| Identification | Back Directory | [Name]
3,4-Dibenzyloxyphenethylamine hydrochloride | [CAS]
1699-56-5 | [Synonyms]
1699-56-5
(4-Chloro-3-Nitrophenyl)(cy
3,4-DibenzyloxyphenethylamineHCl
3,4-(DIBENZYLOXY)PHENETHYLAMINE HYDROCHLORIDE
3,4-bis(benzyloxy)phenethylamine hydrochloride
(4-CHLORO-3-NITROPHENYL)(CYCLOPROPYL)METHANONE
3,4-DIBENZYLOXYPHENETHYLAMINE HYDROCHLORIDE 98%
3,4-(Dibenzyloxy)phenethylamine hydrochloride,98%
2-(3,4-Bis(benzyloxy)phenyl)ethanaMine hydrochloride
3,4-Dibenzyloxyphenethylamine hydrochloride, HPLC 98% | [EINECS(EC#)]
216-924-4 | [Molecular Formula]
C22H24ClNO2 | [MDL Number]
MFCD00012629 | [MOL File]
1699-56-5.mol | [Molecular Weight]
369.88 |
| Chemical Properties | Back Directory | [Appearance]
beige powder | [Melting point ]
131-133 °C(lit.)
| [InChI]
1S/C22H23NO2.ClH/c23-14-13-18-11-12-21(24-16-19-7-3-1-4-8-19)22(15-18)25-17-20-9-5-2-6-10-20;/h1-12,15H,13-14,16-17,23H2;1H | [InChIKey]
KXIZXPRLNNDQKS-UHFFFAOYSA-N | [SMILES]
Cl.NCCc1ccc(OCc2ccccc2)c(OCc3ccccc3)c1 |
| Hazard Information | Back Directory | [Chemical Properties]
beige powder | [Uses]
3,4-Dibenzyloxyphenethylamine hydrochloride was used in the synthesis of tetrahydroisoquinoline derivatives containing 4(hexylureido)benzenesulfonamide, human β3 adrenergic receptor agonist. It was used as reagent in synthesis of the prodrugs of dopamine. |
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