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Methyl (3-acetylphenoxy)acetate, also known as 1-acetyl-2-(3-acetylphenoxy)ethane, is an organic compound with the chemical formula C11H12O4. It is a colorless to pale yellow liquid with a molecular weight of 208.21 g/mol. This ester derivative is characterized by the presence of an acetyl group (-COCH3) attached to a phenoxy ring, which is further connected to a methyl ester group (-COOCH3). Methyl (3-acetylphenoxy)acetate is synthesized through the reaction of 3-acetylphenol with methyl acetoacetate and is used as an intermediate in the production of various pharmaceuticals and agrochemicals. It is also known for its potential applications in the synthesis of dyes and other specialty chemicals.

6951-35-5

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6951-35-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6951-35-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,5 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6951-35:
(6*6)+(5*9)+(4*5)+(3*1)+(2*3)+(1*5)=115
115 % 10 = 5
So 6951-35-5 is a valid CAS Registry Number.

6951-35-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-Acetyl-phenoxy)-essigsaeure-methylester

1.2 Other means of identification

Product number -
Other names (3-acetyl-phenoxy)-acetic acid

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:6951-35-5 SDS

6951-35-5Relevant academic research and scientific papers

Development of non-ethoxypropanoic acid type cryptochrome inhibitors with circadian molecular clock-enhancing activity by bioisosteric replacement

Jeong, Yong Uk,Jin, Hyo-Eon,Lim, Hye Young,Choi, Goyeong,Joo, Hansol,Kang, Bohun,Lee, Ga-Hyun,Liu, Kwang-Hyeon,Maeng, Han-Joo,Chung, Sooyoung,Son, Gi Hoon,Jung, Jong-Wha

, (2021)

Circadian dysfunction is closely associated with an increased risk of various diseases. Considering that molecular clock machinery serves as an intrinsic time-keeping system underlying the circadian rhythm of biological processes, the modulation of the mo

2-Amido-thiazole-based compounds exhibiting ATP-utilizing enzyme inhibitory activity, and compositions, and uses thereof

-

Page/Page column 25-26, (2008/06/13)

2-Amido-4-substituted-aryl-thiazole-based compounds exhibiting ATP-utilizing enzyme inhibitory activity, methods of using compounds exhibiting ATP-utilizing enzyme inhibitory activity, and compositions comprising compounds exhibiting ATP-utilizing enzyme

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