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Ethanone, 2-chloro-1-(2-hydroxy-5-methylphenyl)(9CI), also known as 2-chloro-1-(2-hydroxy-5-methylphenyl)ethanone, is a chemical compound with the molecular formula C9H9ClO2. It is a derivative of acetophenone, featuring a chlorine atom and a hydroxy group attached to a phenyl ring. Ethanone, 2-chloro-1-(2-hydroxy-5-methylphenyl)(9CI) is widely used in organic synthesis and pharmaceutical research, making it an important intermediate in the production of various pharmaceuticals and related compounds. Its unique properties have also attracted interest in the field of medicinal chemistry for potential pharmacological and biological activities.

22307-94-4

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22307-94-4 Usage

Uses

Used in Pharmaceutical Industry:
Ethanone, 2-chloro-1-(2-hydroxy-5-methylphenyl)(9CI) is used as an intermediate in the synthesis of various pharmaceuticals and related compounds. Its unique structure and functional groups make it a valuable building block for the development of new drugs and therapeutic agents.
Used in Organic Synthesis:
In the field of organic synthesis, Ethanone, 2-chloro-1-(2-hydroxy-5-methylphenyl)(9CI) serves as a key intermediate for the preparation of a wide range of organic compounds. Its versatility in chemical reactions allows for the synthesis of various target molecules with potential applications in different industries.
Used in Medicinal Chemistry Research:
Ethanone, 2-chloro-1-(2-hydroxy-5-methylphenyl)(9CI) is utilized in medicinal chemistry research for the exploration of its potential pharmacological and biological activities. Its unique structure and functional groups make it an interesting candidate for the development of new therapeutic agents and the study of their mechanisms of action.

Check Digit Verification of cas no

The CAS Registry Mumber 22307-94-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,3,0 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 22307-94:
(7*2)+(6*2)+(5*3)+(4*0)+(3*7)+(2*9)+(1*4)=84
84 % 10 = 4
So 22307-94-4 is a valid CAS Registry Number.

22307-94-4SDS

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-Chloro-1-(2-hydroxy-5-methylphenyl)ethanone

1.2 Other means of identification

Product number -
Other names 2-hydroxy-5-methylphenacyl chloride

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:22307-94-4 SDS

22307-94-4Relevant academic research and scientific papers

Discovery of benzofuran-3(2H)-one derivatives as novel DRAK2 inhibitors that protect islet β-cells from apoptosis

Wang, Sheng,Xu, Lei,Lu, Yu-Ting,Liu, Yu-Fei,Han, Bing,Liu, Ting,Tang, Jie,Li, Jia,Wu, Jiangping,Li, Jing-Ya,Yu, Li-Fang,Yang, Fan

, p. 195 - 208 (2017/03/02)

Death-associated protein kinase-related apoptosis-inducing kinase-2 (DRAK2) is a serine/threonine kinase that plays a key role in a wide variety of cell death signaling pathways. Inhibition of DRAK2 was found to efficiently protect islet β-cells from apoptosis and hence DRAK2 inhibitors represent a promising therapeutic strategy for the treatment of diabetes. Only very few chemical entities targeting DRAK2 are currently known. We carried out a high throughput screening and identified compound 4 as a moderate DRAK2 inhibitor with an IC50value of 3.15?μM. Subsequent SAR studies of hit compound 4 led to the development of novel benzofuran-3(2H)-one series of DRAK2 inhibitors with improved potency and favorable selectivity profiles against 26 selected kinases. Importantly, most potent compounds 40 (IC50?=?0.33?μM) and 41 (IC50?=?0.25?μM) were found to protect islet β-cells from apoptosis in dose-dependent manners. These data support the notion that small molecule inhibitors of DRAK2 represents a promising strategy for the treatment of diabetes.

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