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14453-65-7

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14453-65-7 Usage

General Description

1-(2-aminophenyl)pyrrolidin-2-one, also known as Prolintane, is a chemical compound with stimulant and nootropic properties. It is structurally related to pyrovalerone and inhibits the reuptake of norepinephrine and dopamine. Prolintane has been used as a performance-enhancing drug and an appetite suppressant, and has also been studied for its potential as a treatment for depression and cognitive impairment. However,

Check Digit Verification of cas no

The CAS Registry Mumber 14453-65-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,4,5 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 14453-65:
(7*1)+(6*4)+(5*4)+(4*5)+(3*3)+(2*6)+(1*5)=97
97 % 10 = 7
So 14453-65-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H12N2O/c11-8-4-1-2-5-9(8)12-7-3-6-10(12)13/h1-2,4-5H,3,6-7,11H2

14453-65-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-Aminophenyl)pyrrolidin-2-one

1.2 Other means of identification

Product number -
Other names 1-(2-amino-phenyl)-pyrrolidin-2-one

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:14453-65-7 SDS

14453-65-7Relevant articles and documents

Synthesis of annulated benzimidazoles via amidine cyclization

Liubchak, Kostiantyn,Nazarenko, Kostiantyn,Tolmachev, Andrey

scheme or table, p. 2993 - 3000 (2012/05/31)

Structurally diverse annulated benzimidazoles were synthesized via two copper(I)-catalyzed cyclocondensation reactions. In the first case the title compounds were prepared from lactams and o-bromoaniline. An alternative route consisted of an intramolecular cyclization of o-bromoarylamidines.

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