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288588-11-4

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288588-11-4 Usage

Chemical class

Beta amino alcohols

Structure

Pyrrole ring attached to a pentanol chain, with a beta amino group and two phenylmethyl groups

Stereochemistry

(βS)indicating the absolute configuration of the beta carbon atom

Potential applications

Medicinal chemistry, as beta amino alcohols exhibit biological activity and can serve as building blocks for the synthesis of pharmaceuticals and other biologically active molecules

Importance of pyrrole ring

May contribute to potential pharmacological properties

Need for further research

To explore the properties and potential applications of this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 288588-11-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,8,5,8 and 8 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 288588-11:
(8*2)+(7*8)+(6*8)+(5*5)+(4*8)+(3*8)+(2*1)+(1*1)=204
204 % 10 = 4
So 288588-11-4 is a valid CAS Registry Number.

288588-11-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-(dibenzylamino)-5-pyrrol-1-ylpentan-2-ol

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:288588-11-4 SDS

288588-11-4Relevant articles and documents

Synthesis of enantiopure 8-aminomethylindolizines from glutamine by stereoelectronically controlled cationic cyclization

Lehmann, Thomas,Gmeiner, Peter

, p. 1371 - 1378 (2007/10/03)

Starting from natural glutamine the synthesis of the 8- aminomethylindolizine (4b) was accomplished. The construction of the ring system was performed by employing a cationic 6-exo π-cyclization of an intermediate aziridinium salt. Transformation of the N,N-dibenzyl protected amine (4b) into the pharmacologically relevant target compound (11) is also described.

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