13293-47-5

Basic information

• Product Name: (+)-ISOPINOCAMPHEYLAMINE
• Synonyms: (1S,2S,3S,5R)-(+)-ISOPINOCAMPHEYLAMINE,97% (1S,2S,3S,5R)-(+)-ISOPINOCAMPHEYLAMINE,95%;(+)-ISOPINOCAMPHEYLAMINE 96+% (GC SUM OF ENANTIOMERS);(1S,2S,3S,5R)-3-Pinanamine;(+)-Isopinocampheylamine, (1S,2S,3S,5R)-3-Pinanamine;(1S,2S,3S,5R)-(+)-Isopinocampheylamine 95%
• CAS NO: 13293-47-5
• Molecular Formula: C₁₀H₁₉N
• Molecular Weight: 153.26456
• Mol File: 13293-47-5.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 90 °C18 mm Hg(lit.)
• Flash Point: 160 °F
• Appearance: /
• Density: 0.909 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.556mmHg at 25°C
• Refractive Index: n20/D 1.481(lit.)
• CAS DataBase Reference: (+)-ISOPINOCAMPHEYLAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: (+)-ISOPINOCAMPHEYLAMINE(13293-47-5)
• EPA Substance Registry System: (+)-ISOPINOCAMPHEYLAMINE(13293-47-5)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26
• RIDADR: NA 1993 / PGIII
• WGK Germany: 3
• Hazardous Substances Data: 13293-47-5(Hazardous Substances Data)

Usage

Uses

(1S,2S,3S,5R)-(+)-isopinocampheylamine is a primary bicyclic amine with potent M2 ion channel inhibitor ability similar to that of amantadine, making it a promising candidate for developing anti-influenza agents.

InChI:InChI=1/C10H19N/c1-6-8-4-7(5-9(6)11)10(8,2)3/h6-9H,4-5,11H2,1-3H3/t6-,7+,8-,9-/m0/s1

Upstream product

• 112246-73-8 B-chlorodiisopinocampheylborane 

Downstream Products

• 79-92-5 camphene 
• 98-55-5 terpineol 
• 4057-31-2 1,3,3-trimethylbicyclo<2.2.1>heptan-2-endo-yl acetate 
• 80-26-2 terpinyl acetate 
• 76-49-3 isobornyl acetate 
• 138-86-3 limonene. 
• 1009093-71-3 C₂₆H₃₇IN₂O₆ 
• 1009092-69-6 C₂₇H₃₉IN₂O₅ 
• 1009092-70-9 C₂₈H₄₄IN₃O₅ 
• 1009093-70-2 C₂₇H₄₁IN₂O₇ 
• 1009092-68-5 C₃₃H₅₃IN₂O₅Si 
• 1009093-72-4 C₃₀H₄₆IN₃O₆ 
• 1009092-88-9 C₃₄H₄₅FN₆O₆ 
• 1009092-71-0 C₃₇H₅₄N₄O₇ 

Relevant articles and documents

Organoboranes for synthesis. 16. A convenient synthesis of enantiomerically pure isopinocampheylamine, a chiral derivatizing agent for gas chromatographic analysis of optically active carboxylic acids

Both isomers of enantiomerically pure isopinocampheylamine (1) have been synthesized from the corresponding B-chlorodiisopinocampheylborane by treatment with either methylmagnesium bromide or trimethylaluminum to form B-methyldiisopinocampheylborane, followed by treatment of the intermediate with hydroxylamine-O-sulfonic acid. Application of 1 as a derivatizing agent for the gas chromatographic analysis of optically active carboxylic acids has been demonstrated.