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2,2,2-Trifluoro-N-(2-hydroxy-4-nitrophenyl)-acetamide is a chemical compound with the molecular formula C8H6F3N3O4. It is a derivative of acetamide, featuring a trifluoromethyl group, a nitrophenyl group, and a hydroxy group. 2,2,2-Trifluoro-N-(2-hydroxy-4-nitrophenyl)-acetamide is utilized in the field of medicinal chemistry, particularly for the development of pharmaceuticals and agrochemicals. Its structural features and functional groups may endow it with potential applications as an antimicrobial or antifungal agent. The synthesis and study of 2,2,2-Trifluoro-N-(2-hydroxy-4-nitrophenyl)-acetamide could contribute to the advancement of new drugs and biologically active molecules. However, due to its potential reactivity and toxicity, it is crucial to handle this chemical with care and adhere to proper safety protocols.

785-27-3

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785-27-3 Usage

Uses

Used in Medicinal Chemistry:
2,2,2-Trifluoro-N-(2-hydroxy-4-nitrophenyl)-acetamide is used as a building block in the synthesis of pharmaceuticals for its unique structural features and functional groups that may contribute to the development of new drugs with specific therapeutic properties.
Used in Agrochemical Development:
In the agrochemical industry, 2,2,2-Trifluoro-N-(2-hydroxy-4-nitrophenyl)-acetamide is used as a precursor in the creation of new agrochemicals, potentially serving as an antimicrobial or antifungal agent to protect crops and enhance agricultural productivity.
Used in Antimicrobial Agents:
2,2,2-Trifluoro-N-(2-hydroxy-4-nitrophenyl)-acetamide is used as an antimicrobial agent for its potential to combat various microorganisms, leveraging its structural features to inhibit microbial growth and reduce the spread of infections.
Used in Antifungal Agents:
Similarly, in the realm of antifungal agents, 2,2,2-Trifluoro-N-(2-hydroxy-4-nitrophenyl)-acetamide is utilized to target and control fungal infections, capitalizing on its chemical properties to disrupt fungal cell functions and prevent their proliferation.

Check Digit Verification of cas no

The CAS Registry Mumber 785-27-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,8 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 785-27:
(5*7)+(4*8)+(3*5)+(2*2)+(1*7)=93
93 % 10 = 3
So 785-27-3 is a valid CAS Registry Number.

785-27-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,2-Trifluoro-N-(2-hydroxy-4-nitrophenyl)acetamide

1.2 Other means of identification

Product number -
Other names trifluorohydroxynitrophenylacetamide

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:785-27-3 SDS

785-27-3Relevant academic research and scientific papers

Stepwise and one-pot cross-coupling-heteroannulation approaches toward 2-substituted C5-, C6-, and C7-nitroindoles

Sun, Li-Ping,Huang, Xiang-Hong,Dai, Wei Min

, p. 10983 - 10992 (2007/10/03)

A general and efficient synthesis of 2-substituted C5-, C6-, and C7-nitroindoles has been established. Starting from commercially available 2-amino nitrophenols, C5-, C6-, and C7-nitroindoles were synthesized via the stepwise Pd-catalyzed cross-coupling o

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