CAS 23357-52-0

(S)-(+)-1,2,3,4-tetrahydro-1-naphthylamine

Description:

(S)-(+)-1,2,3,4-tetrahydro-1-naphthylamine is an organic compound characterized by its bicyclic structure, which consists of a naphthalene ring fused with a saturated cyclohexane-like system. This compound features a chiral center, resulting in its designation as (S)-(+), indicating its specific stereochemistry. It is typically a colorless to pale yellow liquid or solid, depending on the temperature and purity. The presence of the amine functional group contributes to its basicity and potential reactivity, allowing it to participate in various chemical reactions, such as nucleophilic substitutions or coupling reactions. This compound is of interest in the field of medicinal chemistry and organic synthesis, often serving as an intermediate in the production of pharmaceuticals or agrochemicals. Its solubility properties can vary, generally being soluble in organic solvents while having limited solubility in water. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken due to potential toxicity or reactivity.

Formula: C₁₀H₁₃N

InChI: InChI=1/C10H13N.ClH/c11-10-7-3-5-8-4-1-2-6-9(8)10;/h1-2,4,6,10H,3,5,7,11H2;1H/t10-;/m0./s1

InChI key: InChIKey=JRZGPXSSNPTNMA-JTQLQIEISA-N

SMILES: N[C@@H]1C=2C(CCC1)=CC=CC2

Synonyms:

• (+)-1,2,3,4-Tetrahydro-1-naphthylamine
• (+)-1-Aminotetralin
• (1S)-1,2,3,4-Tetrahydro-1-naphthalenamine
• (1S)-1,2,3,4-Tetrahydro-1-naphthalenylamine
• (1S)-1,2,3,4-Tetrahydronaphthalen-1-Amine Hydrochloride
• (1S)-1,2,3,4-Tetrahydronaphthalen-1-amine
• (S)-(+)-1,2,3,4-Tetrahydro-1-aminonaphthalene
• (S)-(+)-1-Aminotetraline
• (S)-(-)-1-Aminotetralin
• (S)-(1,2,3,4-Tetrahydro-Naphthalen-1-Yl)Amine
• (S)-1,2,3,4-Tetrahydro-1-naphthalenamine
• (S)-1,2,3,4-Tetrahydronaphthalen-1-Amine
• (S)-1,2,3,4-Tetrahydronaphthalen-1-ylamine
• (S)-1-Amino-1,2,3,4-Tetrahydronaphthalene
• 1-Naphthalenamine, 1,2,3,4-tetrahydro-, (1S)-
• 1-Naphthalenamine, 1,2,3,4-tetrahydro-, (S)-
• 1-Naphthylamine, 1,2,3,4-tetrahydro-, (S)-(+)-
• (S)-1,2,3,4-Tetrahydro-1-Naphthylamine
• (S)-(+)-1,2,3,4-Tetrahydro-1-Naphthylamine
• (S)-1,2,3,4-tetrahydronaphthalen-1-amine hydrochloride
• (s)-(+)-1-aminotetralin tm
• (S)-(+)-1,2,3,4-TETRAHYDRO-1-NAPHTHYLAMINE, CHIPROS 99+%, EE
• (S)-(+)-1,2,3,4-TETRAHYDRO-1-NAPHTHYLAMINE: CHIPROS 99%, EE 99%

(S)-(+)-1,2,3,4-Tetrahydro-1-naphthylamine

CAS: 23357-52-0

Formula: C₁₀H₁₃N

Purity: >98.0%(GC)(T)

Color and Shape: Colorless to Red to Green clear liquid

Molecular weight: 147.22

Ref: 3B-T2878

(S)-(+)-1,2,3,4-Tetrahydro-1-naphthylamine, ChiPros™ 99+%, ee 99%

CAS: 23357-52-0

(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 -transaminase using an enzyme-membrane reactor. This Thermo Scientific Chemicals brand p

Formula: C₁₀H₁₃N

Purity: 99%

Color and Shape: Clear colorless to pale yellow, Liquid

Molecular weight: 147.22

Ref: 02-L17022

(S)-1,2,3,4-Tetrahydronaphthalen-1-amine

CAS: 23357-52-0

Formula: C₁₀H₁₃N

Purity: 95%

Color and Shape: Liquid

Molecular weight: 147.2169

Ref: IN-DA003CFN

(1S)-(+)-1-Amino-1,2,3,4-tetrahydronaphthalene

CAS: 23357-52-0

(1S)-(+)-1-Amino-1,2,3,4-tetrahydronaphthalene

Formula: C₁₀H₁₃N

Purity: 97%

Color and Shape: yellow liquid

Molecular weight: 147.22g/mol

Ref: 54-OR40592

(S)-1-Amino-1,2,3,4-tetrahydro-naphthalene

CAS: 23357-52-0

Formula: C₁₀H₁₃N

Purity: 95%

Color and Shape: Liquid

Molecular weight: 147.221

Ref: 10-F048221

S-(+)-1-Aminotetrahydronaphthalene

CAS: 23357-52-0

S-(+)-1-Aminotetrahydronaphthalene is an amido derivative that is the enantiomer of S-(-)-1-amino-N,N'-diphenylformamide. It has been shown to have anti-obesity effects in mice by increasing energy expenditure and reducing food intake. S-(+)-1-Aminotetrahydronaphthalene also inhibits the release of fatty acids from adipose tissue, which may be due to its ability to suppress lipolysis. The molecular mechanism for these effects is not yet known, but it is thought that the amide group on this compound interacts with certain protein surfaces and steric interactions are involved in its activity.

Formula: C₁₀H₁₃N

Purity: Min. 95%

Molecular weight: 147.22 g/mol

Ref: 3D-FA17854