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191864-24-1

191864-24-1 structure

191864-24-1 structure

Name: ethyl 3-[2-(dimethylamino)ethyl]-5-[[(4S)-2-oxo-1,3-oxazolidin-4-yl]methyl]-1H-indole-2-carboxylate
Chemical Name: ethyl 3-[2-(dimethylamino)ethyl]-5-[[(4S)-2-oxo-1,3-oxazolidin-4-yl]methyl]-1H-indole-2-carboxylate
CAS Number: 191864-24-1
Molecular Formula: C₁₉H₂₅N₃O₄
Molecular Weight: 359.42000
Create Date: 2016-11-16 22:39:24
Modify Date: 2025-08-30 10:48:05

Name	ethyl 3-[2-(dimethylamino)ethyl]-5-[[(4S)-2-oxo-1,3-oxazolidin-4-yl]methyl]-1H-indole-2-carboxylate
Synonyms	ethyl 3-(2-dimethylaminoethyl)-5-[(4S)-2-oxooxazolidin-4-ylmethyl]-1H-indole-2-carboxylate Zolmitriptan related compound D (S)-ethyl 3-[2-(dimethylamino)ethyl]-5-[(2-oxo-1,3-oxazolidin-4-yl)methyl]-1H-indole-2-carboxylate 1H-Indole-2-carboxylic acid,3-(2-(dimethylamino)ethyl)-5-(((4S)-2-oxo-4-oxazolidinyl)methyl)-,ethyl ester Zolmitriptan 2-carboxylic acid ethyl ester ethyl 3-(2-dimethylaminoethyl)-5-[(4S)-2-oxo-1,3-oxazolan-4yl-methyl]-1H-2-indole carboxylate (S)-Ethyl 3-[2-(dimethylamino)ethyl]-5-[(2-oxooxazolidin-4-yl)methyl]-1H-indole-2-carboxylate Zolmitriptan related compound D RS [USP] (S)-3-(2-dimethylaminoethyl)-5-[2-oxo-1,3-oxazolidin-4-ylmethyl]-1H-indol-2-carboxylic acid ethyl ester

Molecular Formula	C₁₉H₂₅N₃O₄
Molecular Weight	359.42000
Exact Mass	359.18500
PSA	87.15000
LogP	1.73960

RIDADR	NONH for all modes of transport

659738-68-8 structure

659738-68-8

124-40-3 structure

124-40-3

~89%

191864-24-1 structure

191864-24-1

Literature: LABORATORIOS VITA, S. A. Patent: WO2004/14901 A1, 2004 ; Location in patent: Page 16-17 ;

63-91-2 structure

63-91-2

~%

191864-24-1 structure

191864-24-1

Literature: Moloney, Gerard P.; Robertson, Alan D.; Martin, Graeme R.; MacLennan, Steven; Mathews, Neil; Dodsworth, Susan; Sang, Pang Yih; Knight, Cameron; Glen, Robert Journal of Medicinal Chemistry, 1997 , vol. 40, # 15 p. 2347 - 2362

949-99-5 structure

949-99-5

~%

191864-24-1 structure

191864-24-1

Literature: Moloney, Gerard P.; Robertson, Alan D.; Martin, Graeme R.; MacLennan, Steven; Mathews, Neil; Dodsworth, Susan; Sang, Pang Yih; Knight, Cameron; Glen, Robert Journal of Medicinal Chemistry, 1997 , vol. 40, # 15 p. 2347 - 2362

89288-22-2 structure

89288-22-2

~%

191864-24-1 structure

191864-24-1

Literature: Moloney, Gerard P.; Robertson, Alan D.; Martin, Graeme R.; MacLennan, Steven; Mathews, Neil; Dodsworth, Susan; Sang, Pang Yih; Knight, Cameron; Glen, Robert Journal of Medicinal Chemistry, 1997 , vol. 40, # 15 p. 2347 - 2362

17193-40-7 structure

17193-40-7

~%

191864-24-1 structure

191864-24-1

Literature: Moloney, Gerard P.; Robertson, Alan D.; Martin, Graeme R.; MacLennan, Steven; Mathews, Neil; Dodsworth, Susan; Sang, Pang Yih; Knight, Cameron; Glen, Robert Journal of Medicinal Chemistry, 1997 , vol. 40, # 15 p. 2347 - 2362

139264-55-4 structure

139264-55-4

~%

191864-24-1 structure

191864-24-1

Literature: Moloney, Gerard P.; Robertson, Alan D.; Martin, Graeme R.; MacLennan, Steven; Mathews, Neil; Dodsworth, Susan; Sang, Pang Yih; Knight, Cameron; Glen, Robert Journal of Medicinal Chemistry, 1997 , vol. 40, # 15 p. 2347 - 2362

69472-61-3 structure

69472-61-3

~%

191864-24-1 structure

191864-24-1

Literature: Moloney, Gerard P.; Robertson, Alan D.; Martin, Graeme R.; MacLennan, Steven; Mathews, Neil; Dodsworth, Susan; Sang, Pang Yih; Knight, Cameron; Glen, Robert Journal of Medicinal Chemistry, 1997 , vol. 40, # 15 p. 2347 - 2362

5407-04-5 structure

5407-04-5

~%

191864-24-1 structure

191864-24-1

Literature: Moloney, Gerard P.; Robertson, Alan D.; Martin, Graeme R.; MacLennan, Steven; Mathews, Neil; Dodsworth, Susan; Sang, Pang Yih; Knight, Cameron; Glen, Robert Journal of Medicinal Chemistry, 1997 , vol. 40, # 15 p. 2347 - 2362

152305-23-2 structure

152305-23-2

~%

191864-24-1 structure

191864-24-1

Literature: Moloney, Gerard P.; Robertson, Alan D.; Martin, Graeme R.; MacLennan, Steven; Mathews, Neil; Dodsworth, Susan; Sang, Pang Yih; Knight, Cameron; Glen, Robert Journal of Medicinal Chemistry, 1997 , vol. 40, # 15 p. 2347 - 2362

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