31503-10-3

Basic information

• Product Name: (1S,2S,3S,4S)-4,7,7-Trimethyl-3-phenyl-bicyclo[2.2.1]heptan-2-ol
• CAS NO: 31503-10-3
• Molecular Weight: 230.35
• Mol File: 31503-10-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (1S,2S,3S,4S)-4,7,7-Trimethyl-3-phenyl-bicyclo[2.2.1]heptan-2-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,2S,3S,4S)-4,7,7-Trimethyl-3-phenyl-bicyclo[2.2.1]heptan-2-ol(31503-10-3)
• EPA Substance Registry System: (1S,2S,3S,4S)-4,7,7-Trimethyl-3-phenyl-bicyclo[2.2.1]heptan-2-ol(31503-10-3)

Safety Data

• Hazardous Substances Data: 31503-10-3(Hazardous Substances Data)

Upstream product

• 464-49-3 (1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one 
• 7070-09-9 (1R,4R)-1,7,7-trimethyl-2-phenylbicyclo[2.2.1]hept-2-ene 
• 31503-04-5 Phenylborneol 

Downstream Products

• 30557-98-3 (+)-(1R,4S)-exo-2-phenylbornan-3-one 
• 30557-98-3 (-)-(1R,2S)-2-endo-phenylbornan-3-one 
• 31503-13-6 (1S,2S,3R,4S)-4,7,7-Trimethyl-3-phenyl-bicyclo[2.2.1]heptan-2-ol 
• 31503-14-7 (1S,2R,3S,4S)-4,7,7-Trimethyl-3-phenyl-bicyclo[2.2.1]heptan-2-ol 
• 31503-12-5 2exo-Phenylbornan-3-on 
• 32663-28-8 2-endo-Phenyl-bornan-3-on 

Relevant articles and documents

THE OCTANT RULE XXIII. ANTIOCTANT EFFECTS IN γ,δ-UNSATURATED KETONES

The exo and endo α-benzyl derivatives (1 and 2. respectively) of (+)-camphor have been synthesized and are found to exert a strong influence on the circular dichroism n?* Cotton effects: 1: Δε301max -0.36 (n-heptane) and 2: Δε302max +3.22, relative to camphor: Δε304max + 1.8 (n-heptane).Evidence for electric dipole transition moment coupling in these γ,δ-unsaturated systems is found in the n?* UV: 1: ε291max 84 (n-heptane) and 2: ε285max 303, relative to camphor: ε290max 25.