107274-11-3 Usage
Class of compound
Ketones It belongs to the class of ketones, which are organic compounds with a carbonyl group (C=O) bonded to two carbon-containing groups.
Structure
Five-carbon chain with a ketone group and two phenyl groups The compound has a linear structure consisting of a five-carbon chain with a ketone group (C=O) at the first carbon and two phenyl groups (aromatic rings with a hydrogen atom attached to each carbon) attached to the first and fifth carbons.
Hydroxyl group
One of the phenyl groups has a hydroxyl (OH) group attached The phenyl group attached to the fifth carbon of the chain contains a hydroxyl group, which is a polar functional group that can form hydrogen bonds.
Precursor in synthesis
Commonly used as a precursor in the synthesis of other organic compounds Due to its unique structure, 1-Pentanone, 5-hydroxy-1,5-diphenylis often used as a starting material for the synthesis of more complex organic molecules.
Applications
Production of pharmaceuticals, fragrances, and dyes The compound is used in the production of various products, including pharmaceuticals, fragrances, and dyes, due to its ability to be converted into a wide range of organic compounds.
Industrial use
Solvent in various industrial processes 1-Pentanone, 5-hydroxy-1,5-diphenylis also used as a solvent in different industrial processes, taking advantage of its solubility and reactivity properties.
Building block for complex organic molecules
Unique structure and properties make it a valuable building block The compound's structure and properties make it an important intermediate for the synthesis of complex organic molecules, which can be further modified or functionalized to create a variety of products.
Check Digit Verification of cas no
The CAS Registry Mumber 107274-11-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,2,7 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 107274-11:
(8*1)+(7*0)+(6*7)+(5*2)+(4*7)+(3*4)+(2*1)+(1*1)=103
103 % 10 = 3
So 107274-11-3 is a valid CAS Registry Number.
107274-11-3Relevant articles and documents
Iron-Catalyzed Ring-Opening Reactions of Cyclopropanols with Alkenes and TBHP: Synthesis of 5-Oxo Peroxides
Lou, Chenhao,Wang, Xin,Lv, Leiyang,Li, Zhiping
, p. 7608 - 7612 (2021/10/02)
The ring opening of cyclopropanols is rarely used in multicomponent reactions. Herein we report the three-component reaction of cyclopropanols with alkenes and tert-butyl hydroperoxide (TBHP) catalyzed by an iron catalyst. This protocol enables the incorporation of both the β-carbonyl fragment and a peroxy unit across the C=C double bond regioselectively, thus allowing an efficient, facile access to 5-oxo peroxides. Modification of the biologically active molecules and various downstream derivatizations of the peroxides are also demonstrated.
Cobalt-catalyzed aerobic oxidation of (E)- and (Z)-bishomoallylic alcohols
Menéndez Pérez, Bárbara,Hartung, Jens
body text, p. 960 - 962 (2009/05/27)
Stereoselectivity for (5-phenyltetrahydrofur-2-yl)alkan-1-ol formation (cis:trans 1:99) from 5-methyl- and 5-phenyl-substituted 1-phenylpent-4-en-1-ols via cobalt-catalyzed aerobic oxidation was independent of the olefinic π-bond configuration of the su
Stereocontrol between remote atom centers in acyclic substrates. Anti addition of hydride to 1,5-, 1,6-, and 1,7-hydroxy ketones
Zhang, Han-Cheng,Harris, Bruce D.,Costanzo, Michael J.,Lawson, Edward C.,Maryanoff, Cynthia A.,Maryanoff, Bruce E.
, p. 7964 - 7981 (2007/10/03)
For conformationally unconstrained, acyclic organic compounds, the control of stereogenic centers at remote positions of a chain, that is, at a distance of four or more atom centers, remains a challenging problem in asymmetric synthesis. We report on our
