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2-(benzoylamino)-3-(2,4-dimethoxyphenyl)prop-2-enoic acid is a propenoic acid derivative characterized by the presence of a benzoylamino group and a 2,4-dimethoxyphenyl group attached to its prop-2-enoic acid backbone. This chemical compound is widely recognized in the fields of medicinal chemistry and pharmaceutical research for its potential pharmacological properties and its utility as a building block in the synthesis of more complex molecules.

7149-95-3

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7149-95-3 Usage

Uses

Used in Medicinal Chemistry:
2-(benzoylamino)-3-(2,4-dimethoxyphenyl)prop-2-enoic acid is utilized as a key intermediate in the synthesis of various pharmaceutical compounds for its ability to contribute to the molecular structure and pharmacological activity of the final products.
Used in Pharmaceutical Research:
In pharmaceutical research, 2-(benzoylamino)-3-(2,4-dimethoxyphenyl)prop-2-enoic acid serves as a valuable component in the development of new drugs, potentially offering novel therapeutic options for various medical conditions due to its unique structural features and chemical properties.
Used in Drug Synthesis:
2-(benzoylamino)-3-(2,4-dimethoxyphenyl)prop-2-enoic acid is employed as a synthetic building block in the creation of diverse drug molecules, where its structural elements can be tailored to achieve specific biological activities and improve drug efficacy.
Used in Chemical Modification:
2-(benzoylamino)-3-(2,4-dimethoxyphenyl)prop-2-enoic acid is also used for the chemical modification of existing drugs to enhance their pharmacokinetic and pharmacodynamic profiles, potentially leading to improved therapeutic outcomes and reduced side effects.
Used in Biochemical Studies:
2-(benzoylamino)-3-(2,4-dimethoxyphenyl)prop-2-enoic acid is applied in biochemical studies to investigate its interactions with biological targets, providing insights into its potential mechanisms of action and applications in medicine.
Used in Drug Design:
In the field of drug design, 2-(benzoylamino)-3-(2,4-dimethoxyphenyl)prop-2-enoic acid is leveraged to create new molecular entities with optimized properties for drug development, including improved potency, selectivity, and safety profiles.

Check Digit Verification of cas no

The CAS Registry Mumber 7149-95-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,4 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7149-95:
(6*7)+(5*1)+(4*4)+(3*9)+(2*9)+(1*5)=113
113 % 10 = 3
So 7149-95-3 is a valid CAS Registry Number.

7149-95-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzamido-3-(2,4-dimethoxyphenyl)prop-2-enoic acid

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 -
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More Details:7149-95-3 SDS

7149-95-3Downstream Products

7149-95-3Relevant academic research and scientific papers

Nitrenium ion azaspirocyclization-spirodienone cleavage: A new synthetic strategy for the stereocontrolled preparation of highly substituted lactams and N-hydroxy lactams

Wardrop, Duncan J.,Burge, Matthew S.

, p. 10271 - 10284 (2007/10/03)

Although 1,4-cyclohexadienes 2, obtained through the Birch reduction of arenes 1, have found widespread use as masked β-oxo carbonyl synthons 3, the possibility that 2,5-cyclohexadienones 5 might also be employed to the same end has been overlooked despit

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