1069085-41-1 Usage
Chemical class
Imidazole derivatives
A class of heterocyclic organic compounds with a wide range of biological activities.
Structure
Contains a phenyl group and a trifluoromethyl group
Phenyl group
Aromatic ring structure that contributes to the compound's stability and reactivity.
Trifluoromethyl group
A halogenated alkyl group that enhances chemical reactivity and stability.
Biological activities
Antifungal, antibacterial, and antiviral properties
These properties make the compound potentially useful in pharmaceutical and agrochemical industries.
Chemical reactivity
Influenced by the trifluoromethyl group
The presence of this group increases the compound's reactivity, which may be beneficial in various applications.
Stability
Enhanced by the trifluoromethyl group
The compound's stability is improved due to the presence of the trifluoromethyl group.
Potential applications
Pharmaceutical and agrochemical industries
The compound's biological activities and structural features make it a promising candidate for further research and development in these industries.
Need for further research
To explore potential uses and properties
More research and development are required to fully understand the compound's potential applications and properties.
Check Digit Verification of cas no
The CAS Registry Mumber 1069085-41-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,9,0,8 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1069085-41:
(9*1)+(8*0)+(7*6)+(6*9)+(5*0)+(4*8)+(3*5)+(2*4)+(1*1)=161
161 % 10 = 1
So 1069085-41-1 is a valid CAS Registry Number.
1069085-41-1Relevant articles and documents
A facile one-pot synthesis of 2-fluoroalkyl 1,3-imidazolines and 1,3-oxazolines through imidoyl halide intermediates
Jiang, Haizhen,Sun, Lan,Yuan, Shijie,Lu, Wenjun,Wan, Wen,Zhu, Shizheng,Hao, Jian
supporting information; experimental part, p. 2858 - 2863 (2012/05/05)
A facile one-pot procedure has been developed for the synthesis of 1,3-imidazolines and 1,3-oxazolines bearing fluorinated alkyl groups at the 2-position. The reaction involves the condensation of N-monosubstituted ethane-1,2-diamines or 2-aminoethanols with a fluorinated carboxylic acid in the presence of PPh3/CX4. The proposed mechanism is that the amide intermediates were initially formed, and then converted to the imidoyl halide intermediates in the presence of PPh3/CX4, followed by rapid intramolecular cyclization to 1,3-diazoline products. This protocol allows for the synthesis of 2-bromodifluoromethyl-1,3-imidazoline, a useful CF2Br-heterocyclic building block, which can be used for the synthesis of gem-difluoromethylene linked compounds.
