dithian-2-yl]-ethyl moiety is a chiral center, indicating that the compound has a specific three-dimensional arrangement of atoms. The presence of three methoxy groups on the phenyl ring suggests that the compound may have interesting electronic properties and potential applications in medicinal chemistry or as a precursor in the synthesis of other complex molecules. Overall, (3R,5S)-3-Allyl-3-{(S)-1-[2-(3,4,5-trimethoxy-phenyl)-[1,3]dithian-2-yl]-ethyl}-5-trityloxymethyl-dihydro-furan-2-one is a sophisticated example of organic chemistry, with potential uses in various fields due to its intricate structure and functional groups.

99261-08-2

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  • (3R,5S)-3-Allyl-3-{(S)-1-[2-(3,4,5-trimethoxy-phenyl)-[1,3]dithian-2-yl]-ethyl}-5-trityloxymethyl-dihydro-furan-2-one

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  • (3R,5S)-3-Allyl-3-{(S)-1-[2-(3,4,5-trimethoxy-phenyl)-[1,3]dithian-2-yl]-ethyl}-5-trityloxymethyl-dihydro-furan-2-one

    Cas No: 99261-08-2

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99261-08-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99261-08-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,2,6 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 99261-08:
(7*9)+(6*9)+(5*2)+(4*6)+(3*1)+(2*0)+(1*8)=162
162 % 10 = 2
So 99261-08-2 is a valid CAS Registry Number.

99261-08-2Downstream Products

99261-08-2Relevant articles and documents

ENANTIOSPECIFIC TOTAL SYNTHESIS OF (-)-MEGAPHONE BY A HIGHLY CONTROLLED CONSECUTIVE 1,4- AND 1,3-ASYMMETRIC INDUCTION.

Tomioka, Kiyoshi,Kawasaki, Hisashi,Iitaki, Yoichi,Koga, Kenji

, p. 903 - 906 (1985)

Enantiospecific total synthesis of (-)-megaphone (1) is reported.The key synthetic tactic is the use of (4S)-2Z-ethylidene-4-trityloxymethyl-butan-4-olide (6) to both establish the relative and absolute stereochemistry of the contiguous tertiary and quate

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