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188397-05-9

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188397-05-9 Usage

Chemical Properties

6-Acetyl-3-[2-(acetylaMino)ethyl]-5-Methoxy-H-indole-1-carboxylic Acid Ethyl Ester is Yellow Solid

Uses

6-Acetyl-3-[2-(acetylaMino)ethyl]-5-Methoxy-H-indole-1-carboxylic Acid Ethyl Ester is used in the preparation of 6-hydroxymelatonin (H944625), a human metabolite of melatonin (M215000).

Check Digit Verification of cas no

The CAS Registry Mumber 188397-05-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,3,9 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 188397-05:
(8*1)+(7*8)+(6*8)+(5*3)+(4*9)+(3*7)+(2*0)+(1*5)=189
189 % 10 = 9
So 188397-05-9 is a valid CAS Registry Number.

188397-05-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-(2-acetamidoethyl)-6-acetyl-5-methoxyindole-1-carboxylate

1.2 Other means of identification

Product number -
Other names 6-Acetyl-N-caboxylate Melatonin Ethyl Ester

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:188397-05-9 SDS

188397-05-9Relevant articles and documents

An efficient synthesis of 6-hydroxymelatonin, a human metabolite of melatonin

Karam, Omar,Zunino, Fabien,Chagnaut, Vincent,Jouannetaud, Marie Paule,Jacquesy, Jean Claude

, p. 1511 - 1513 (2007/10/03)

A four-step synthesis of 6-hydroxymelatonin 5, major human metabolite of melatonin 1, is reported starting from melatonin. The synthesis involves in the keys steps a regioselective Friedel-Crafts acylation followed by a Baeyer-Villiger oxidation. The overall yield is 48%.

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