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N-(2-chlorophenyl)-4-(4-fluorophenyl)-1,3-thiazol-2-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61383-54-8

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61383-54-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61383-54-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,3,8 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 61383-54:
(7*6)+(6*1)+(5*3)+(4*8)+(3*3)+(2*5)+(1*4)=118
118 % 10 = 8
So 61383-54-8 is a valid CAS Registry Number.

61383-54-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-chlorophenyl)-4-(4-fluorophenyl)-1,3-thiazol-2-amine

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 -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:61383-54-8 SDS

61383-54-8Downstream Products

61383-54-8Relevant academic research and scientific papers

Antibacterial synergist, preparation method and uses thereof

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Paragraph 0254; 0257; 0258; 0259, (2018/03/28)

The present invention relates to an antibacterial synergist, a preparation method and uses thereof, and specifically discloses a compound represented by a formula (I) and having antibacterial synergyactivity, or an optical isomer, a cis-trans isomer or a pharmaceutically acceptable salt thereof, and a preparation method thereof. The present invention further discloses a medical composition containing the compound, and uses thereof. According to the present invention, the compound can effectively enhance the antibacterial activity of polymyxin B against Acinetobacter baumannii and Klebsiella pneumoniae, and can be used for the antibacterial treatment of pathogenic bacteria insensitive to polymyxin or having low bacterial inhibition activity. The formula (I) is defined in the specification.

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