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3-oxaspiro[5.5]undecan-2-one is a cyclic ketone with a unique structure, characterized by a spiro carbon atom connecting two rings. This organic compound consists of a six-membered carbon ring fused to a five-membered ring containing an oxygen atom, forming a spiro structure. The ketone functional group is located at the 3-position, which is adjacent to the spiro carbon. 3-oxaspiro[5.5]undecan-2-one is of interest in organic chemistry due to its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its role as an intermediate in the preparation of complex organic molecules. Its chemical properties, such as reactivity and stability, are influenced by the presence of the spiro structure and the ketone group, making it a subject of study for chemists exploring the behavior of such unique molecular architectures.

6051-08-7

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6051-08-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6051-08-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,5 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6051-08:
(6*6)+(5*0)+(4*5)+(3*1)+(2*0)+(1*8)=67
67 % 10 = 7
So 6051-08-7 is a valid CAS Registry Number.

6051-08-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-oxaspiro[5.5]undecan-4-one

1.2 Other means of identification

Product number -
Other names 3-OXASPIRO(5,5)UNDECAN-2-ONE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6051-08-7 SDS

6051-08-7Relevant academic research and scientific papers

Catalytic Asymmetric Synthesis of Cyclohexanes by Hydrogen Borrowing Annulations

Armstrong, Roly J.,Akhtar, Wasim M.,Young, Tom A.,Duarte, Fernanda,Donohoe, Timothy J.

supporting information, p. 12558 - 12562 (2019/08/16)

Hydrogen borrowing catalysis serves as a powerful alternative to enolate alkylation, enabling the direct coupling of ketones with unactivated alcohols. However, to date, methods that enable control over the absolute stereochemical outcome of such a process have remained elusive. Here we report a catalytic asymmetric method for the synthesis of enantioenriched cyclohexanes from 1,5-diols via hydrogen borrowing catalysis. This reaction is mediated by the addition of a chiral iridium(I) complex, which is able to impart high levels of enantioselectivity upon the process. A series of enantioenriched cyclohexanes have been prepared and the mode of enantioinduction has been probed by a combination of experimental and DFT studies.

Radical C(sp2)-H Trifluoromethylation of Aldehydes in Aqueous Solution

Zhang, Pei,Shen, Haigen,Zhu, Lin,Cao, Weiguo,Li, Chaozhong

supporting information, p. 7062 - 7065 (2018/11/21)

The copper-mediated C(sp2)-H trifluoromethylation of aldehydes is described. The reaction of aldehydes with (bpy)Cu(CF3)3, Et3SiH, and K2S2O8 in aqueous acetone at room temperatu

NOVEL 4-(2FUROYL)AMINOPIPERIDINES, INTERMEDIATES IN SYNTHESIZING THE SAME,PROCESS FOR PRODUCING THE SAME AND MEDICINAL USE OF THE SAME

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Page 35, (2008/06/13)

There are provided novel 4-(2-furoyl)aminopiperidines represented by the general formula (I), their synthetic intermediates, processes for their preparation and medicaments containing them. In the above formula, X is CH or N, and Y is a group of the following general formula (II), formula (II-a) or formula (III): wherein a, b and c are each an integer of 0-6; Z is CH2 or NH; W is O or S; T is O or N-R15 wherein R15 is H, a C1-C6 alkyl group, a benzyl group or a phenethyl group; and R1 is H, a C1-C6 alkoxycarbonyl group, a benzyloxycarbonyl group, or the like.The 4-(2-furoyl) aminopiperidine derivatives according to this invention possess opioid μ antagonistic activity and are useful for the treatment or prevention of side effects which are caused by μ receptors agonist and which are selected from constipation, nausea/emesis or itch, or for the treatment or prevention of idiopathic constipation, postoperative ileus, paralytic ileus, irritable bowel syndrome or chronic pruritus.

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