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(1R,2S)-1-Dodecyl-2-methyl-cyclopropane is a chiral organic compound with a unique structure, consisting of a cyclopropane ring with a dodecyl group attached to the first carbon and a methyl group attached to the second carbon. (1R,2S)-1-Dodecyl-2-methyl-cyclopropane is characterized by its three-carbon ring, which is a strained cyclic structure, and the presence of two chiral centers, resulting in four possible stereoisomers. The specific configuration of (1R,2S)-1-Dodecyl-2-methyl-cyclopropane, with the dodecyl group on the R side and the methyl group on the S side, gives it distinct physical and chemical properties compared to its other isomers. It is an example of a complex organic molecule that can be found in various chemical and pharmaceutical applications, where stereochemistry plays a crucial role in its reactivity and biological activity.

82044-55-1

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82044-55-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82044-55-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,0,4 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 82044-55:
(7*8)+(6*2)+(5*0)+(4*4)+(3*4)+(2*5)+(1*5)=111
111 % 10 = 1
So 82044-55-1 is a valid CAS Registry Number.

82044-55-1Downstream Products

82044-55-1Relevant academic research and scientific papers

New Synthesis of Cyclopropanes from 1,3-Dicarbonyl Compounds Utilizing Electroreduction of 1,3-Dimethanesulfonates

Shono, Tatsuyo,Matsumura, Yoshihiro,Tsubata, Kenji,Sugihara, Yoshihiro

, p. 3090 - 3094 (1982)

Electroorganic synthesis of cyclopropanes from dimethanesulfonates of 1,3-diols is described.The process involves reduction of 1,3-dicarbonyl compounds with LiAlH followed by esterification with methanesulfonyl chloride and electroreduction.

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