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ChemicalBook >  Product Catalog >  Organic Chemistry >  Amides >  (R)-(-)-1,2,3,4-Tetrahydro-1-naphthylamine

(R)-(-)-1,2,3,4-Tetrahydro-1-naphthylamine

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(R)-(-)-1,2,3,4-Tetrahydro-1-naphthylamine Basic information

Product Name:
(R)-(-)-1,2,3,4-Tetrahydro-1-naphthylamine
Synonyms:
  • (R)-1,2,3,4-TETRAHYDRONAPHTHALEN-1-AMINE
  • (R)-(1,2,3,4-TETRAHYDRO-NAPHTHALEN-1-YL)AMINE
  • (R)-(-)-1-AMINOTETRALIN
  • (R)-(+)-1-AMINOTETRALIN
  • (R)-1-AMINOTETRALIN
  • (R)-(-)-1-AMINOTETRALINE
  • (R)-1-AMINOTETRALINE
  • (R)-1-Amino-1,2,3,4-tetrahydronaphthalene
CAS:
23357-46-2
MF:
C10H13N
MW:
147.22
EINECS:
628-771-4
Product Categories:
  • Tetrazoles
Mol File:
23357-46-2.mol
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(R)-(-)-1,2,3,4-Tetrahydro-1-naphthylamine Chemical Properties

Melting point:
116-119 °C
Boiling point:
118-120 °C/10 mbar
Density 
1.002 g/mL at 25 °C
refractive index 
1.565
Flash point:
>110°C
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
form 
clear liquid
pka
9.39±0.20(Predicted)
color 
Colorless to Light yellow to Light orange
Water Solubility 
Soluble in water (6.91g/L at 25°C).
Sensitive 
Air Sensitive
BRN 
4231302
InChI
InChI=1S/C10H13N/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-2,4,6,10H,3,5,7,11H2/t10-/m1/s1
InChIKey
JRZGPXSSNPTNMA-SNVBAGLBSA-N
SMILES
[C@H]1(N)C2=C(C=CC=C2)CCC1
CAS DataBase Reference
23357-46-2(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,N,C
Risk Statements 
36/37-51/53-36/37/38-52/53-34-22
Safety Statements 
26-36/37/39-61-45
RIDADR 
UN 3082
WGK Germany 
3
HazardClass 
8
PackingGroup 
HS Code 
2921450090

MSDS

  • Language:English Provider:ALFA
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(R)-(-)-1,2,3,4-Tetrahydro-1-naphthylamine Usage And Synthesis

Uses

(R)-(-)-1,2,3,4-Tetrahydro-1-naphthylamine is a important organic intermediate. It can be used in agrochemical, pharmaceutical and dyestuff field. Chiral amines play an important role in stereoselective organic synthesis. They are used directly as resolving agents, building blocks or chiral auxiliaries.

Synthesis

(R)-1-Amino-1,2,3,4-tetrahydronaphthalene is a contactor that can be synthesized by the reaction of an enantiomerically pure amine with a primary oxidant. 

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