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Thermo Scientific Chemicals
(S)-(+)-1,2,3,4-Tetrahydro-1-naphthylamine, ChiPros™ 99+%, ee 99%
CAS: 23357-52-0 | C10H13N | 147.221 g/mol
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Chemical Identifiers
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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Specifications
Specification Sheet
Specification SheetAppearance (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.
Applications
(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.
Solubility
Soluble in water.
Notes
Air Sensitive. Keep container tightly closed. Store in cool, dry conditions in well sealed containers.
(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.
Solubility
Soluble in water.
Notes
Air Sensitive. Keep container tightly closed. Store in cool, dry conditions in well sealed containers.
RUO – Research Use Only
General References:
- 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.
- 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.