87497-32-3 Usage
Molecular Weight
369.53 g/mol
Functional Groups
Two dimethylamino groups (-N(CH3)2)
Phenylprop-2-en-1-ylidene group (C6H5-CH=CH-CH-)
Two ketone groups (C=O)
Structural Features
Heptane backbone (C7H16)
2E configuration in the phenylprop-2-en-1-ylidene group
Potential Applications
Dye or pigment (due to dimethylamino groups)
Organic synthesis (due to heptane backbone and phenylprop-2-en-1-ylidene group)
Pharmaceutical intermediate (due to complex structure and potential reactivity)
Synthetic Molecule
Likely to be synthesized in a laboratory setting
Industrial Uses
Potential uses in chemical and pharmaceutical industries
Solubility
Likely soluble in organic solvents such as ethanol, methanol, or acetone
Stability
May be sensitive to light, heat, or moisture due to the presence of the phenylprop-2-en-1-ylidene group and dimethylamino groups
Reactivity
Could potentially react with nucleophiles, electrophiles, or other reactive species due to the presence of ketone and ylidene groups
Check Digit Verification of cas no
The CAS Registry Mumber 87497-32-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,4,9 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 87497-32:
(7*8)+(6*7)+(5*4)+(4*9)+(3*7)+(2*3)+(1*2)=183
183 % 10 = 3
So 87497-32-3 is a valid CAS Registry Number.
87497-32-3Relevant academic research and scientific papers
Antileukemic evaluation of some Mannich bases derived from 2-arylidene-1,3-diketones
Dimmock,Raghavan,Logan,Bigam
, p. 248 - 254 (2007/10/02)
The synthesis of a number of Mannich bases derived from some 3-phenylmethylene-2,4-pentanediones and 3-(3-phenyl-2-propenylidene)-2,4-pentanedione has been accomplished and the compounds were evaluated against P388 lymphocytic leukemia. Three of the thirt
