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288588-10-3

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288588-10-3 Usage

General Description

1-Pentanol, 5-aMino-2-[bis(phenylMethyl)aMino]-, (2S)- is a chemical compound with the molecular formula C21H29N3O. It is a chiral amine with a pentanol group and two phenylmethylamino groups. 1-Pentanol, 5-aMino-2-[bis(phenylMethyl)aMino]-, (2S)- is used in organic chemistry and pharmaceutical research as a building block for the synthesis of various compounds. It may also have potential applications in the field of medicine and drug development due to its structural features and potential biological activity. Further research and testing may be needed to fully understand the properties and potential uses of this chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 288588-10-3 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 0 respectively.
Calculate Digit Verification of CAS Registry Number 288588-10:
(8*2)+(7*8)+(6*8)+(5*5)+(4*8)+(3*8)+(2*1)+(1*0)=203
203 % 10 = 3
So 288588-10-3 is a valid CAS Registry Number.

288588-10-3SDS

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)-5-amino-2-(dibenzylamino)pentan-1-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:288588-10-3 SDS

288588-10-3Relevant 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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