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3,5-Bis(trifluoromethyl)benzamidoxime, also known as N′-hydroxy-3,5-bis(trifluoromethyl)benzenecarboximidamide, is a BAO (3,5-bis(trifluoromethyl)) derivative that features an amidoxime functional group. 3,5-BIS(TRIFLUOROMETHYL)BENZAMIDOXIME is characterized by the presence of two trifluoromethyl groups attached to a benzene ring, with an amidoxime group connected to the nitrogen atom.

72111-09-2

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72111-09-2 Usage

Uses

Used in Chemical Synthesis:
3,5-Bis(trifluoromethyl)benzamidoxime is used as a key intermediate in the synthesis of various organic compounds and pharmaceuticals. Its unique structure and functional groups make it a versatile building block for creating a wide range of molecules with potential applications in different industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3,5-Bis(trifluoromethyl)benzamidoxime is used as a precursor for the development of new drugs. Its amidoxime group can be utilized to form various bioactive molecules with potential therapeutic properties. The trifluoromethyl groups also contribute to the compound's lipophilicity, which can enhance its pharmacokinetic properties and improve its ability to cross biological barriers.
Used in Agrochemical Industry:
3,5-Bis(trifluoromethyl)benzamidoxime can be employed as a starting material for the synthesis of agrochemicals, such as pesticides and herbicides. Its structural features and functional groups can be modified to create compounds with specific target pest or weed control properties, contributing to more effective and selective crop protection solutions.
Used in Material Science:
In the field of material science, 3,5-Bis(trifluoromethyl)benzamidoxime can be used to develop novel materials with unique properties. Its amidoxime group can participate in coordination with metal ions, making it a potential candidate for the creation of metal-organic frameworks (MOFs) or other coordination polymers with applications in catalysis, gas storage, or sensing.
Overall, 3,5-Bis(trifluoromethyl)benzamidoxime is a versatile compound with a wide range of potential applications across various industries, including chemical synthesis, pharmaceuticals, agrochemicals, and material science. Its unique structure and functional groups make it a valuable building block for the development of new molecules and materials with diverse properties and uses.

Check Digit Verification of cas no

The CAS Registry Mumber 72111-09-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,1,1 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 72111-09:
(7*7)+(6*2)+(5*1)+(4*1)+(3*1)+(2*0)+(1*9)=82
82 % 10 = 2
So 72111-09-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H6F6N2O/c10-8(11,12)5-1-4(7(16)17-18)2-6(3-5)9(13,14)15/h1-3,18H,(H2,16,17)

72111-09-2 Well-known Company Product Price

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  • Aldrich

  • (542830)  3,5-Bis(trifluoromethyl)benzamidoxime  97%

  • 72111-09-2

  • 542830-1G

  • 940.68CNY

  • Detail

72111-09-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N'-Hydroxy-3,5-bis(trifluoromethyl)benzimidamide

1.2 Other means of identification

Product number -
Other names 3,5-BIS(TRIFLUOROMETHYL)BENZAMIDOXIME

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:72111-09-2 SDS

72111-09-2Relevant academic research and scientific papers

Pharmacophore requirements for HIV-1 reverse transcriptase inhibitors that selectively “Freeze” the pre-translocated complex during the polymerization catalytic cycle

Lacbay, Cyrus M.,Menni, Michael,Bernatchez, Jean A.,G?tte, Matthias,Tsantrizos, Youla S.

, p. 1713 - 1726 (2018/02/27)

Reverse transcriptase (RT) is responsible for replicating the HIV-1 genome and is a validated therapeutic target for the treatment of HIV infections. During each cycle of the RT-catalyzed DNA polymerization process, inorganic pyrophosphate is released as the by-product of nucleotide incorporation. Small molecules were identified that act as bioisosteres of pyrophosphate and can selectively freeze the catalytic cycle of HIV-1 RT at the pre-translocated stage of the DNA- or RNA-template-primer-enzyme complex.

Synthesis and fungicidal activities of novel bis(trifluoromethyl)phenyl- based strobilurins

Liu, Aiping,Wang, Xiaoguang,Ou, Xiaoming,Huang, Mingzhi,Chen, Can,Liu, Shudong,Huang, Lu,Liu, Xinping,Zhang, Chenglai,Zheng, Yongquan,Ren, Yeguo,He, Lian,Yao, Jianren

scheme or table, p. 6562 - 6566 (2010/04/06)

Strobilurins have become one of the most important classes of agricultural fungicides. To search for novel strobilurin compounds with unique biological activities, novel bis(trifluoromethyl)phenyl-based strobilurin analogues were synthesized by the reacti

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