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191864-24-1

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  • ethyl 3-[2-(dimethylamino)ethyl]-5-[[(4S)-2-oxo-1,3-oxazolidin-4-yl]methyl]-1H-indole-2-carboxylate

    Cas No: 191864-24-1

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191864-24-1 Usage

Uses

Different sources of media describe the Uses of 191864-24-1 differently. You can refer to the following data:
1. (S)-3-[2-(Dimethylamino)ethyl]-5-[[(4S)-2-oxo-4-oxazolidinyl]methyl]-1H-indole-2-carboxylic Acid Ethyl Ester, is a derivative of Zolmitriptan (Z639000), a Serotonin 5HTID-receptor agonist.
2. (S)-3-[2-(Dimethylamino)ethyl]-5-[[(4S)-2-oxo-4-oxazolidinyl]methyl]-1H-indole-2-carboxylic Acid Ethyl Ester (Zolmitriptan USP Related Compound D), is a derivative of Zolmitriptan (Z639000), a Serotonin 5HTID-receptor agonist.

Check Digit Verification of cas no

The CAS Registry Mumber 191864-24-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,8,6 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 191864-24:
(8*1)+(7*9)+(6*1)+(5*8)+(4*6)+(3*4)+(2*2)+(1*4)=161
161 % 10 = 1
So 191864-24-1 is a valid CAS Registry Number.

191864-24-1 Well-known Company Product Price

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  • USP

  • (1727053)  Zolmitriptan Related Compound D  United States Pharmacopeia (USP) Reference Standard

  • 191864-24-1

  • 1727053-20MG

  • 14,500.98CNY

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191864-24-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-[2-(dimethylamino)ethyl]-5-[[(4S)-2-oxo-1,3-oxazolidin-4-yl]methyl]-1H-indole-2-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 3-(2-dimethylaminoethyl)-5-[(4S)-2-oxooxazolidin-4-ylmethyl]-1H-indole-2-carboxylate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:191864-24-1 SDS

191864-24-1Downstream Products

191864-24-1Relevant articles and documents

Synthesis of zolmitriptan and related substances

Vujjini, Satish Kumar,Mothukuri, Vivekananda Reddy,Islam, Aminul,Bandichhor, Rakeshwar,Kagga, Mukkanti,Malakondaiah, Golla China

, p. 3294 - 3306 (2013/10/01)

Efficient and cost-effective synthesis of Zolmitriptan 1 employing Japp-Klingemann reaction and a new robust purification strategy is described.

PROCESS FOR PREPARING ZOLMITRIPTAN COMPOUNDS

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Page 16-17, (2008/06/13)

In particular, zolmitriptan or a pharmaceutically acceptable salt thereof, which includes a) Preparation of the diazonium salt of the aniline hydrochloride (II); followed by reduction and acidification to give hydrazine (III); b) In situ Reaction of the hydrazine hydrochloride (III) with ?-keto-?-valerolactone, to give the hydrazone (IV); c) Fischer indole synthesis of the hydrazone (IV), to give the pyranoindolone of formula (V); d) Transesterification of the pyranoindolone (V) to provide the compound (VI), in which R means a straight or branched C1-C4 alkyl; e) Conversion of the hydroxyl group of the compound (VI) into dimethylamino to give the indolecarboxylate (VII), in which R means a straight or branched C1-C4 alkyl; f) Saponification of the 2-carboalkoxy group of the compound (VII), to provide indolecarboxylic acid (VIII); g) Decarboxylation of the indolecarboxylic acid (VIII), to provide zolmitriptan and, eventually, to provide a pharmaceutically acceptable salt thereof.

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