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(2E)-3-Phenyl-N-(4-phenyl-1,3-thiazol-2-yl)-2-propenamide is a chemical compound that belongs to the class of thiazole derivatives. It is a yellow solid with a molecular formula of C18H13N3OS. (2E)-3-Phenyl-N-(4-phenyl-1,3-thiazol-2-yl)-2-propenamide is commonly used in the field of medicinal chemistry, where it exhibits potential pharmacological activities. Its structure contains a thiazole ring and a phenyl group, which are important for its biological activity.

74675-87-9

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74675-87-9 Usage

Uses

Used in Pharmaceutical Industry:
(2E)-3-Phenyl-N-(4-phenyl-1,3-thiazol-2-yl)-2-propenamide is used as a pharmaceutical candidate for its potential anti-inflammatory, antifungal, and antibacterial properties. Its unique structure and biological activities make it a promising agent for further research and development in the pharmaceutical industry.
Used in Medicinal Chemistry Research:
(2E)-3-Phenyl-N-(4-phenyl-1,3-thiazol-2-yl)-2-propenamide is used as a research compound to study its various biological activities and potential applications in medicinal chemistry. Its structure and properties allow for the exploration of its therapeutic potential in treating various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 74675-87-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,6,7 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 74675-87:
(7*7)+(6*4)+(5*6)+(4*7)+(3*5)+(2*8)+(1*7)=169
169 % 10 = 9
So 74675-87-9 is a valid CAS Registry Number.

74675-87-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenyl-N-(4-phenyl-1,3-thiazol-2-yl)prop-2-enamide

1.2 Other means of identification

Product number -
Other names 2-Cinnamamido-4-phenylthiazole

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:74675-87-9 SDS

74675-87-9Relevant academic research and scientific papers

Microwave assisted synthesis of some thiazolyl-pyrazoline and N-phenyl-2-pyrazoline derivatives over potassium carbonate

Baviskar,Deore,Khadabadi

, p. 239 - 244 (2013/06/05)

In the present study, a series of twenty new N-(1,5-diphenyl-4,5-dihydro- 1H-3-pyrazolyl)-N-(4-phenyl-1,3-thiazol-2-yl)amine (4a-j) and N-(5-phenyl-4,5-dihydro-1H-3-pyrazolyl)-N-(4-phenyl-1,3-thiazol-2-yl)amine (5a-j) have been synthesized in 70-85% yield by a microwave-assisted solvent-free condensation of N1-(4-phenyl-1,3-thiazol-2-yl)-(Z)-3-phenyl-2- propenamide (3a-j) with hydrazine hydrate/N-phenylhydrazine in ethanol over potassium carbonate. The reaction condition is simple, involves the treatment of ice-cold water and eliminates the usage of solvent. The reaction time is minimizes from hours to minutes with increase in yield.

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