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Thermo Scientific Chemicals
2-(4-Bromophenyl)ethylamine, 98%
CAS: 73918-56-6 | C8H11BrN | 201.09 g/mol
化学物質識別子
CAS73918-56-6
IUPAC Name2-(4-bromophenyl)ethan-1-aminium
Molecular FormulaC8H11BrN
InChI KeyZSZCXAOQVBEPME-UHFFFAOYSA-O
SMILES[NH3+]CCC1=CC=C(Br)C=C1
さらに表示
仕様
スペックシート
スペックシートAssay (GC)>97.5%
4-Bromophenethylamine was used in the synthesis of pyrazinoisoquinoline derivatives and N-2-(4-bromophenyl)ethyl chloroacetamide. It was also used in the synthesis of alkyl arylamino sufides employing elemental sulfur and various halides.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
4-Bromophenethylamine was used in the synthesis of pyrazinoisoquinoline derivatives and N-2-(4-bromophenyl)ethyl chloroacetamide. It was also used in the synthesis of alkyl arylamino sufides employing elemental sulfur and various halides.
Solubility
Slightly soluble in water.
Notes
Refrigerate. Keep container tightly closed in a dry and well-ventilated place. Store away from oxidizing agent.
4-Bromophenethylamine was used in the synthesis of pyrazinoisoquinoline derivatives and N-2-(4-bromophenyl)ethyl chloroacetamide. It was also used in the synthesis of alkyl arylamino sufides employing elemental sulfur and various halides.
Solubility
Slightly soluble in water.
Notes
Refrigerate. Keep container tightly closed in a dry and well-ventilated place. Store away from oxidizing agent.
RUO – Research Use Only
General References:
- Kim JH, et al. Formation of pyrazinoisoquinoline ring system by the tandem amidoalkylation and N-acyliminium ion cyclization: An efficient synthesis of Praziquantel. Tetrahedron. 1998, 54(26), 7395-7400.
- Jungyeob Ham; Sung Jin Cho; Jaeyoung Ko; Jungwook Chin; Heonjoong Kang. A facile one-pot preparation of alkyl aminoaryl sulfides for the synthesis of GW7647 as an agonist of peroxisome proliferator-activated receptor alpha. Journal of Organic Chemistry. 2006, 71(15), 5781-5784.