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<α-Brom-cyclopentyl>-p-tolyl-keton is a chemical compound characterized by its molecular structure, which features a cyclopentyl ring with an α-bromine substituent and a p-tolyl (4-methylphenyl) group attached to a ketone functional group. This organic molecule is a derivative of cyclopentanone, with the bromine atom and p-tolyl group providing unique electronic and steric properties that can influence its reactivity and physical characteristics. The compound may be used in the synthesis of various pharmaceuticals, agrochemicals, or other specialty chemicals due to its potential to act as an intermediate or a building block in organic synthesis. Its specific applications and properties would depend on the context in which it is used, and further research or experimentation would be necessary to explore its full potential.

6758-17-4

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6758-17-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6758-17-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,5 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6758-17:
(6*6)+(5*7)+(4*5)+(3*8)+(2*1)+(1*7)=124
124 % 10 = 4
So 6758-17-4 is a valid CAS Registry Number.

6758-17-4Downstream Products

6758-17-4Relevant academic research and scientific papers

Catalytic Asymmetric Acyloin Rearrangements of α-Ketols, α-Hydroxy Aldehydes, and α-Iminols by N, N′-Dioxide-Metal Complexes

Dai, Li,Li, Xiangqiang,Zeng, Zi,Dong, Shunxi,Zhou, Yuqiao,Liu, Xiaohua,Feng, Xiaoming

, p. 5041 - 5045 (2020/07/03)

A highly enantioselective acyloin rearrangement of cyclic α-ketols has been developed with a chiral Al(III)-N,N′-dioxide complex as catalyst. This strategy provided an array of optically active 2-acyl-2-hydroxy cyclohexanones in moderate to good yields with high enantioselectivities. The asymmetric isomerizations of acyclic α-hydroxy aldehydes and α-iminols were achieved as well under modified conditions, affording the corresponding chiral α-hydroxy ketones and α-amino ketones in moderate results. Moreover, further transformations of product to enantioenriched diols were carried out.

Iron-Catalyzed Acyl Migration of Tertiary α-Azidyl Ketones: Synthetic Approach toward Enamides and Isoquinolones

Yang, Tonghao,Fan, Xing,Zhao, Xiaopeng,Yu, Wei

supporting information, p. 1875 - 1879 (2018/04/16)

This paper reports that tertiary α-azidyl phenyl ketones can be transformed into enamides by treatment with FeBr2 at elevated temperature in DMF. The reaction proceeds via 1,2-benzoyl migration from α-carbon to the nitrogen atom, accompanied by expulsion of a nitrogen molecule. This protocol is suitable for the synthesis of N-(cyclopent-1-en-1-yl)benzamides, N-(cyclohex-1-en-1-yl)benzamides, and N-benzoyl-α-methyl enamines and provides a convenient approach toward isoquinolones.

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