(S)-(+)-1,2,3,4-Tetrahydro-1-naphthylamin, ChiPros™ 99+ %, ee 99 %, Thermo Scientific Chemicals
(S)-(+)-1,2,3,4-Tetrahydro-1-naphthylamin, ChiPros™ 99+ %, ee 99 %, Thermo Scientific Chemicals
(S)-(+)-1,2,3,4-Tetrahydro-1-naphthylamin, ChiPros™ 99+ %, ee 99 %, Thermo Scientific Chemicals
Thermo Scientific Chemicals

(S)-(+)-1,2,3,4-Tetrahydro-1-naphthylamin, ChiPros™ 99+ %, ee 99 %, Thermo Scientific Chemicals

CAS: 23357-52-0 | C10H13N | 147.221 g/mol
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Katalognummer L17022.03
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Chemikalien-Kennzeichnungen
CAS23357-52-0
IUPAC Name1,2,3,4-tetrahydronaphthalen-1-amine
Molecular FormulaC10H13N
InChI KeyJRZGPXSSNPTNMA-UHFFFAOYNA-N
SMILESNC1CCCC2=CC=CC=C12
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SpecificationsSpecification SheetDatenblatt
Appearance (Color)Clear colorless to pale yellow
FormLiquid
Assay (GC)≥99.0%
Enantiomeric excess≥99.0%
Optical Rotation41? ± 1.5? (neat)
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(S)-(+)-1,2,3,4-Tetrahydro-1-naphthylamine is used as a chiral amine derivative used in studies of real-time chiral discrimination of enantiomers as well as in studies of kinetic resolution of chiral amines with ω-transaminase using an enzyme-membrane reactor.

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.

Anwendungen
(S)-(+)-1,2,3,4-Tetrahydro-1-Naphthylamin wird als chirales Amin-Derivat verwendet, das in Studien zur chiralen Diskriminierung von Enantiomeren in Echtzeit sowie in Studien zur kinetischen Auflösung chiraler Amine mit ω-Transaminase mit einem Enzym-Membranreaktor verwendet wird.

Löslichkeit
Wasserlöslich.

Hinweise
Luftempfindlich. Behälter dicht verschlossen lassen. Kühl und trocken in einem gut versiegelten Behälter lagern.
RUO – Research Use Only

Allgemeine Referenzen:

  1. Yunmi Lee.; Amir H. Hoveyda. Efficient Boron-Copper Additions to Aryl-Substituted Alkenes Promoted by NHC-Based Catalysts. Enantioselective Cu-Catalyzed Hydroboration Reactions. J. Am. Chem. Soc. 2009, 131 (9), 3160-3161.
  2. Cathleen M. Crudden.; Yonek B. Hleba.; Austin C. Chen. Regio- and Enantiocontrol in the Room-Temperature Hydroboration of Vinyl Arenes with Pinacol Borane. J. Am. Chem. Soc. 2004, 126 (30), 9200-9201.