185019-15-2

Basic information

• Product Name: 3-Nonanol
• CAS NO: 185019-15-2
• Molecular Formula: C9H20O
• Molecular Weight: 144.257
• Mol File: 185019-15-2.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: 3-Nonanol(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Nonanol(185019-15-2)
• EPA Substance Registry System: 3-Nonanol(185019-15-2)

Safety Data

• Hazardous Substances Data: 185019-15-2(Hazardous Substances Data)

Upstream product

• 3839-31-4 dimethyl(phenyl)silyllithium 
• 2984-50-1 1,2-Epoxyoctane 
• 21964-44-3 non-1-en-3-ol 
• 111-84-2 nonane 
• 111-71-7 heptanal 
• 75-24-1 trimethylaluminum 
• 54583-22-1 1-hydroxy-2-bromooctane 
• 676-58-4 methylmagnesium chloride 

Downstream Products

• 20237-46-1 cis-3-nonene 
• 20063-92-7 (E)-3-nonene 
• 6434-78-2 2-nonene 
• 25234-31-5 4-ethyldecanoic acid 
• 65950-02-9 S-p-toluenesulfonic acid-1-ethylheptyl ester 
• 139199-71-6 (3S)-nonan-3-yl (2R)-3,3,3-trifluoro-2-methoxy-2-phenylpropanoate 
• 139199-72-7 (3S)-nonan-3-yl (2R)-3,3,3-trifluoro-2-methoxy-2-phenylpropanoate 
• 1346758-18-6 1-ethylheptyl 3,5-dibromobenzoate 
• 711027-63-3 3-ethylnonanoic acid 
• 60826-15-5 nonan-3-yl acetate 
• 61925-49-3 (S)-nonan-3-ol 
• 61925-50-6 (R)-3-nonanol 
• 925-78-0 3-nonanone 
• 20012-44-6 (1-ethylhexyl)oxybenzene 

Relevant articles and documents

Stereospecific internal almylation of terminal γ,δ-epoxy acrylates

The alkylation of ethyl (S)- and (R)-4,5-epoxy-2-pentenoates (11) and (12), chiral terminal γ,δ-epoxy acrylates prepared from D-mannitol, by trialkylaluminum in the presence of water occurs rcgioselectively at the γ position, i.e., at the internal position, to yield a sole product respectively with net inversion of configuration. The method provides useful chiral synthons for natural product synthesis.

ALKANE OXIDATION BY MODIFIED HYDROXYLASES

This invention relates to modified hydroxylases. The invention further relates to cells expressing such modified hydroxylases and methods of producing hydroxylated alkanes by contacting a suitable substrate with such cells.

Titanocene-catalyzed regiodivergent epoxide openings

The first regiodivergent opening of unbiased epoxides providing the ring-opened products in high enantiomeric excess from racemic and exceptionally high enantiomeric excess from enantioenriched substrates in a double asymmetric process has been devised. It constitutes a more general case of the very important enantioselective openings of meso-epoxides. Copyright