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4-HYDROXY-3-(TRIFLUOROMETHOXY)BENZALDEHYDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53104-95-3

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53104-95-3 Usage

Uses

4-Hydroxy-3-(trifluoromethoxy)benzaldehyde is a fluorinated compound, which is used for biochemical research.

Check Digit Verification of cas no

The CAS Registry Mumber 53104-95-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,1,0 and 4 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 53104-95:
(7*5)+(6*3)+(5*1)+(4*0)+(3*4)+(2*9)+(1*5)=93
93 % 10 = 3
So 53104-95-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H5F3O3/c9-8(10,11)14-7-3-5(4-12)1-2-6(7)13/h1-4,13H

53104-95-3 Well-known Company Product Price

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  • Alfa Aesar

  • (H32602)  4-Hydroxy-3-(trifluoromethoxy)benzaldehyde, 98+%   

  • 53104-95-3

  • 250mg

  • 574.0CNY

  • Detail
  • Alfa Aesar

  • (H32602)  4-Hydroxy-3-(trifluoromethoxy)benzaldehyde, 98+%   

  • 53104-95-3

  • 1g

  • 1583.0CNY

  • Detail

53104-95-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Hydroxy-3-(trifluoromethoxy)benzaldehyde

1.2 Other means of identification

Product number -
Other names 4-HYDROXY-3-(TRIFLUOROMETHOXY)BENZALDEHYDE

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:53104-95-3 SDS

53104-95-3Relevant academic research and scientific papers

ISOINDOLINE COMPOSITIONS AND METHODS FOR TREATING NEURODEGENERATIVE DISEASE

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Paragraph 0447;0449, (2015/09/23)

Isoindoline sigma-2 receptor antagonist compounds, pharmaceutical compositions comprising such compounds, and methods for inhibiting Abeta- associated synapse loss or synaptic dysfunction in neuronal cells, modulating an Abeta-associated membrane trafficking change in neuronal cells, and treating cognitive decline associated with Abeta pathology are provided.

1 -HYDROXY-BENZOOXABOROLES AS ANTIPARASITIC AGENTS

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Page/Page column 111, (2014/10/03)

Provided are compounds useful for controlling endoparasites both in animals and agriculture. Further provided are methods for controlling endoparasite infestations of an animal by administering an effective amount of a compound as described above, or a pharmaceutically acceptable salt thereof, to an animal, as well as formulations for controlling endoparasite infestations using the compounds described above or an acceptable salt thereof, and an acceptable carrier. The claimed compounds are described by the following Markush formula:A typical example for a compound according to above formula is: A typical example for a compound according to above formula is:

Synthesis and fungicidal activity of new fluorine-containing mandelic acid amide compounds

Li, Shuai,Cui, Can,Wang, Man-Yi,Yu, Shui-Jing,Shi, Yan-Xia,Zhang, Xiao,Li, Zheng-Ming,Zhao, Wei-Guang,Li, Bao-Ju

experimental part, p. 108 - 112 (2012/06/15)

A series of novel fluorine-containing mandelic acid amide compounds were designed and synthesized by a facile method, and their structures were characterized by 1H nuclear magnetic resonance (NMR) and high-resolution mass spectrometry. The preliminary in vivo bioassays indicated that some of the title compounds showed excellent fungicidal activities in vivo against Pseudoperonospora cubensis at the dosage of 25 mg L-1, which were comparable with the control (Mandipropamid).

ARYLALKYL- AND CYCLOALKYLALKYL-PIPERAZINE DERIVATIVES AND METHODS OF THEIR USE

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Page/Page column 223, (2008/06/13)

The present invention is directed to arylalkyl- and cycloalkylalkyl-piperazine derivatives, compositions containing these derivatives, and methods of their use for the prevention and treatment of conditions ameliorated by monoamine reuptake including, int

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