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(2R,3R)-2,4-dimethylheptyl tosylate is a chiral organic compound with the molecular formula C14H24O3S. It is a derivative of heptane, featuring two methyl groups at the 2nd and 4th carbon positions, and a tosyl (tosylate) group attached to the hydroxyl group at the 1st carbon. The compound exhibits two chiral centers, resulting in four possible stereoisomers. The specific (2R,3R) configuration indicates that both chiral centers have the R (rectus) configuration. (2R,3R)-2,4-dimethylheptyl tosylate is primarily used in organic synthesis, particularly in the preparation of complex molecules and pharmaceuticals, due to its unique stereochemistry and reactivity.

18450-75-4

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18450-75-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18450-75-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,4,5 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 18450-75:
(7*1)+(6*8)+(5*4)+(4*5)+(3*0)+(2*7)+(1*5)=114
114 % 10 = 4
So 18450-75-4 is a valid CAS Registry Number.

18450-75-4Downstream Products

18450-75-4Relevant academic research and scientific papers

STEREOCHEMISTRY OF LARDOLURE. THE AGGREGATION PHEROMONE OF THE ACARID MITE, LARDOGLYPHUS KONOI

Mori, Kenji,Kuwahara, Shigefumi

, p. 5545 - 5550 (2007/10/02)

(1R,3R,5R,7R)-Stereochemistry was assigned to lardolure (1,3,5,7-tetramethyldecyl formate) on the basis of GLC comparison of the natural pheromone with the synthetic pheromones prepared in partially stereocontrolled manners.

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