Benzyl N-(2-aminoethyl)carbamate hydrochloride

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Benzyl N-(2-aminoethyl)carbamate hydrochloride manufacturers

Benzyl N-(2-aminoethyl)carbamate hydrochloride Basic information

Product Name:	Benzyl N-(2-aminoethyl)carbamate hydrochloride
Synonyms:	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;N-(2-AMINOETHYL)CARBAMIC ACID BENZYL ESTER HYDROCHLORIDE
CAS:	18807-71-1
MF:	C10H15ClN2O2
MW:	230.69
EINECS:
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
InChI	1S/C10H14N2O2.ClH/c11-6-7-12-10(13)14-8-9-4-2-1-3-5-9;/h1-5H,6-8,11H2,(H,12,13);1H
InChIKey	QMLKQXIAPAAIEJ-UHFFFAOYSA-N
SMILES	[H]Cl.NCCNC(OCC1=CC=CC=C1)=O

Safety Information

MSDS Information

Provider	Language
SigmaAldrich	English

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

Benzyl N-(2-aminoethyl)carbamate hydrochloride Preparation Products And Raw materials

Raw materials

Tag:Benzyl N-(2-aminoethyl)carbamate hydrochloride(18807-71-1) Related Product Information

2-Aminoethylammonium chloride Ethylenediamine Ethylenediamine dihydrochloride N-Cbz-1,2-diaMinoethane Z-Phe-Arg-4m-betana HCl Z-Arg-AMC HCl Z-Gly-Gly-Arg-4m-betana HCl Z-Gly-Gly-Arg-betana HCl Z-Arg-4m-betana HCl N-Cbz-Phe-Arg 7-amido-4-methylcoumarin hydrochloride Z-Gly-Gly-Arg-7-amino-4-methylcoumarin Z-Gly-Pro-Arg-AMC HCl N-alpha-Cbz-Arg-Arg 7-amido-4-methylcoumarin hydrochloride Chymotrypsin Substrate II, Fluorogenic CATHEPSIN B SUBSTRATE I, COLORIMETRIC Z-Arg-PNA HCl Z-Gly-Gly-Phe-chloromethylketone Z-Phe-Val-Arg-PNA HCl