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N-[2-(trifluoromethyl)phenyl]dodecanamide is a complex organic compound with the chemical formula C18H22F3NO. It is a derivative of dodecanamide, featuring a phenyl ring with a trifluoromethyl group at the 2-position and an amide group attached to the nitrogen atom. N-[2-(trifluoromethyl)phenyl]dodecanamide is characterized by its lipophilic nature due to the presence of the trifluoromethyl group, which can enhance its solubility in nonpolar solvents. It may have potential applications in various fields, such as pharmaceuticals or chemical research, where its unique structure could influence its interactions with biological targets or other molecules. The specific properties and uses of N-[2-(trifluoromethyl)phenyl]dodecanamide would depend on its ability to form hydrogen bonds, its electronic properties, and its reactivity, which are influenced by the presence of the trifluoromethyl group and the amide functionality.

2803-96-5

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2803-96-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2803-96-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,0 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2803-96:
(6*2)+(5*8)+(4*0)+(3*3)+(2*9)+(1*6)=85
85 % 10 = 5
So 2803-96-5 is a valid CAS Registry Number.

2803-96-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name lauric acid-(2-trifluoromethyl-anilide)

1.2 Other means of identification

Product number -
Other names lauric acid-(2-dimethylamino-ethyl ester),hydrochloride

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:2803-96-5 SDS

2803-96-5Upstream product

2803-96-5Downstream Products

2803-96-5Relevant academic research and scientific papers

INHIBITORS OF BIOFILM FORMATION OF GRAM-POSITIVE AND GRAM-NEGATIVE BACTERIA

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Page/Page column 46-47; 51-52, (2009/07/18)

The present invention relates to the use of compounds as broad spectrum inhibitors of bacterial biofilm formation. In particular the invention refers to a family of compounds that block the quorum sensing system of Gram-negative and Gram-positive bacteria, a process for their manufacture, pharmaceutical compositions containing them and to their use for the treatment and prevention of bacterial damages and diseases, in particular for diseases where there is an advantage in inhibiting quorum sensing regulated phenotypes of pathogens.

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