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1H-Indol-6-ol, 2-(4-hydroxyphenyl)-3-methyl-1-(1-methylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91444-56-3

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91444-56-3 Usage

Compound type

Derivative of indole, a heterocyclic compound.

Hydroxyphenyl group

A phenyl ring with a hydroxyl group (-OH).

Methyl-isopropyl group

A -CH3 group attached to an isopropyl group (-CH(CH3)2).

Antioxidant

Capable of neutralizing free radicals, thus preventing oxidative damage to cells.

Anti-inflammatory

Reduces inflammation in the body, which can be beneficial in treating various diseases.

Cancer treatment

May help in inhibiting cancer cell growth and proliferation.

Diabetes treatment

May help in regulating blood sugar levels and improving insulin sensitivity.

Neurodegenerative disorders

May help in slowing down the progression of diseases such as Alzheimer's and Parkinson's.

Other potential roles

Regulating hormone levels and cell signaling pathways.

Check Digit Verification of cas no

The CAS Registry Mumber 91444-56-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,4,4 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 91444-56:
(7*9)+(6*1)+(5*4)+(4*4)+(3*4)+(2*5)+(1*6)=133
133 % 10 = 3
So 91444-56-3 is a valid CAS Registry Number.

91444-56-3Relevant 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

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