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α-Phenyl-α-hexyloxyacetophenone is a synthetic organic compound with the chemical formula C20H22O2. It is a derivative of acetophenone, featuring a phenyl group (C6H5) and a hexyloxy group (C6H13O) attached to the alpha carbon. α-Phenyl-α-hexyloxyacetophenone is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as in the production of dyes and pigments. Due to its complex structure, it is typically synthesized through multi-step chemical reactions, often involving the use of protective groups and careful control of reaction conditions to ensure the desired product is obtained. The compound's properties, such as its solubility and reactivity, can be influenced by the presence of the phenyl and hexyloxy groups, making it a versatile building block in organic chemistry.

22510-13-0

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22510-13-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22510-13-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,5,1 and 0 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 22510-13:
(7*2)+(6*2)+(5*5)+(4*1)+(3*0)+(2*1)+(1*3)=60
60 % 10 = 0
So 22510-13-0 is a valid CAS Registry Number.
InChI:InChI=1/C20H24O2/c1-2-3-4-11-16-22-20(18-14-9-6-10-15-18)19(21)17-12-7-5-8-13-17/h5-10,12-15,20H,2-4,11,16H2,1H3

22510-13-0SDS

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 2-Hexyloxy-1,2-diphenylethanone

1.2 Other means of identification

Product number -
Other names -

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:22510-13-0 SDS

22510-13-0Relevant articles and documents

Probing the Binding Pocket of the Broadly Tuned Human Bitter Taste Receptor TAS2R14 by Chemical Modification of Cognate Agonists

Karaman, Rafik,Nowak, Stefanie,Di Pizio, Antonella,Kitaneh, Hothaifa,Abu-Jaish, Alaa,Meyerhof, Wolfgang,Niv, Masha Y.,Behrens, Maik

, p. 66 - 75 (2016/07/09)

Sensing potentially harmful bitter substances in the oral cavity is achieved by a group of ?25 receptors, named TAS2Rs, which are expressed in specialized sensory cells and recognize individual but overlapping sets of bitter compounds. The receptors differ in their tuning breadths ranging from narrowly to broadly tuned receptors. One of the most broadly tuned human bitter taste receptors is the TAS2R14 recognizing an enormous variety of chemically diverse synthetic and natural bitter compounds, including numerous medicinal drugs. This suggests that this receptor possesses a large readily accessible ligand binding pocket. To allow probing the accessibility and size of the ligand binding pocket, we chemically modified cognate agonists and tested receptor responses in functional assays. The addition of large functional groups to agonists was usually possible without abolishing agonistic activity. The newly synthesized agonist derivatives were modeled in the binding site of the receptor, providing comparison to the mother substances and rationalization of the in vitro activities of this series of compounds.

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