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98799-37-2

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98799-37-2 Usage

General Description

1-(4-isopropoxy-3-methoxyphenyl)methanamine, also known as 4-Isopropoxy-3-methoxyphenyl)methanamine or IPMP, is a chemical compound with a molecular formula C11H17NO2. It belongs to the class of phenethylamine derivatives and is commonly used in the synthesis of pharmaceuticals, particularly as a precursor for the production of various psychoactive substances. IPMP is a potent and selective serotonin 5-HT2A receptor agonist, which makes it useful in the development of drugs for treating psychiatric disorders and neurological conditions. It also has potential applications in research and development of new medical treatments. However, due to its psychoactive properties, it is regulated and controlled in many countries.

Check Digit Verification of cas no

The CAS Registry Mumber 98799-37-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,7,9 and 9 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 98799-37:
(7*9)+(6*8)+(5*7)+(4*9)+(3*9)+(2*3)+(1*7)=222
222 % 10 = 2
So 98799-37-2 is a valid CAS Registry Number.

98799-37-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-methoxy-4-propan-2-yloxyphenyl)methanamine,hydrochloride

1.2 Other means of identification

Product number -
Other names 3-methoxy-4-isopropoxybenzylamine

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:98799-37-2 SDS

98799-37-2Relevant articles and documents

Synthesis and topoisomerase i inhibitory activity of a novel diazaindeno[2,1-b]phenanthrene analogue of Lamellarin D

Cananzi, Salvatore,Merlini, Lucio,Artali, Roberto,Beretta, Giovanni Luca,Zaffaroni, Nadia,Dallavalle, Sabrina

experimental part, p. 4971 - 4984 (2011/10/05)

A novel 5-oxa-6a,8-diazaindeno[2,1-b]phenanthren-7-one scaffold was designed and synthesized as an active analogue of the cytotoxic marine alkaloid Lamellarin D. The design was based on molecular modeling of the site of interaction of Lamellarin D with DNA-topoisomerase I cleavable complex, whereas the synthesis capitalized on a simple Friedel-Crafts cyclization of indole to a β-carbolinone nucleus. The product exhibited topoisomerase I poisoning activity and submicromolar cytotoxicity on human non-small cell lung cancer H460 cell line.

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