52708-03-9

Basic information

• Product Name: 4-Nonanol, (S)-
• Synonyms: 4-Nonanol, (S)-;(S)-8-Methyl-4-octanol;[S,(+)]-4-Nonanol
• CAS NO: 52708-03-9
• Molecular Formula: 52708-03-9
• Molecular Weight: 144.25
• Mol File: 52708-03-9.mol
• Article Data: 5

Chemical Properties

• Melting Point: 6.15°C (estimate)
• Boiling Point: 192.9°C (estimate)
• Flash Point: 79.5°C
• Appearance: /
• Density: 0.8282
• Refractive Index: 1.4197
• PKA: 15.44±0.20(Predicted)
• CAS DataBase Reference: 4-Nonanol, (S)-(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Nonanol, (S)-(52708-03-9)
• EPA Substance Registry System: 4-Nonanol, (S)-(52708-03-9)

Safety Data

• Hazardous Substances Data: 52708-03-9(Hazardous Substances Data)

Upstream product

• 5932-79-6 Propyl-pentyl-carbinol 
• 52708-04-0 (+)-(4S,6Ξ)-6-bromo-nonan-4-ol 
• 20810-18-8 1-nonyn-4-ol 
• 35192-73-5 (R)-non-1-en-4-ol 
• 102919-59-5 trans-5-nonen-1-yn-4-ol 
• 36685-06-0 (4S,6S)-4,6-nonanediol 
• 208656-71-7 (+)-(4S,5R)-5-chloro-4-nonanol 
• 208656-70-6 (-)-(4S,5S)-5-chloro-4-nonanol 
• 935701-22-7 cis-(3S,4R)-3,4-epoxynonane 
• 935866-08-3 (2S,3R)-2,3-epoxyoct-1-yl tosylate 
• 26001-58-1 (Z)-oct-2-en-1-ol 
• 628-71-7 1-Heptyne 
• 20739-58-6 2-octyn-1-ol 
• 39910-26-4 1-diazopentan-2-one 

Relevant articles and documents

The Solvent Effects on the Optical Rotatory Properties of 1,7-Diaryl-5-hydroxy-3-heptanones and Related Compounds

The ORD and CD curves of (S)-1,7-diphenyl-5-hydroxy-3-heptanone, (S)-1,7-bis(3,4-dimethoxyphenyl)-5-hydroxy-3-heptanone, and related model compounds were obtained in selected solvents with different polarity.Causing the 1,7-diaryl-5-hydroxy-3-heptanones d

Chemoenzymatic synthesis of α-halogeno-3-octanol and 4- or 5-nonanols. Application to the preparation of chiral epoxides

A study of the microbiological reduction of different α- halogenoketones (4-chloro-3-octanone, 4-chloro-5-nonanone, 5-bromo-4-nonanone and 5-chloro-4-nonanone) with several strains of microorganism showed great difficulty in reducing ketone functions located in the middle of carbon chains. However, by choosing the appropriate microorganism, several enantiomerically pure diastereoisomers of the corresponding halohydrins have been obtained and were transformed into chiral epoxides.

Chiral Allenylboronic Esters: A Practical Reagent for Enantioselective Carbon-Carbon Bond Formation

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