120925-50-0

Basic information

• Product Name: 1-Octanol, 2-methyl-, (R)-
• CAS NO: 120925-50-0
• Molecular Formula: C9H20O
• Molecular Weight: 144.257
• Mol File: 120925-50-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-Octanol, 2-methyl-, (R)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Octanol, 2-methyl-, (R)-(120925-50-0)
• EPA Substance Registry System: 1-Octanol, 2-methyl-, (R)-(120925-50-0)

Safety Data

• Hazardous Substances Data: 120925-50-0(Hazardous Substances Data)

Upstream product

• 72748-99-3 (R)-1-Amino-2-(methoxymethyl)pyrrolidine 
• 1159491-82-3 4-({[(2R)-2-methyloctyl]oxy}carbonyl)benzoic acid 

Downstream Products

• 170691-34-6 (R)-(-)-ethyl 4-(1-methylheptyloxy)-3-nitrobenzoate 
• 170691-63-1 (R)-(-)-1-(1-methylheptyloxy)-2-nitrobenzene 
• 144808-74-2 (R)-(-)-1-bromo-3-fluoro-4-(1-methylheptyloxy)benzene 
• 1269425-15-1 methyl 2-[(2E,4E)-4,6-dimethyldodeca-2,4-dienamido]-3-(4-t-butyldimethylsilyloxyphenyl)-propanoate 
• 229334-21-8 Gymnastatin H 
• 117184-53-9 aranorosin 
• 117184-53-9 Aranorosin 
• 117184-53-9 Aranorosin 
• 153152-86-4 Ethyl (2S,2'E,4'E,6'R)-2-(4,6-dimethyldodeca-2,4-dienoylamido)-3-(4-hydroxyphenyl)propanoate 
• 153077-13-5 (2E,4E)-(R)-4,6-Dimethyl-dodeca-2,4-dienoic acid [(S)-1-formyl-2-(4-hydroxy-phenyl)-ethyl]-amide 
• 254435-73-9 (7R,9RS,11S)-7,11-dimethyl-9-phenylsulfonylheptadecane 
• 254435-72-8 (7R,9RS,11R)-7,11-dimethyl-9-phenylsulfonylheptadecane 
• 328547-80-4 (5S,7RS,9R)-5,9-dimethyl-7-(phenylsulfonyl)pentadecane 
• 328547-78-0 (5R,7RS,9R)-5,9-dimethyl-7-(phenylsulfonyl)pentadecane 

Relevant articles and documents

Cotonoates A and B, new aromatic esters from Cotoneaster racemiflora

Phytochemical investigation of the chloroform soluble fraction of the methanolic extract of Cotoneaster racemiflora resulted in the isolation of two new aromatic esters named cotonoates A (1) and B (2) along with the known compound methyl 3,4-dihydroxy-5-methoxybenzoate (3). The structures of the new compounds have been assigned on the basis of spectral analysis including ID and 2D NMR techniques. Compound 3 shows significant antioxidant and lipoxygenase inhibitory activities.