Basic information Safety Supplier Related

2-(BENZYLOXY)-1-ETHANAMINE HYDROCHLORIDE

Basic information Safety Supplier Related

2-(BENZYLOXY)-1-ETHANAMINE HYDROCHLORIDE Basic information

Product Name:
2-(BENZYLOXY)-1-ETHANAMINE HYDROCHLORIDE
Synonyms:
  • AMINOETHYLBENZYL ETHER HYDROCHLORIDE
  • 2-(BENZYLOXY)-1-ETHANAMINE HYDROCHLORIDE
  • 2-(Benzyloxy)-1-ethaneamineHCl
  • 2-(Benzyloxy)-1-ethaneaminehydrochloride
  • Aminoethylbenzyl ether hydrochloride 90%
  • Aminoethylbenzyletherhydrochloride90%
  • 2-(benzyloxy)ethanamine hydrochloride
  • 2-(benzyloxy)ethan-1-amine hydrochloride
CAS:
10578-75-3
MF:
C9H14ClNO
MW:
187.67
Product Categories:
  • Phenyls & Phenyl-Het
  • Phenyls & Phenyl-Het
Mol File:
10578-75-3.mol
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2-(BENZYLOXY)-1-ETHANAMINE HYDROCHLORIDE Chemical Properties

Melting point:
142 °C
storage temp. 
Sealed in dry,Room Temperature
form 
liquid
color 
Colorless
InChI
InChI=1S/C9H13NO.ClH/c10-6-7-11-8-9-4-2-1-3-5-9;/h1-5H,6-8,10H2;1H
InChIKey
AFQMWBUNDONXED-UHFFFAOYSA-N
SMILES
C(C1C=CC=CC=1)OCCN.Cl
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
22-36-43
Safety Statements 
26-36
Hazard Note 
Harmful
HazardClass 
IRRITANT
HS Code 
2922390090
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2-(BENZYLOXY)-1-ETHANAMINE HYDROCHLORIDE Usage And Synthesis

Uses

2-Benzyloxyethylamine Hydrochloride is used to synthesize single and double-chain fluorocarbon and hydrocarbon galactosyl amphiphiles with anti-HIV-1 activities.

Synthesis

634925-24-9

10578-75-3

General procedure for the synthesis of 2-benzyloxyethylamine hydrochloride from the compound (CAS: 634925-24-9): to a solution of ether (10 mL) of the product obtained in step 2 (4 g, 15.93 mmol) was slowly added an ether solution (20 mL) of 4N HCl. The reaction mixture was stirred at room temperature overnight. Upon completion of the reaction, the mixture was filtered and the filter cake was washed with hexane. Subsequently, the product was dried under vacuum to afford 2-benzyloxyethylamine hydrochloride in the form of an off-white solid (2 g, 83% yield). The structure of the product was confirmed by 1H-NMR (400 MHz, DMSO-d6): δ 3.01 (t, J = 5.20 Hz, 2H), 3.63 (t, J = 5.60 Hz, 2H), 4.54 (s, 2H), 7.35-7.36 (m, 5H), 8.01 (bs, 3H).

References

[1] Patent: WO2015/27021, 2015, A1. Location in patent: Page/Page column 87 ;88
[2] Carbohydrate Research, 2000, vol. 327, # 3, p. 223 - 260
[3] Patent: US2004/10007, 2004, A1. Location in patent: Page 64-65; 82

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