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(1R,2S)-1-Phenylselanyl-1-((1R,5R)-5-vinyl-cyclopent-2-enyl)-butan-2-ol is a complex organic compound characterized by its unique stereochemistry and structure. It features a chiral carbon center, with the R configuration at both the 1st and 2nd positions, indicating that the substituents are arranged in a specific three-dimensional orientation. The molecule consists of a phenylselanyl group attached to a butan-2-ol backbone, which is further connected to a cyclopent-2-enyl ring through a vinyl bridge. This cyclopent-2-enyl ring also has a chiral center with the R configuration at the 5th position, adding to the molecule's complexity. The compound's structure is stabilized by the presence of a double bond within the cyclopent-2-enyl ring, which contributes to its reactivity and potential applications in various chemical and pharmaceutical contexts.

78780-96-8

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78780-96-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78780-96-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,7,8 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 78780-96:
(7*7)+(6*8)+(5*7)+(4*8)+(3*0)+(2*9)+(1*6)=188
188 % 10 = 8
So 78780-96-8 is a valid CAS Registry Number.

78780-96-8Downstream Products

78780-96-8Relevant academic research and scientific papers

Total Synthesis of (+/-)-Multifidene, the Gamete Attractant of the Phaeophyte Cutleria multifida

Crouse, Gary D.,Paquette, Leo A.

, p. 4272 - 4274 (2007/10/02)

A short, stereoselective total synthesis of racemic multifidene has been achieved.The key elements of the synthetic scheme are (i) oxyanionic Cope rearrangement of cis3-2,4,7-cyclononatrienol and in situ trapping of the resulting enolate with chlorotrimethylsilane, (ii) stereocontrolled introduction of a phenylseleno group α to the aldehyde functionality, (iii) addition of an ethyl fragment under conditions where the polar PhSe substituent can induce high levels of stereoselection, and (iv) a double inversion sequence to introduce a cis double bond cleanly.

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