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56935-71-8

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56935-71-8 Usage

Description

4-(Trifluoromethoxy)benzamidoxime (4-TFMBAO) is a benzamidoxime (BAO) derivative that contains an amidoxime functional group. It is characterized by its white crystalline appearance and has been studied for its density and freezing point properties.

Uses

Used in Analytical Chemistry:
4-(Trifluoromethoxy)benzamidoxime is used as an analyte in the selective, sensitive, and fluorometric detection of urinary cytosine. This application is significant for the analysis and monitoring of various biological processes and conditions.
Used in Fluorescence Deriving Reactions:
4-(Trifluoromethoxy)benzamidoxime (4-TFMBAO) is a suitable reactant in the fluorescence (FL) deriving reaction, a widely-used methodology specifically designed to quantify uracil. This makes it a valuable tool in research and diagnostics related to nucleic acid analysis.
Used in Synthesis of Oxadiazoles:
4-(Trifluoromethoxy)benzamidoxime may be used as a reactant in the synthesis of oxadiazoles, which are important compounds in various fields, including pharmaceuticals and materials science.
Used in Quantification of Orotic Acid:
4-(Trifluoromethoxy)benzamidoxime may also be used as a fluorogenic agent in the quantification of orotic acid by spectrofluorometric methods in human biological specimens. This application is crucial for understanding and diagnosing metabolic disorders related to orotic acid metabolism.

Check Digit Verification of cas no

The CAS Registry Mumber 56935-71-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,9,3 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 56935-71:
(7*5)+(6*6)+(5*9)+(4*3)+(3*5)+(2*7)+(1*1)=158
158 % 10 = 8
So 56935-71-8 is a valid CAS Registry Number.

56935-71-8 Well-known Company Product Price

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  • Aldrich

  • (422231)  4-(Trifluoromethoxy)benzamidoxime  97%

  • 56935-71-8

  • 422231-1G

  • 761.67CNY

  • Detail

56935-71-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(TRIFLUOROMETHOXY)BENZAMIDOXIME

1.2 Other means of identification

Product number -
Other names N'-hydroxy-4-(trifluoromethoxy)benzeneamidine

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:56935-71-8 SDS

56935-71-8Downstream Products

56935-71-8Relevant articles and documents

MOLECULES HAVING CERTAIN PESTICIDAL UTILITIES, AND INTERMEDIATES, COMPOSITIONS, AND PROCESSES RELATED THERETO

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Page/Page column 329, (2021/02/12)

This disclosure relates to compounds having pesticidal utility against pests in phyla Nematoda, Arthropoda, and/or Mollusca, processes to produce such compounds and intermediates used in such processes, compositions containing such compounds, and processes of using such compounds against such pests. These compounds/molecules may be used, for example, as nematicides, acaricides, insecticides, miticides, and/or molluscicides. This document discloses compounds having the following formula (Formula One and/or Formula One-A).

KCNT1 INHIBITORS AND METHODS OF USE

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Paragraph 000462, (2020/11/23)

The present invention is directed to, in part, compounds and compositions useful for preventing and/or treating a neurological disease or disorder, a disease or condition relating to excessive neuronal excitability, and/or a gain-of-function mutation in a gene (e.g., KCNT1). Methods of treating a neurological disease or disorder, a disease or condition relating to excessive neuronal excitability, and/or a gain-of-function mutation in a gene such as KCNT1 are also provided herein.

Indazole-oxadiazole derivative, medicinal composition containing derivative, and application of derivative in tumor prevention

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Paragraph 0099; 0100, (2017/07/25)

The invention discloses an indazole-oxadiazole derivative with the structure represented by general formula a shown in the description, or a pharmaceutically acceptable salt or solvate thereof. In the formula, X is O or N, Y is N, Z is N or O, and all groups are as defined in the description. The invention also discloses a medicinal composition adopting the derivative as an active component, and a use of the derivative. Compounds synthesized in the invention have an HIF-1 inhibition effect, and most of the compounds have a substantial HIF-1 inhibition effect, have strong in-vivo and in-vitro anti-HIF-1 effect on human colorectal carcinoma cell strains (HCT116) and other tumor cell strains, and can be used for treating tumor diseases.

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