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1,4-Naphthalenediol, 6-chloro-2,3-dimethoxy-, dibenzoate is a complex organic compound with the chemical formula C24H18ClO5. It is derived from 1,4-naphthoquinone, a type of quinone, and features a naphthalene ring structure with a hydroxyl group at the 1 and 4 positions, a chloro substituent at the 6 position, and two methoxy groups at the 2 and 3 positions. The dibenzoate refers to the esterification of the two hydroxyl groups with benzoic acid, resulting in a molecule with two benzoate ester groups. 1,4-Naphthalenediol, 6-chloro-2,3-dimethoxy-, dibenzoate is known for its potential applications in the synthesis of various pharmaceuticals and chemical intermediates, particularly in the area of organic synthesis. It is important to note that due to its complex structure and potential reactivity, it should be handled with care, following proper safety protocols.

97988-22-2

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97988-22-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97988-22-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,9,8 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 97988-22:
(7*9)+(6*7)+(5*9)+(4*8)+(3*8)+(2*2)+(1*2)=212
212 % 10 = 2
So 97988-22-2 is a valid CAS Registry Number.

97988-22-2Downstream Products

97988-22-2Relevant academic research and scientific papers

Topical Nonsteroidal Antipsoriatic Agents. 1. 1,2,3,4-Tetraoxygenated Naphthalene Derivatives

Jones, Gordon H.,Venuti, Michael C.,Young, John M.,Murthy, D.V. Krishna,Loe, Brad E.,et al.

, p. 1504 - 1511 (2007/10/02)

On the basis of previous observations that both 2,3-dihydro-2,2,3,3-tetrahydroxy-1,4-naphthoquinone (oxoline, 1) and 6-chloroisonaphthazarin (2) had demonstrated antipsoriatic activity in vivo, a series of structural derivatives of 2 were prepared and examined in the Scholtz-Dumas topical psoriasis bioassay.Of these six (5, 6, 9a, 10, 11a, 11b), the most effective compound was found to be 6-chloro-1,4-diacetoxy-2,3-dimethoxynaphthalene (RS-43179,lonapalene, 11a).An extensive series of 1,2,3,4-tetraoxygenated naphthalenes (16-74) incorporating variations of the ester, eth er and aryl substituents were prepared as analogues of 11a to examine the structural requirements for activity and were screened in vivo as inhibitors of arachidonic acid induced mouse ear edema, a topical bioassay capable of detecting 5-lipoxygenase inhibitors.Net lipophilicity, hydrolytic stability, and ring substitution play significant roles in determining the observed in vivo activity.Lonapalene (11a) is currently in clinical development as a topical applied nonsteroidal antipsoriatic agent.

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