| Identification | Back Directory | [Name]
N-TERT-BUTOXYCARBONYL-AZIDO-D-ALANINE | [CAS]
225780-77-8 | [Synonyms]
Boc-D-Aza-OH
Boc-D-Dap(N3)-OH
Boc-D-Aza-OH*CHA
Boc-D-Ala(N3)·CHA
Boc-D-Dap(N3)-OH·CHA
Boc-D-Dap(N3) CHA salt
3-Azido-N-Boc-D-alanine
N-TERT-BUTOXYCARBONYL-AZIDO-D-ALANINE
Boc-D-Dap(N3) CHA salt,3-Azido-N-Boc-D-alanine
3-Azido-N-[(1,1-dimethylethoxy)carbonyl]-D-alanine
2-(R)-(tert-butoxycarbonyl)-amino-3-azidopropionic acid
Nα-Boc-Nβ-Azido-D-2,3-diaminopropionic acid cyclohexylammonium salt≥ 99% (HPLC) | [Molecular Formula]
C8H14N4O4 | [MDL Number]
MFCD18252752 | [MOL File]
225780-77-8.mol | [Molecular Weight]
230.22 |
| Hazard Information | Back Directory | [Chemical Properties]
White crystalline powder | [Uses]
Boc-D-Aza-OH is a click chemistry reagent containing an azide group. Click chemistry has great potential for use in binding between nucleic acids, lipids, proteins, and other molecules, and has been used in many research fields because of its beneficial characteristics, including high yield, high specificity, and simplicity[1]. It contains an azide group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing alkyne groups. It can also undergo ring strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing DBCO or BCN groups. | [References]
[1] Jiang X, et al. Recent applications of click chemistry in drug discovery. Expert Opin Drug Discov. 2019 Aug;14(8):779-789. DOI:10.1080/17460441.2019.1614910 |
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| Company Name: |
Alabiotech Inc.
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| Tel: |
001-619-354-5251 |
| Website: |
www.alabiotech-e.com |
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