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(3R,5S)-3-Allyl-3-[2-(3,4,5-trimethoxy-phenyl)-[1,3]dithian-2-ylmethyl]-5-trityloxymethyl-dihydro-furan-2-one is a complex organic compound with a unique molecular structure. It features a dihydrofuran-2-one core, which is a type of cyclic ether with a carbonyl group. The compound has a 3-allyl group attached to the 3-position, providing it with a reactive allyl moiety. At the 5-position, there is a trityloxymethyl group, which is a bulky, electron-donating substituent that can influence the reactivity and physical properties of the molecule. The compound also contains a [1,3]dithiane ring, which is a sulfur-containing heterocycle, and a 3,4,5-trimethoxyphenyl group, which is a phenyl ring with three methoxy substituents. This intricate arrangement of functional groups and substituents gives the compound its specific chemical properties and potential applications in various fields, such as pharmaceuticals or materials science.

99261-10-6

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99261-10-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99261-10-6 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, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 99261-10:
(7*9)+(6*9)+(5*2)+(4*6)+(3*1)+(2*1)+(1*0)=156
156 % 10 = 6
So 99261-10-6 is a valid CAS Registry Number.

99261-10-6Downstream Products

99261-10-6Relevant academic research and scientific papers

CONTROL ELEMENTS IN THE ASYMMETRIC TANDEM ALKYLATION OF α-ALKYLIDENE-γ-BUTYROLACTONE DERIVATIVES

Tomioka, Kiyoshi,Kawasaki, Hisashi,Koga, Kenji

, p. 3027 - 3030 (2007/10/02)

Control elements in the highly selective construction of contiguous tertiary and quaternary carbon centers by the tandem alkylation of α-alkylidene-γ-butyrolactone derivatives were studied.It is clarified that the stereochemical course of the reaction is rationalized by evaluating highly selective 1,2-, 1,3-, and 1,4-asymmetric inductions.

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