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1-p-Anisyl-2-adamantyl tosylates are a class of organic compounds that consist of a tosyl group (tosylate) attached to a molecule containing a p-anisyl (para-methoxyphenyl) group and an adamantyl group. The p-anisyl group is a substituted phenyl ring with a methoxy group at the para position, while the adamantyl group is a highly branched and rigid hydrocarbon structure derived from adamantane. These compounds are of interest in various fields, including chemistry, materials science, and pharmaceuticals, due to their unique structural properties and potential applications in the synthesis of complex molecules and the development of new drugs. The tosyl group, in particular, is known for its reactivity and ability to act as a protecting group in organic synthesis, making 1-p-anisyl-2-adamantyl tosylates valuable intermediates in the preparation of various target compounds.

40571-21-9

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40571-21-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40571-21-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,5,7 and 1 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 40571-21:
(7*4)+(6*0)+(5*5)+(4*7)+(3*1)+(2*2)+(1*1)=89
89 % 10 = 9
So 40571-21-9 is a valid CAS Registry Number.

40571-21-9Downstream Products

40571-21-9Relevant academic research and scientific papers

SOLVOLYSIS OF 3-SUBSTITUTED 4-HOMOADAMANTYL METHANESULPHONATES. CAN THE β-SUBSTITUENT EFFECT DISTINGUISH BETWEEN CLASSICAL AND NON-CLASSICAL ION INTERMEDIATES ?

Okazaki, Takao,Kitagawa, Toshikazu,Takeuchi, Ken'Ichi

, p. 485 - 494 (1994)

The rates of the solvolysis of 3-R-4-homoadamantyl methanesulphonates (mesylates) (3) were determined in 80percent aqueous ethanol.The relative first-order rate constants at 25 deg C were 1.0 (R=H), 2.29 (R=Ph), 3.26 (R=p-anisyl), 73.6 (R=Me) and 209 (R=E

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