101571-08-8 Usage
Ketone functional group
This compound has a carbonyl group (C=O) attached to a two-carbon chain, classifying it as a ketone.
Bromine substitution
The compound has two bromine atoms attached to the third carbon of the ketone, which may influence its chemical reactivity and physical properties.
Halogenated compound
The presence of bromine and chlorine atoms makes this compound halogenated, which can affect its solubility, boiling point, and other physical properties.
Aromatic substitution
The compound has a 4-chlorophenyl group attached to the first carbon and a 4-(dimethylamino)phenyl group attached to the third carbon. These aromatic substituents may affect the compound's reactivity and stability.
Uncommon in nature
This compound is not commonly found in nature, indicating that it may have limited biological activity or environmental impact.
Synthetic compound
It is typically synthesized in a laboratory setting, which may limit its availability and use in practical applications.
Potential research and pharmaceutical applications
Due to its complex structure and unique chemical properties, this compound may be useful in research or in the development of new pharmaceuticals or other chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 101571-08-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,5,7 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 101571-08:
(8*1)+(7*0)+(6*1)+(5*5)+(4*7)+(3*1)+(2*0)+(1*8)=78
78 % 10 = 8
So 101571-08-8 is a valid CAS Registry Number.
101571-08-8Relevant articles and documents
Analgesic and antimicrobial studies of some 2,4-dichloro-5-fluorophenyl containing arylidenetriazolothiadiazines
Karthikeyan, Mari S.,Holla, Bantwal S.,Shenoy, Shalini
scheme or table, p. 707 - 716 (2009/07/25)
2,4-Dichloro-5-fluorophenyl containing 7-arylidenetriazolothiadiazines were obtained by the reaction of 4-amino-3-(2,4-dichloro-5-fluorophenyl)-5-mercapto- 1,2,4-triazole with 2,3-dibromo-1,3-diarylpropan-1-ones, and also by the reaction of 4-amino-3-(2,4
