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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 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 carbon-carbon double bond and enhances the compound's reactivity. Additionally, it contains a chiral center at the 3-position, with an (S)-1-[2-(3,4,5-trimethoxy-phenyl)-[1,3]dithian-2-yl]-ethyl substituent, which imparts optical activity and potential biological activity. The presence of three methoxy groups on the phenyl ring further contributes to the molecule's polarity and solubility properties. 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 represents a sophisticated example of organic chemistry, with potential applications in pharmaceuticals, materials science, or as a synthetic intermediate.

96851-85-3

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96851-85-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96851-85-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,8,5 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 96851-85:
(7*9)+(6*6)+(5*8)+(4*5)+(3*1)+(2*8)+(1*5)=183
183 % 10 = 3
So 96851-85-3 is a valid CAS Registry Number.

96851-85-3Downstream Products

96851-85-3Relevant academic research and scientific papers

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 (2007/10/02)

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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