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ETHYL 2-[4-(TRIFLUOROMETHOXY)ANILINO]ACETATE is a chemical compound with the molecular formula C11H12F3NO3. It is an ethyl ester derivative of 2-[4-(trifluoromethoxy)anilino]acetic acid and is characterized by its unique structure that includes an ethyl group attached to a carboxylic acid group, which is connected to a trifluoromethoxy-anilino group through an amide linkage. This white solid is soluble in organic solvents such as methanol and ethanol and has a melting point of 72-74°C.

306935-79-5

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306935-79-5 Usage

Uses

Used in Pharmaceutical Industry:
ETHYL 2-[4-(TRIFLUOROMETHOXY)ANILINO]ACETATE is used as a building block for the synthesis of various bioactive compounds. Its unique structure and properties make it a valuable component in the development of new drugs and pharmaceuticals, contributing to the advancement of medical treatments and therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 306935-79-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,6,9,3 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 306935-79:
(8*3)+(7*0)+(6*6)+(5*9)+(4*3)+(3*5)+(2*7)+(1*9)=155
155 % 10 = 5
So 306935-79-5 is a valid CAS Registry Number.

306935-79-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name ETHYL 2-[4-(TRIFLUOROMETHOXY)ANILINO]ACETATE

1.2 Other means of identification

Product number -
Other names ethyl 2-{[4-(trifluoromethoxy)phenyl]amino}acetate

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:306935-79-5 SDS

306935-79-5Downstream Products

306935-79-5Relevant academic research and scientific papers

CASPASE 6 INHIBITORS AND USES THEREOF

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Paragraph 0612; 0669-0671, (2021/05/29)

Disclosed herein, inter alia, are compounds and methods for inhibiting Caspase 6 and the treatment of diseases, pharmaceutical composition including a compound as described herein and a pharmaceutically acceptable excipient and methods of inhibiting human Caspase 6 protein activity, the method including: contacting the human Caspase 6 protein with a compound as described herein.

Discovery and evolution of 12N-substituted aloperine derivatives as anti-SARS-CoV-2 agents through targeting late entry stage

Wang, Kun,Wu, Jia-Jing,Xin–Zhang,Zeng, Qing-Xuan,Zhang, Na,Huang, Wei-Jin,Tang, Sheng,Wang, Yan-Xiang,Kong, Wei-Jia,Wang, You-Chun,Li, Ying-Hong,Song, Dan-Qing

, (2021/08/03)

So far, there is still no specific drug against COVID-19. Taking compound 1 with anti-EBOV activity as the lead, fifty-four 12N-substituted aloperine derivatives were synthesized and evaluated for the anti-SARS-CoV-2 activities using pseudotyped virus model. Among them, 8a exhibited the most potential effects against both pseudotyped and authentic SARS-CoV-2, as well as SARS-CoV and MERS-CoV, indicating a broad-spectrum anti-coronavirus profile. The mechanism study disclosed that 8a might block a late stage of viral entry, mainly via inhibiting host cathepsin B activity rather than directly targeting cathepsin B protein. Also, 8a could significantly reduce the release of multiple inflammatory cytokines in a time- and dose-dependent manner, such as IL-6, IL-1β, IL-8 and MCP-1, the major contributors to cytokine storm. Therefore, 8a is a promising agent with the advantages of broad-spectrum anti-coronavirus and anti-cytokine effects, thus worthy of further investigation.

FERROCHELATASE INHIBITORS AND METHODS OF USE

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Page/Page column 62, (2019/11/19)

The invention relates to a method of treatment of a patient with a ferrochelatase inhibitor, or a pharmaceutically acceptable salt thereof, or a derivative thereof. Also, the invention relates to a method of treatment of a patient with a ferrochelatase in

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