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4-(1-oxo-3-phenyl-2-propen-1-yl)benzeneacetic acid, also known as 4-(1-oxo-3-phenyl-2-propen-1-yl)benzeneacetic acid, is a complex organic compound with the chemical formula C16H14O3. This molecule features a benzene ring with a carboxylic acid group attached at the 4-position, and a 3-phenyl-2-propen-1-yl group (a phenylpropenyl group) attached to the 1-position of the benzene ring. The 1-oxo group indicates the presence of a carbonyl group, which is a double-bonded oxygen to a carbon atom. 4-(1-oxo-3-phenyl-2-propen-1-yl)benzeneacetic acid is characterized by its aromatic structure and the presence of a carbonyl group, which can participate in various chemical reactions, such as esterification or amidation. It is a white crystalline solid and is used in the synthesis of certain pharmaceuticals and other organic compounds due to its unique structure and reactivity.

3645-69-0

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3645-69-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3645-69-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,4 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3645-69:
(6*3)+(5*6)+(4*4)+(3*5)+(2*6)+(1*9)=100
100 % 10 = 0
So 3645-69-0 is a valid CAS Registry Number.

3645-69-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-(3-phenylacryloyl)phenyl)acetic 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

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More Details:3645-69-0 SDS

3645-69-0Relevant academic research and scientific papers

Anti-inflammatory Agents: Part IV - Synthesis and Anti-inflammatory Activity of 4-(5-Arylisoxazol-3-yl)phenylalkanoic Acids and Their Methyl Esters

Shridhar, D. R.,Sastry, C. V. Reddy,Bansal, O.P.,Singh, P. P.,Rao, C. Seshagiri

, p. 401 - 403 (2007/10/02)

The methyl esters (8a-d and 9a-d) of 4-(5-arylisoxazol-3-yl)phenylacetic and -phenyl-α-methylacetic acids (6a-d and 7a-d) have been synthesized from the corresponding chalkone dibromides (4a-d and 5a-d) by treatment with NH2OH.HCl in NaOH, followed by esterification of acids thus obtained.The anti-inflammatory activity of 6-9 has been evaluated.The most active compound 4-(5-phenylisoxazol-3-yl)phenyl-α-methylacetic acid (7a) showing 48.68percent inhibition is equipotent with phenylbutazone, but inactive in adjuvent induced arthritis test.

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