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2H-Pyran-3-carboxylic acid, 6-(4-chlorophenyl)-4-(methylthio)-2-oxo-, ethyl ester is an organic compound characterized by a complex structure that features a pyran ring, a carboxylic acid group, a 4-chlorophenyl group, a methylthio group, and an ethyl ester functional group. This unique molecular architecture endows the compound with potential pharmaceutical and industrial applications, largely due to its capacity for biological activity. The presence of the ester group indicates that it could function as a prodrug, serving as a precursor to an active pharmaceutical agent that is metabolized in the body to release the active drug. Further investigation and experimentation are required to ascertain the specific characteristics and possible applications of this chemical.

153391-45-8

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153391-45-8 Usage

Uses

Used in Pharmaceutical Industry:
2H-Pyran-3-carboxylic acid, 6-(4-chlorophenyl)-4-(methylthio)-2-oxo-, ethyl ester is used as a prodrug for its potential to be metabolized in the body to release an active pharmaceutical compound. 2H-Pyran-3-carboxylic acid, 6-(4-chlorophenyl)-4-(methylthio)-2-oxo-,
ethyl ester's unique structure, including the pyran ring and various functional groups, suggests that it may possess specific biological activities that could be harnessed for therapeutic purposes.
Used in Chemical Research:
In the field of chemical research, 2H-Pyran-3-carboxylic acid, 6-(4-chlorophenyl)-4-(methylthio)-2-oxo-, ethyl ester serves as a subject of study for understanding the synthesis, reactivity, and potential applications of complex organic molecules. Its structure may offer insights into new chemical reactions or pathways, contributing to the advancement of organic chemistry.
Used in Industrial Applications:
Although specific industrial uses are not detailed in the provided materials, the compound's unique structure and functional groups could make it a candidate for various industrial applications, such as in the development of new materials, catalysts, or as intermediates in the synthesis of other complex organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 153391-45-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,3,9 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 153391-45:
(8*1)+(7*5)+(6*3)+(5*3)+(4*9)+(3*1)+(2*4)+(1*5)=128
128 % 10 = 8
So 153391-45-8 is a valid CAS Registry Number.

153391-45-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 6-(4-chlorophenyl)-4-(methylthio)-2-oxo-2H-pyran-3-carboxylate

1.2 Other means of identification

Product number -
Other names 2H-Pyran-3-carboxylic acid, 6-(4-chlorophenyl)-4-(methylthio)-2-oxo-,ethyl ester

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:153391-45-8 SDS

153391-45-8Relevant academic research and scientific papers

Polysubstituted 2H-pyran-2-ones: A new class of hepatoprotective agents

Ram, Vishnu J.,Haque, Navedul,Nath, Mahendra,Singh, Sunil K.,Hussaini, Falak A.,Tripathi,Shoeb

, p. 3149 - 3152 (2007/10/03)

The synthesis and hepatoprotective activity of 6-aryl-3-substituted-4-methylthio-2H-pyran-2-ones (3, 5, 7) and the corresponding 2-thiones (6), 6-aryl-4-methylthio-2H-pyran-2-ones (4) and 6-aryl-3-carbethoxy-5-cyano-4-methylthio-2H-pyran-2-ones are described.

Ring transformation reaction: Part II - Reaction specificity of hydrazines towards 6-aryl-4-(methylthio)-2-oxo-2H-pyran-3-carbonitriles and corresponding 3-ethyl carboxylate

Ram, Vishnu Ji,Haque, Navedul,Singh, Sanjay Kumar,Hussaini, Falak Anwer,Shoeb, Aboo

, p. 924 - 928 (2007/10/02)

Reaction specificity of hydrazine hydrate, cyclohexyl- and phenyl-hydrazines towards 6- or 5,6-disubstituted-4-(methylthio)-2-oxo-2H-pyran-3-carbonitriles and the corresponding 3-ethyl carboxylate (1,8) has been studied.

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