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1-(toluene-4-sulfonyloxy)-2-(2,3,3-trimethyl-cyclopent-1-enyl)-ethane is a complex organic compound with the molecular formula C18H24O3S. It features a toluene-4-sulfonyl group attached to the first carbon atom of an ethane chain, while the second carbon atom is connected to a 2,3,3-trimethyl-cyclopent-1-enyl group. 1-(toluene-4-sulfonyloxy)-2-(2,3,3-trimethyl-cyclopent-1-enyl)-ethane is characterized by its unique structure, which includes a cyclopentane ring with three methyl groups and a double bond, as well as a sulfonyl ether linkage. It is likely to be found in specialized chemical research or industrial applications due to its specific functional groups and structural features.

2565-75-5

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2565-75-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2565-75-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,6 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2565-75:
(6*2)+(5*5)+(4*6)+(3*5)+(2*7)+(1*5)=95
95 % 10 = 5
So 2565-75-5 is a valid CAS Registry Number.

2565-75-5Downstream Products

2565-75-5Relevant academic research and scientific papers

Synthesis and Reactions of β-Camphole Compounds

Schulze, K.,Wyssuwa, K.,Trauer, H.,Habermann, A.-K.

, p. 537 - 543 (1993)

In contrast to the well known α-campholenic (B) and fencholenic compounds (C) little is known about β-campholenic derivatives (A) because of their difficult accessibility. β-Campholenic compounds (A) can be obtained: (1) by Baeyer-Villiger oxidation of camphor via lactone 7 and β-dihydrocampholenic lactone (5); (2) by Beckmann fragmentation of camphor oxime via α-(2) and β-campholenic nitril (3) and the lactone 5; and (3) by acid catalysed rearrangement of α-campholenic derivatives (B, 17a, b).The β-analogous brahmanol (14) can be synthesized by the reaction of the β-campholenic bromide (11) with methyl diethyl malonate or by r earrangement of brahmanol.

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