ChemicalBook--->CAS DataBase List--->38336-04-8

38336-04-8

38336-04-8 Structure

38336-04-8 Structure
IdentificationBack Directory
[Name]

2-(BENZYLOXY)-ETHYLAMINE
[CAS]

38336-04-8
[Synonyms]

2-(BENZYLOXY)-ETHYLAMINE
2-Aminoethyl benzyl ether
2-(benzyloxy)-1-ethanamine
2-(benzyloxy)ethan-1-amine
2-(Benzyloxy)ethylamine96%
2-(Benzyloxy)-1-ethaneaMine
2-(Benzyloxy)ethylamine 96%
2-(Phenylmethoxy)ethanamine
2-(benzyloxy)ethanamine 1HCl
Ethanamine, 2-(phenylmethoxy)-
2-(benzyloxy)ethanamine(SALTDATA: HCl)
2-(BENZYLOXY)-ETHYLAMINE ISO 9001:2015 REACH
2-(Phenylmethoxy)ethylamine, 2-Aminoethyl benzyl ether
[Molecular Formula]

C9H13NO
[MDL Number]

MFCD00235180
[MOL File]

38336-04-8.mol
[Molecular Weight]

151.21
Chemical PropertiesBack Directory
[Boiling point ]

241℃
[density ]

1.45
[refractive index ]

1.5260
[Fp ]

85℃
[storage temp. ]

Keep in dark place,Inert atmosphere,2-8°C
[solubility ]

Chloroform (Slightly), DMSO (Slightly)
[form ]

Oil
[pka]

8.82±0.10(Predicted)
[color ]

Colourless to Pale Yellow
[InChI]

InChI=1S/C9H13NO/c10-6-7-11-8-9-4-2-1-3-5-9/h1-5H,6-8,10H2
[InChIKey]

XJGVVOAKITWCAB-UHFFFAOYSA-N
[SMILES]

C(N)COCC1=CC=CC=C1
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)
GHS05
[Signal word ]

Danger
[Hazard statements ]

H314
[Precautionary statements ]

P280-P305+P351+P338-P310
[RIDADR ]

3267
[HazardClass ]

8
[PackingGroup ]

III
[HS Code ]

2921599090
Hazard InformationBack Directory
[Uses]

2-(Benzyloxy)-1-ethanamine (2-(Benzyloxy)ethylamine) is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
[Synthesis Reference(s)]

Tetrahedron Letters, 36, p. 3465, 1995 DOI: 10.1016/0040-4039(95)00527-J
[Synthesis]

1H-Isoindole-1,3(2H)-dione, 2-[2-(phenylmethoxy)ethyl]-

87107-79-7

2-(BENZYLOXY)-ETHYLAMINE

38336-04-8

GENERAL METHOD: Compound (CAS: 87107-79-7) (3 mmol) was dissolved in ethanol (30 mL) at 50 °C, followed by slow addition of 85% hydrazine hydrate (0.19 mL, 3.3 mmol). The reaction temperature was maintained at 50 °C and the reaction mixture was stirred continuously for 4 hours. Upon completion of the reaction, the mixture was cooled to room temperature and the solids were separated by filtration. The filtrate was concentrated under reduced pressure to give the crude product 2-(benzyloxy)ethylamine in 90% yield.

[References]

[1] Bioorganic and Medicinal Chemistry Letters, 2015, vol. 25, # 14, p. 2782 - 2787
[2] Patent: WO2012/64680, 2012, A1. Location in patent: Page/Page column 142
[3] Patent: WO2012/62157, 2012, A1. Location in patent: Page/Page column 142; 143
[4] Patent: US2011/178077, 2011, A1. Location in patent: Page/Page column 14
Spectrum DetailBack Directory
[Spectrum Detail]

2-(BENZYLOXY)-ETHYLAMINE(38336-04-8)1HNMR
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