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1,4-Naphthalenediol, 2,3-dimethoxy-5-(phenylthio)-, diacetate is a complex organic compound with the chemical formula C20H18O6S. It is derived from 1,4-naphthoquinone, a type of quinone, and features two methoxy groups at the 2 and 3 positions, a phenylthio group at the 5 position, and two acetate groups. 1,4-Naphthalenediol, 2,3-dimethoxy-5-(phenylthio)-, diacetate is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds due to its unique structure and reactivity. It is typically used as an intermediate in chemical reactions, allowing for the creation of a variety of derivatives with different properties and functionalities. The compound's specific structure and reactivity make it a valuable tool in the field of organic chemistry, particularly in the development of new drugs and other chemical products.

91814-53-8

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91814-53-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91814-53-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,8,1 and 4 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 91814-53:
(7*9)+(6*1)+(5*8)+(4*1)+(3*4)+(2*5)+(1*3)=138
138 % 10 = 8
So 91814-53-8 is a valid CAS Registry Number.

91814-53-8Downstream Products

91814-53-8Relevant 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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