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1,4-Naphthoquinone-1,4-hydroquinone, also known as lawsone or henna, is a naturally occurring organic compound derived from the henna plant (Lawsonia inermis). It is a colorless crystalline substance that belongs to the class of quinones, specifically a dihydroxynaphthoquinone. 1,4-naphthoquinone-1,4-hydroquinone is widely used in the cosmetic and hair dye industry due to its ability to bind with proteins, such as keratin in hair, and impart a reddish-brown color. Additionally, it has been studied for its potential medicinal properties, including antimicrobial, antioxidant, and anti-inflammatory effects. The compound's chemical structure consists of a naphthalene ring with two hydroxyl groups at the 1 and 4 positions, making it a valuable component in various applications.

60706-28-7

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60706-28-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60706-28-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,7,0 and 6 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 60706-28:
(7*6)+(6*0)+(5*7)+(4*0)+(3*6)+(2*2)+(1*8)=107
107 % 10 = 7
So 60706-28-7 is a valid CAS Registry Number.

60706-28-7Downstream Products

60706-28-7Relevant academic research and scientific papers

SOLID-STATE FORMATION OF QUINHYDRONES FROM THEIR COMPONENTS. USE OF SOLID-SOLID REACTIONS TO PREPARE COMPOUNDS NOT ACCESSIBLE FROM SOLUTION.

Patil,Curtin,I. C. Paul

, p. 348 - 353 (2007/10/02)

Selective molecular mobility provided by working with crystalline solids has been employed to prepare unsymmetrically substituted quinhydrones too unstable with respect to self-oxidation-reduction to be prepared by crystallization from solution. Reaction is carried out by grinding the solid components together with a mortar and pestle. Examination of the products with differential scanning calorimetry, X-ray powder photography, and Fourier transform infrared spectroscopy shows that the complexation reaction goes to completion under conditions in which no detectible redox reaction has occurred. The products are shown by X-ray powder photography to be formed in a microcrystalline state.

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