86111-24-2 Usage
Molecular structure
1H-Indol-6-ol, 2-[3-(acetyloxy)phenyl]-1-ethyl-, acetate (ester) consists of a benzene ring fused to a five-membered nitrogen-containing ring, with an acetyloxy group attached to a phenyl group and an ethyl group attached to the indol-6-ol core.
Functional groups
The compound contains an acetyloxy group (OAc), a phenyl group (C6H5), and an ethyl group (C2H5).
Chemical classification
It is an indol-6-ol derivative, which is a type of organic compound with a benzene ring fused to a nitrogen-containing ring.
Ester functional group
The compound is an acetate ester, which means it contains an acetyl functional group (CH3COO) bonded to an oxygen atom.
Potential applications
1H-Indol-6-ol, 2-[3-(acetyloxy)phenyl]-1-ethyl-, acetate (ester) has potential applications in the pharmaceutical industry due to its indol-6-ol derivative nature.
Biological activities
Indol-6-ol derivatives, including 1H-Indol-6-ol, 2-[3-(acetyloxy)phenyl]-1-ethyl-, acetate (ester), have been studied for their potential biological activities, such as anti-inflammatory and anticancer effects.
Therapeutic potential
Further research is needed to fully understand the therapeutic potential of 1H-Indol-6-ol, 2-[3-(acetyloxy)phenyl]-1-ethyl-, acetate (ester) and other indol-6-ol derivatives.
Check Digit Verification of cas no
The CAS Registry Mumber 86111-24-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,1,1 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 86111-24:
(7*8)+(6*6)+(5*1)+(4*1)+(3*1)+(2*2)+(1*4)=112
112 % 10 = 2
So 86111-24-2 is a valid CAS Registry Number.
86111-24-2Relevant academic research and scientific papers
2-Phenylindoles. Relationship between Structure, Estrogen Receptor Affinity, and Mammary Tumor Inhibiting Activity in the Rat
Angerer, Erwin von,Prekajac, Jelica,Strohmeier, Josef
, p. 1439 - 1447 (2007/10/02)
A number of 2-phenylindole derivatives with one hydroxy group in the meta or para position of the phenyl ring and a second one in position 5, 6, or 7 of the indole nucleus were synthesized.In addition, different alkyl groups were introduced into positions
