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13198-21-5

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13198-21-5 Usage

General Description

3-(Naphthalen-2-yl)propan-1-amine, also known as 2-(1-aminopropan-2-yl)naphthalene, is a chemical compound with the molecular formula C14H15N. It is an aromatic amine with a naphthalene group attached to a propan-1-amine moiety. 3-(NAPHTHALEN-2-YL)PROPAN-1-AMINE is primarily used as an intermediate in the production of pharmaceuticals, dyes, and other organic compounds. It has been studied for its potential bioactive properties, such as its ability to act as a serotonin reuptake inhibitor and its potential anticancer activity. Additionally, it has been investigated for its role as a building block in the synthesis of new organic molecules with potential industrial and medical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 13198-21-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,9 and 8 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13198-21:
(7*1)+(6*3)+(5*1)+(4*9)+(3*8)+(2*2)+(1*1)=95
95 % 10 = 5
So 13198-21-5 is a valid CAS Registry Number.

13198-21-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-naphthalen-2-ylpropan-1-amine

1.2 Other means of identification

Product number -
Other names 3-naphthalen-2-ylpropylamine

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:13198-21-5 SDS

13198-21-5Downstream Products

13198-21-5Relevant articles and documents

Synthesis of a novel tripeptidomimetic scaffold and biological evaluation for CXC chemokine receptor 4 (CXCR4) antagonism

Baumann, Markus,Nome, Lina Marie,Zachariassen, Zack G.,Karlsh?j, Stefanie,Fossen, Torgils,Rosenkilde, Mette M.,V?ben?, Jon,Haug, Bengt Erik

, p. 3866 - 3877 (2017/06/13)

We here report the preparation of a new 2,6,8-trisubstituted bicyclic tripeptidomimetic scaffold through TFA-mediated cyclization of a linear precursor containing three side chains. The introduction of a triphenylmethyl-protected thiol into carboxylic aci

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