(S)-(-)-1-(4-Fluorophenyl)ethylamine, ChiPros 99%, ee 99%

Name: (S)-(-)-1-(4-Fluorophenyl)ethylamine, ChiPros 99%, ee 99%
SKU: L19121.03

CAS: 66399-30-2 | C8H10FN | 139.173 g/mol

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数量:

1 g

5 g

25 g

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製品番号（カタログ番号） L19121.03

または、製品番号L19121-03

価格（JPY）

数量:

1 g

一括またはカスタム形式をリクエストする

化学物質識別子

CAS66399-30-2

IUPAC Name1-(4-fluorophenyl)ethan-1-amine

Molecular FormulaC8H10FN

InChI KeyQGCLEUGNYRXBMZ-UHFFFAOYNA-N

SMILESCC(N)C1=CC=C(F)C=C1

さらに表示

仕様

スペックシート

FormLiquid

Optical Rotation-33.0? ± 1.0? (neat)

Enantiomeric excess≥98.5%

Appearance (Color)Clear colorless

Assay (GC)≥98.5%

さらに表示

(S)-(-)-1-(4-Fluorophenyl)ethylamine is used in organic synthesis. It acts as a ligand and form a coordination complex, diacetato-2-O-bis[(S)-1-(4-fluorophenyl)ethylamine-N]palladium(II) by reacting with palladium(II) acetate.

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
(S)-(-)-1-(4-Fluorophenyl)ethylamine is used in organic synthesis. It acts as a ligand and form a coordination complex, diacetato-2-O-bis[(S)-1-(4-fluorophenyl)ethylamine-N]palladium(II) by reacting with palladium(II) acetate.

Solubility
Miscible with dimethyl sulfoxide.

Notes
Incompatible with strong oxidizing agents.

RUO – Research Use Only

General References:

Li, G.; Ren, J.; Iwaki, H.; Zhang, D.; Hasegawa, Y.; Wu, Q.; Feng, J.; Lau, P. C. K.; Zhu, D. Substrate profiling of cyclohexylamine oxidase and its mutants reveals new biocatalytic potential in deracemization of racemic amines. Appl. Microbiol. Biotechnol. 2014, 98 (4), 1681-1689.
Qin, J.; Dhondi, P.; Huang, X.; Mandal, M.; Zhao, Z.; Pissarnitski, D.; Zhou, W.; Aslanian, R.; Zhu, Z.; Greenlee, W.; Clader, J.; Zhang, L.; Cohen-Williams, M.; Jones, N.; Hyde, L.; Palani, A. Discovery of fused 5,6-bicyclic heterocycles as gamma-secretase modulators. Bioorg. Med. Chem. Lett. 2011, 21 (2), 664-669.