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

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

CAS: 23357-52-0 | C10H13N | 147.221 g/mol
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Número de catálogoCantidad
L17022.14
también denominado L17022-14
25 g
Número de catálogo L17022.14
también denominado L17022-14
Precio (USD)
-
Cantidad:
25 g
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Identificadores químicos
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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EspecificacionesSpecification SheetHoja de especificaciones
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.

Aplicaciones
La (S)-(+)-1,2,3,4-tetrahidro-1-naftilamina se utiliza como un derivado de la amina quiral utilizado en estudios de discriminación quiral en tiempo real de enantiómeros, así como en estudios de resolución cinética de aminas quirales con ω-transaminasa utilizando un reactor de membrana enzimático.

Solubilidad
Soluble en agua.

Notas
Sensible al aire. Mantener el recipiente herméticamente cerrado. Almacenar en un lugar fresco y seco y en recipientes bien sellados.
RUO – Research Use Only

General References:

  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.