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14471-17-1

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14471-17-1 Usage

General Description

N-(3,4,5-trimethoxybenzyl)cyclopropanamine is a chemical compound with the molecular formula C13H19NO3. It is a cyclopropanamine derivative with a benzyl group substituted with three methoxy groups at the 3, 4, and 5 positions. N-(3,4,5-trimethoxybenzyl)cyclopropanamine has been studied for its potential pharmacological properties, including its potential use as a psychoactive substance or in drug development. The specific biological activities and potential therapeutic applications of N-(3,4,5-trimethoxybenzyl)cyclopropanamine have not been fully elucidated, and further research is needed to fully understand its properties and potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 14471-17-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,4,7 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 14471-17:
(7*1)+(6*4)+(5*4)+(4*7)+(3*1)+(2*1)+(1*7)=91
91 % 10 = 1
So 14471-17-1 is a valid CAS Registry Number.

14471-17-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(3,4,5-trimethoxyphenyl)methyl]cyclopropanamine

1.2 Other means of identification

Product number -
Other names 3,4,5-Trimethoxybenzylcyclopropylamin = Cyclopropyl-(3,4,5-trimethoxy-benzyl)-amin

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:14471-17-1 SDS

14471-17-1Downstream Products

14471-17-1Relevant articles and documents

Synthesis of Colibactin Pyrrolidono[3,4- d]pyridones via Regioselective C(sp3)-H Activation

De Almeida Campos, Valery,Gademann, Karl,Huang, Bin,Ilazi, Agron

, p. 6858 - 6862 (2020)

The synthesis of pyrrolidono[3,4-d]pyridones of relevance to putative genotoxic colibactin structures featuring a doubly conjugated 1,6-Michael acceptor system is reported. We investigated and implemented a highly selective Pd-catalyzed C(sp3)-H activation reaction as a key step and further functionalized the pyridone core. Evaluating the role of this structural unit of relevance to colibactin, we found that this structure displayed a high degree of stability toward both acidic conditions and nucleophiles.

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