156634-92-3 Usage
Explanation
Different sources of media describe the Explanation of 156634-92-3 differently. You can refer to the following data:
1. The molecular formula represents the number of atoms of each element present in a molecule of the compound.
2. The compound is derived from piperidine, a heterocyclic amine, and contains a sulfonyl group (-SO2-) and a chlorophenyl group (C6H4Cl) attached to it.
3. The compound has shown potential pharmacological activity, which means it may have beneficial effects on biological systems and could be used for therapeutic purposes.
4. Due to its unique structure and potential biological activity, the compound may have uses in the fields of medicine for treating various conditions and in chemical research for further understanding of its properties and applications.
5. While the compound has shown potential, more research is required to fully understand its properties, potential applications, and any possible side effects or limitations.
6. The specific chemical properties of 1-[(4-chlorophenyl)sulfonyl]piperidin-4-one, such as solubility, reactivity, or stability, are not provided in the given material and would require further investigation.
7. The specific physical properties of the compound, such as appearance, melting point, or boiling point, are not provided in the given material and would require further investigation.
Chemical structure
Piperidine derivative with a sulfonyl group and a chlorophenyl group
Pharmacological activity
Potential therapeutic applications
Fields of application
Medicine and chemical research
Research status
Further research needed
Chemical properties
Unknown (based on the provided material)
Physical properties
Unknown (based on the provided material)
Check Digit Verification of cas no
The CAS Registry Mumber 156634-92-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,6,3 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 156634-92:
(8*1)+(7*5)+(6*6)+(5*6)+(4*3)+(3*4)+(2*9)+(1*2)=153
153 % 10 = 3
So 156634-92-3 is a valid CAS Registry Number.
156634-92-3Relevant articles and documents
Stereoselective Dehydroxyboration of Allylic Alcohols to Access (E)-Allylboronates by a Combination of C-OH Cleavage and Boron Transfer under Iron Catalysis
Su, Wei,Wang, Ting-Ting,Tian, Xia,Han, Jian-Rong,Zhen, Xiao-Li,Fan, Shi-Ming,You, Ya-Xin,Zhang, Yu-Kun,Qiao, Rui-Xiao,Cheng, Qiushi,Liu, Shouxin
supporting information, p. 9094 - 9099 (2021/11/30)
Iron-catalyzed direct SN2′ dehydroxyboration of allylic alcohols has been developed to access (E)-stereoselective allylboronates. Allylic alcohols with diverse structures and functional groups, especially derived from natural products, underwent smooth transformation. The six-membered ring transition state formed by allylic alcohols and iron-boron intermediate was indicated to be the key component involved in transfer of the boron group, activation of the C-OH bond, and control of the stereoselectivity.
DISPIRO TETRAOXANE COMPOUNDS
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Page/Page column 79, (2008/06/13)
A compound having the formula (I) wherein ring A represents a substituted or unsubstituted monocyclic or multicyclic ring; m=any positive integer; n=0-5; X=CH and Y=-C(O)NR1R2, -NR1R2 or -S(O)2R4, where R1, R2 and R4 are each individually selected from the group consisting of H, substituted or unsubstituted alkyl, substituted or unsubstituted aryl, substituted or unsubstituted amine, substituted or unsubstituted carbocyclic ring, substituted or unsubstituted heterocyclic ring, or any combination thereof, or R1 and R2 are linked so as to form part of a substituted or unsubstituted heterocyclic ring, or X=N and Y=-S(O)2R3 or -C(O)R3, where R3 is selected from the group consisting of H, substituted or unsubstituted alkyl, substituted or unsubstituted aryl, substituted or unsubstituted amine, substituted or unsubstituted carbocyclic ring, substituted or unsubstituted heterocyclic ring or any combination thereof.
