N-Cbz-1,2-diaMinoethane

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N-Cbz-1,2-diaMinoethane manufacturers

N-Cbz-1,2-diaMinoethane Basic information
Product Name:N-Cbz-1,2-diaMinoethane
Synonyms:N-1-CARBOBENZOXY-1,2-DIAMONOETHANE HYDROCHLORIDE;N-1-Z-1,2-DIAMINOETHANE HCL;N-(2-AMINOETHYL)CARBAMIC ACID BENZYL ESTER HYDROCHLORIDE;N-Cbz-ethylenediamine hydrochloride;benzyl 2-aminoethylcarbamate;(2-AMino-ethyl)-carbaMic acid benzyl ester;Z-NH(CH2)2NH2 HCL;Z-1,2-DIAMINOETHANE HCL
CAS:72080-83-2
MF:C10H14N2O2
MW:194.23
EINECS:
Product Categories:
Mol File:72080-83-2.mol
N-Cbz-1,2-diaMinoethane Structure
N-Cbz-1,2-diaMinoethane Chemical Properties
Melting point 169-172 °C(lit.)
Boiling point 188 °C(Press: 4.5 Torr)
density 1.134±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,2-8°C
pka12.19±0.46(Predicted)
AppearanceColorless to light pink Liquid
InChIInChI=1S/C10H14N2O2/c11-6-7-12-10(13)14-8-9-4-2-1-3-5-9/h1-5H,6-8,11H2,(H,12,13)
InChIKeyQMMFTRJQCCVPCE-UHFFFAOYSA-N
SMILESC(OCC1=CC=CC=C1)(=O)NCCN
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
3
MSDS Information
ProviderLanguage
SigmaAldrich English
N-Cbz-1,2-diaMinoethane Usage And Synthesis
Synthesis
Benzyl chloroformate

501-53-1

Ethylenediamine

107-15-3

N-Cbz-1,2-diaMinoethane

72080-83-2

Dichloromethane (100 mL), ethylenediamine (39 mL, 0.58 mol) and potassium carbonate (32.4 g, 0.23 mol) were added to a 500 mL three-necked flask under nitrogen protection. The temperature of the reaction system was controlled at -5 to 0°C and a solution of benzyl chloroformate (20.0 g, 0.12 mol) in dichloromethane (100 mL) was slowly added dropwise under stirring. The dropwise addition process was completed in about 1 hour, followed by continued stirring of the reaction for 2 hours at room temperature. Upon completion of the reaction, the reaction mixture was washed with water (200 mL x 2). The organic layer was separated and dried over anhydrous sodium sulfate (10 g). The organic layer was concentrated under reduced pressure to give a light yellow foamy product of 23.4 g. To the residue, ethyl acetate (80 mL) was added and stirred at room temperature until completely dissolved, then petroleum ether (80 mL) was added dropwise to precipitate a white solid (N-Cbz-1,2-diaminoethane). The solid was collected by filtration, and the mother liquor was concentrated to obtain 15.1 g of light yellow oil, the total yield was 66.5%.

References[1] Chemical Communications, 2017, vol. 53, # 52, p. 7088 - 7091
[2] New Journal of Chemistry, 2013, vol. 37, # 7, p. 1895 - 1905
[3] ACS Medicinal Chemistry Letters, 2014, vol. 5, # 5, p. 550 - 555
[4] Chemistry - A European Journal, 2011, vol. 17, # 19, p. 5251 - 5255
[5] Synthesis, 1984, # 12, p. 1032 - 1033
Tag:N-Cbz-1,2-diaMinoethane(72080-83-2) Related Product Information
Benzyl N-(2-aminoethyl)carbamate hydrochloride Z-Val-Phe-OH Z-Pro-NH2 Ethylenediamine N-Cbz-Val-Tyr methyl ester Z-Ala-Gly-Gly-OH Z-Ile-Gly-OH Z-Ala-Phe-OH Z-Phe-Pro-NH2 Z-Ile-Phe-OH Z-Pro-D-Leu-OH Z-Val-Ala-OH Z-Pro-Met-OH Z-Tyr-Tyr-OH Z-DL-Ala-Gly-OH Z-Pro-Ile-OH Z-Ile-Ala-OH Z-Leu-Gly-Gly-OH