(S)-Benzyl 2-amino-6-((t-butoxycarbonyl)amino)hexanoate hydrochloride

Cat. No.: X24-09-YYX093

(S)-Benzyl 2-amino-6-((t-butoxycarbonyl)amino)hexanoate hydrochloride

Synonym: 133170-57-7; (S)-Benzyl 2-amino-6-((tert-butoxycarbonyl)amino)hexanoate hydrochloride; H-Lys(Boc)-OBzl.HCl; benzyl (2S)-2-amino-6-[(2-methylpropan-2-yl)oxycarbonylamino]hexanoate; Benzyl N6-(tert-butoxycarbonyl)-L-lysinate hydrochloride

  • CAS Number: 133170-57-7
  • PubChem CID: 92135159
Size
1 g; 5 g
Price
Datasheet
MSDS
Properties
Description
This compound is a chiral molecule with a benzyl group, amino and protected amino groups, and a hydrochloride salt. It is often used as an intermediate in the synthesis of pharmaceuticals and peptides. The protected amino groups allow for controlled chemical reactions during the synthesis process.
Molecular Weight
372.9
Molecular Formula
C18H29ClN2O4
Functional Group 1
Amine
Functional Group 2
Boc
Functional Group 3
None
Reactive Group 1
Acid
Form
Solid
Identity
Confirmed by NMR.
Applications
(S)-Benzyl 2-amino-6-((t-butoxycarbonyl)amino)hexanoate hydrochloride can be employed in the synthesis of peptides or as an intermediate in the production of certain pharmaceuticals.
Storage
Store at -20°C.
For Research Use Only. Not For Clinical Use.

Unleash the full potential of glycochemistry research with CD BioGlyco, the top CRO company committed to advancing the understanding of glycobiology through tailored solutions and exceptional expertise.

Copyright © CD BioGlyco. All Rights Reserved.
Top