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About This Item
Linear Formula:
(CH3)3COCONHCH2CH2NH2
CAS Number:
Molecular Weight:
160.21
UNSPSC Code:
12352116
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1932330
Assay:
≥98.0% (NT)
InChI
1S/C7H16N2O2/c1-7(2,3)11-6(10)9-5-4-8/h4-5,8H2,1-3H3,(H,9,10)
SMILES string
NCCNC(OC(C)(C)C)=O
InChI key
AOCSUUGBCMTKJH-UHFFFAOYSA-N
assay
≥98.0% (NT)
reaction suitability
reagent type: cross-linking reagent
Quality Level
refractive index
n20/D 1.458
bp
72-80 °C/0.1 mmHg (lit.)
density
1.012 g/mL at 20 °C (lit.)
functional group
Boc, amine
Application
- Facile synthesis of new N-(aminocycloalkylene) amino acid compounds: Describes the use of N-Boc-ethylenediamine in the preparation of benzyl 2-{[2-(Boc-amino)ethyl]amino}acetate (G Matulevičiūtė et al., 2023).
- Synthesis of a new tripod BODIPY dye: Reports on the chemical synthesis involving N-Boc-ethylenediamine for creating a BODIPY dye (H Wang et al., 2022).
- Single‐Entity Electrocatalysis: Discusses the application of N-Boc-ethylenediamine in modifying Co3O4 nanoparticles used in electrocatalysis (T Quast et al., 2021).
Other Notes
Mono-protected derivative of ethylenediamine, preparation of pharmacologically active analogues; introduction of an ethylenediamine spacer.
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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Deborah Sultan et al.
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Russell D Viirre et al.
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An improved synthesis of ethyl N-[(2-Boc-amino)ethyl]glycinate and its hydrochloride salt is reported. The synthesis is based on the reductive alkylation of Boc-ethylenediamine with ethyl glyoxylate hydrate and furnishes the title compound in near quantitative yield and high purity without chromatography.
E Morier-Teissier et al.
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M M Dowd et al.
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Intravitreal injection of antiangiogenic agents is becoming a standard treatment for neovascular retinal diseases. Sustained release of therapeutics by injecting colloidal carriers is a promising approach to reduce the injection frequency, which reduces treatment burdens and the risk of complications
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