87142-62-9 Usage
Explanation
The compound consists of 11 carbon atoms, 15 hydrogen atoms, 1 nitrogen atom, 1 oxygen atom, and 1 bromine atom.
Explanation
The compound contains a phenyl group (a six-carbon ring with alternating single and double bonds) with a chlorine atom attached to it.
Explanation
The compound has a dimethylamino group (two methyl groups attached to a nitrogen atom) as part of its structure.
Explanation
The presence of the hydrobromide salt (a bromide ion combined with a proton) indicates that the compound can form ionic interactions with other molecules.
Explanation
The compound is commonly used in the synthesis of pharmaceutical drugs, making it a valuable reagent in the development of new medications.
Explanation
Due to its chemical properties and reactivity, the compound has potential applications in the field of medicine, possibly contributing to the development of new therapeutic treatments.
Explanation
The presence of the hydrobromide salt allows the compound to form ionic interactions with other molecules, which can be useful in various research and industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 87142-62-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,1,4 and 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 87142-62:
(7*8)+(6*7)+(5*1)+(4*4)+(3*2)+(2*6)+(1*2)=139
139 % 10 = 9
So 87142-62-9 is a valid CAS Registry Number.
87142-62-9Relevant academic research and scientific papers
Evaluation of some Mannich bases derived from substituted acetophenones against P-388 lymphocytic leukemia and on respiration in isolated rat liver mitochondria
Dimmock,Shyam,Hamon,Logan,Raghavan,Harwood,Smith
, p. 887 - 894 (2007/10/02)
Series of 3-dimethylamino-1-aryl-1-propanone hydrobromides (IV) and 3-dimethylamino-2-dimethylaminomethyl-1-aryl-1-propanone dihydrobromides (V) were synthesized. Evaluation of these derivatives against P-388 lymphocytic leukemia growth revealed that two compounds show promise as antineoplastic agents. Compounds of the V series were unstable in phosphate buffer (in contrast to series IV), and when the same nuclear substituent was present in both series of compounds, V was ~ 100 times more active than IV in both the stimulation and inhibition of respiration of mitochondria isolated from rat liver cells. Representatives from both series showed that respiration in mitochondria was affected by changing the pH of the aqueous buffer from 7.4 to 6.9 or 6.4 and by reducing the temperature from 37° to 20°. The compounds showed reactivity toward a biomimetic thiol.
