BENZYL N-(2-AMINOETHYL)CARBAMATE HYDROCHLORIDE
BENZYL N-(2-AMINOETHYL)CARBAMATE HYDROCHLORIDE Basic information
- Product Name:
- BENZYL N-(2-AMINOETHYL)CARBAMATE HYDROCHLORIDE
- Synonyms:
-
- BENZYL N-(2-AMINOETHYL)CARBAMATE HYDROCHLORIDE
- TIMTEC-BB SBB003280
- N-CBZ-1,2-DIAMINOETHANE HYDROCHLORIDE
- N-Z-ETHYLENEDIAMINE HYDROCHLORIDE
- N-Z-1,2-DIAMINOETHANE HYDROCHLORIDE
- N-BENZYLOXYCARBONYL-1,2-DIAMINOETHANE HYDROCHLORIDE
- N-CARBOBENZOXY-1,2-DIAMINOETHANE HYDROCHLORIDE
- N-1-Z-1,2-DIAMINOETHANE HCL
- CAS:
- 18807-71-1
- MF:
- C10H15ClN2O2
- MW:
- 230.69
- Product Categories:
-
- Protected Amines
- Bifunctional Crosslinkers
- Building Blocks
- Chemical Biology
- Chemical Synthesis
- Linkers
- Nitrogen Compounds
- Organic Building Blocks
- Peptide Chemistry
- N-Cbz-diaminoalkanes
- Monoprotected Diaminoalkanes
- Mol File:
- 18807-71-1.mol
BENZYL N-(2-AMINOETHYL)CARBAMATE HYDROCHLORIDE Chemical Properties
- Melting point:
- 169-172 °C(lit.)
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- Water Solubility
- Soluble in water
- solubility
- DMSO (Slightly), Methanol (Slightly)
- form
- Solution Product May Develop Some Turbidity or Precipitate
- color
- Slightly yellow to brown
- BRN
- 4724532
MSDS
- Language:English Provider:SigmaAldrich
BENZYL N-(2-AMINOETHYL)CARBAMATE HYDROCHLORIDE Usage And Synthesis
Chemical Properties
White crystalline powder
Uses
N-(Benzyloxycarbonyl)ethylenediamine Hydrochloride is a reagent used to synthesize new opioid ligand as an analgesics with mixed agonist and antagonist properties to induce tolerance and dependence.
reaction suitability
reagent type: cross-linking reagent
Synthesis
77153-05-0
18807-71-1
General procedure for the synthesis of N-benzyloxycarbonyl ethylenediamine hydrochloride from N-Cbz-N'-Boc-ethylenediamine: benzyl tert-butyl ethane-1,2-dicarbamate (1.5 g, 6.3 mmol) was dissolved in methanol (10 mL) and HCl/EtOAc solution (2 mL) was added. The reaction mixture was stirred at room temperature for 10 h. After removal of the solvent by concentration, N-benzyloxycarbonyl ethylenediamine hydrochloride (1.0 g, 85% yield) was obtained.
References
[1] Bulletin of the Chemical Society of Japan, 1998, vol. 71, # 3, p. 699 - 709
[2] Journal of Peptide Science, 2013, vol. 19, # 1, p. 9 - 15
[3] Patent: WO2015/81282, 2015, A1. Location in patent: Paragraph 00712; 00713
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BENZYL N-(2-AMINOETHYL)CARBAMATE HYDROCHLORIDE(18807-71-1)Related Product Information
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