N-Boc-ethylenediamine

CAS : 57260-73-8

Ref. 3D-FB18943

Informations sur le produit

• Nom: N-Boc-ethylenediamine
• Synonymes: tert-Butyl N-(2-aminoethyl)carbamateN-(2-Aminoethyl)carbamic acid 1,1-dimethylethyl ester(2-Aminoethyl)carbamic acid tert-butyl es terN-tert-Butoxycarbonylethylenediamine, (2-Aminoethyl)carbamic acid 1,1-dimethylethyl ester, (2-Aminoethyl)carbamic acid tert-butyl ester, 1,1-Dimethylethyl (2-aminoethyl)carbamate, 1-[(tert-Butoxycarbonyl)amino]-2-aminoethane, 2-(N-tert-Butoxycarbonylamino)ethylamine, 2-(tert-Butoxycarbonyl)amino-1-aminoethane, 2-[(tert-Butoxycarbonyl)amino]ethylamine, 2-[[(tert-Butyloxy)carbonyl]amino]ethylamine, Carbamic acid, (2-aminoethyl)-, 1,1-dimethylethyl ester, Carbamic acid, N-(2-aminoethyl)-, 1,1-dimethylethyl ester, N-(2-Aminoethyl)carbamic acid 1,1-dimethylethyl ester, N-(2-Aminoethyl)carbamic acid tert-butyl ester, N-(t-Butyloxycarbonyl)ethylenediamine, N-(tert-Butoxycarbonyl)-1,2-diaminoethane, N-(tert-Butoxycarbonyl)-1,2-ethanediamine, N-(tert-Butoxycarbonyl)ethylenediamine, N-BOC-1,2-Diaminoethane, N-Boc-1,2-ethylendiamine, N-Boc-Ethane-1,2-Diamine, N-Tert-Boc-Ethylenediamine, N-tert-Butoxycarbonyl-1,2-ethylenediamine, Tert-Butyl (2-Aminoethyl)Carbamate, Tert-Butyl 2-Aminoethylcarbamate, [(tert-Butyloxy)carbonyl]-1,2-ethylenediamine, mono-BOC-ethylenediamine, tert-Butyl N-(2-aminoethyl)carbamate, tert-Butyl [(2-aminoethyl)amino]formate
• CAS: 57260-73-8

Description

N-Boc-ethylenediamine is a chemical compound that belongs to the group of peptide hormones. It is historically used as a building block for peptides, such as luteinizing hormone releasing hormone (LHRH), which control reproduction and regulate the release of hormones. N-Boc-ethylenediamine has been shown to inhibit dpp-iv, an enzyme that breaks down proteins needed for cell growth and survival. This inhibition leads to cell death by apoptosis, or programmed cell death. N-Boc-ethylenediamine has also been shown to be an antimicrobial peptide against gram negative bacteria. The synthesis of this compound can be accomplished through several methods, including using diazonium salt or histone proteins. The analytical method involves hydrogen bonding between the amines and trifluoroacetic acid in order to produce the desired product.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 160.21 g/mol
• Formule: C₇H₁₆N₂O₂
• Degré de pureté: Min. 95%
• Couleur/Forme: Clear Liquid
• InChI: InChI=1S/C7H16N2O2/c1-7(2,3)11-6(10)9-5-4-8/h4-5,8H2,1-3H3,(H,9,10)
• Code InChI: InChIKey=AOCSUUGBCMTKJH-UHFFFAOYSA-N
• SMILES: CC(C)(C)OC(=O)NCCN