54831-51-5

Basic information

• Product Name: Octanoic acid, 4-methyl-, ethyl ester, (.+/-.)-
• Synonyms: Octanoic acid, 4-methyl-, ethyl ester, (.+/-.)-
• CAS NO: 54831-51-5
• Molecular Weight: 0
• Mol File: 54831-51-5.mol
• Article Data: 8

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Octanoic acid, 4-methyl-, ethyl ester, (.+/-.)-(CAS DataBase Reference)
• NIST Chemistry Reference: Octanoic acid, 4-methyl-, ethyl ester, (.+/-.)-(54831-51-5)
• EPA Substance Registry System: Octanoic acid, 4-methyl-, ethyl ester, (.+/-.)-(54831-51-5)

Safety Data

• Hazardous Substances Data: 54831-51-5(Hazardous Substances Data)

Upstream product

• 64-17-5 ethanol 
• 54947-74-9 rac-4-methyloctanoic acid 
• 18589-27-0 2-iodohexane 
• 140-88-5 ethyl acrylate 
• 50965-90-7 2-methylenehexan-1-ol 
• 1070-66-2 2-n-butylacrolein 
• 79909-21-0 ethyl γ-iodovalerate 
• 693-04-9 butyl magnesium bromide 
• 105-53-3 diethyl malonate 
• 171627-80-8 (4S)-Methyloctanal 
• 171627-78-4 (6S)-2,6-Dimethyl-2-decene 
• 67214-54-4 (R)-citronellyl tosylate 
• 1117-61-9 (3R)-citronellol 
• 128342-72-3 (4S)-4-methyloctanoic acid 

Downstream Products

• 17302-27-1 (-)(R)-2.5-dimethyl-nonane 

Relevant articles and documents

Concise asymmetric syntheses of (S)-ethyl 4-methyloctanoate and its acid: Aggregation pheromones of rhinoceros beetles of the genus Oryctes

A concise stereoselective approach to the asymmetric syntheses of (S)-ethyl 4-methyloctanoate and its acid, main aggregation pheromones of the genus Oryctes and an important fragrance compounds, is described. The synthesis utilizes the organocatalyzed Mac

Nickel-catalyzed cross-coupling of non-activated and functionalized alkyl halides with alkyl grignard reagents

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Substrate sorption into the polymer matrix of Novozym 435 and its effect on the enantiomeric ratio determination

In the enantioselective esterification of 4-methyloctanoic acid with ethanol by immobilised Candida antarctica lipase B (Novozym 435), the enantiomeric excesses determined during the course of the reaction deviated strongly from the theoretical values, le