120710-98-7

Basic information

• Product Name: Benzenepropanol, g,4-dimethyl-a-(2-methyl-1-propen-1-yl)-, (aR,gS)-
• Synonyms: Benzenepropanol,g,4-dimethyl-a-(2-methyl-1-propenyl)-, (aR,gS)- (9CI); Benzenepropanol, g,4-dimethyl-a-(2-methyl-1-propenyl)-,[R-(R*,S*)]-; (+)-Bisacumol; (7S,9R)-(+)-Bisacumol; Bisacumol
• CAS NO: 120710-98-7
• Molecular Formula: C15H22 O
• Molecular Weight: 218.339
• Mol File: 120710-98-7.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 331.1±11.0 °C(Predicted)
• Density: 0.950±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Benzenepropanol, g,4-dimethyl-a-(2-methyl-1-propen-1-yl)-, (aR,gS)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenepropanol, g,4-dimethyl-a-(2-methyl-1-propen-1-yl)-, (aR,gS)-(120710-98-7)
• EPA Substance Registry System: Benzenepropanol, g,4-dimethyl-a-(2-methyl-1-propen-1-yl)-, (aR,gS)-(120710-98-7)

Safety Data

• Hazardous Substances Data: 120710-98-7(Hazardous Substances Data)

Upstream product

• 1178560-59-2 (7S)-bisacumol acetate 
• 127214-85-1 bisacurone B 
• 122091-54-7 (R)-(+)-2-(4-methylphenyl)propanol 
• 1195-32-0 1-methyl-4-isopropenylbenzene 
• 107-86-8 3,3-dimethyl acrylaldehyde 
• 503543-30-4 (R)-1-(1-bromopropan-2-yl)-4-methylbenzene 
• 532-65-0 (+)-(S)-ar-turmerone 

Downstream Products

• 120681-86-9 4-Bromo-benzoic acid (S)-3-methyl-1-((S)-2-p-tolyl-propyl)-but-2-enyl ester 
• 120681-85-8 4-Bromo-benzoic acid (R)-3-methyl-1-((S)-2-p-tolyl-propyl)-but-2-enyl ester 
• 532-65-0 (+)-(S)-ar-turmerone 
• 1214287-50-9 (+)-(7S,9S)-dihydro-ar-turmerol 
• 1214287-51-0 (+)-(7S,9R)-dihydro-ar-turmerol 
• 4179-21-9 (+)-(S)-dihydro-ar-curcumene 

Relevant articles and documents

Acetylcholinesterase inhibitory activity of volatile oil from peltophorum dasyrachis kurz ex bakar (Yellow Batai) and bisabolane-type sesquiterpenoids

In this study, the chemical compositions and acetylcholinesterase (AChE) inhibitory activitiy of the volatile oil from the bark of Peltophorum dasyrachis Kurz ex Bakar (yellow batai) were evaluated. As a result, 68 compounds, accounting for 88.0% of the t

Total asymmetric synthesis of (7S,9R)-(+)-bisacumol

A facile stereoselective synthetic route to (7S,9R)-(+)-bisacumol 1 has been achieved. This novel approach derives its asymmetry by employing asymmetric dihydroxylation and CBS reduction processes. The resulting sesquiterpene 1 was produced with highly enantio- and diastereoselectivity.