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Ethanone, 1-(2-amino-5-methoxy-3-methylphenyl)-2-chloro- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74798-63-3

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74798-63-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74798-63-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,7,9 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 74798-63:
(7*7)+(6*4)+(5*7)+(4*9)+(3*8)+(2*6)+(1*3)=183
183 % 10 = 3
So 74798-63-3 is a valid CAS Registry Number.

74798-63-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-amino-5-methoxy-3-methylphenyl)-2-chloroethanone

1.2 Other means of identification

Product number -
Other names -

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:74798-63-3 SDS

74798-63-3Downstream Products

74798-63-3Relevant academic research and scientific papers

An indole derivative and its application

-

Paragraph 0113-0119, (2022/01/12)

The present invention relates to an indole derivative shown in formula (I-1) and its use in the preparation of a drug for the prevention and / or treatment of indications associated with the S1P receptor disorders. Indole derivatives of the present invent

Studies on Several 7-Substituted N,N-Dimethyltryptamines

Glennon, R. A.,Schubert, E.,Jacyno, J. M.,Rosecrans, J. A.

, p. 1222 - 1226 (2007/10/02)

Several 7-substituted derivatives of N,N-dimethyltryptamine (DMT) were prepared and evaluated in the rat fundus serotonin receptor assay and in a behavioral (discriminative stimulus) assay in rats.Both 7-Me- and 5-Ome-7-Me-DMT possess a higher pA2, and 5,7-(OMe)2-DMT a lower pA2, than that of DMT itself.Like DMT, all three of these compounds produce behavioral effects in rats which are similar to those of the hallucinogen 5-OMe-DMT.Although 7-Et- and 7-Br-DMT possess a higher serotonin receptor affinity than DMT, neither produce behavioral effects which parallelthose of 5-OMe-DMT.In contrast, 6-OMe-DMT and its 5-OMe derivative do not interact with the serotonin receptors in a competitive manner and are inactive in the discriminative stimulus assay.

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