116070-39-4 Usage
Uses
Used in Organic Synthesis:
3-Methyl-5-(trifluoromethyl)benzaldehyde is used as an intermediate in the synthesis of complex organic compounds. Its presence of a trifluoromethyl group and a methyl group attached to the benzene ring, along with the aldehyde group, makes it a valuable building block for creating a variety of molecules with potential applications in different industries.
Used in Pharmaceutical Industry:
3-Methyl-5-(trifluoromethyl)benzaldehyde is used as a key component in the development of new pharmaceutical compounds. Its unique structure allows for the creation of molecules with specific properties, such as increased stability or targeted activity, which can be beneficial in the design of new drugs.
Used in Chemical Research:
3-Methyl-5-(trifluoromethyl)benzaldehyde is used as a research tool in the study of chemical reactions and mechanisms. Its reactivity and the presence of the trifluoromethyl and methyl groups make it an interesting subject for investigating the effects of these functional groups on reaction pathways and outcomes.
Used in Material Science:
3-Methyl-5-(trifluoromethyl)benzaldehyde is used in the development of new materials with specific properties, such as improved thermal stability or enhanced chemical resistance. Its incorporation into polymers or other materials can lead to the creation of novel products with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 116070-39-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,0,7 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 116070-39:
(8*1)+(7*1)+(6*6)+(5*0)+(4*7)+(3*0)+(2*3)+(1*9)=94
94 % 10 = 4
So 116070-39-4 is a valid CAS Registry Number.
116070-39-4Relevant articles and documents
Piperidine derivative and use thereof
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Page/Page column 79-80, (2008/06/13)
The present invention provides a compound represented by the formula: wherein Ar is an aryl group optionally having substituents, R is a C1-6 alkyl group, R1 is a hydrogen atom, a hydrocarbon group optionally having substituents, an
5-amino or substituted amino 1,2,3-triazoles
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, (2008/06/13)
Novel 5-amino or substituted amino 1,2,3-triazoles are disclosed as having anticoccidial activity. The compounds are useful for controlling coccidiosis when administered in minor quantities to animals, in particular to poultry, usually in admixture with animal sustenance.
