121099-13-6

Basic information

• Product Name: Cyclohexaneacetic acid, a-hydroxy-, methyl ester, (S)-
• CAS NO: 121099-13-6
• Molecular Formula: C9H16O3
• Molecular Weight: 172.224
• Mol File: 121099-13-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Cyclohexaneacetic acid, a-hydroxy-, methyl ester, (S)-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexaneacetic acid, a-hydroxy-, methyl ester, (S)-(121099-13-6)
• EPA Substance Registry System: Cyclohexaneacetic acid, a-hydroxy-, methyl ester, (S)-(121099-13-6)

Safety Data

• Hazardous Substances Data: 121099-13-6(Hazardous Substances Data)

Upstream product

• 143100-57-6 (S)-Cyclohexyl-(4-methoxy-phenoxy)-acetic acid 
• 139040-44-1 (R)-2,2,2-Trichloro-1-cyclohexyl-ethanol 
• 139040-39-4 1,1,1-trichloro(cyclohexyl)ethan-2-one 
• 67-56-1 methanol 
• 61475-31-8 (S)-hexahydromandelic acid 
• 74-88-4 methyl iodide 
• 143100-59-8 (S)-Cyclohexyl-(4-methoxy-phenoxy)-acetic acid methyl ester 
• 62783-63-5 cyclohexyl-oxo-acetic acid methyl ester 
• 186581-53-3 diazomethane 

Downstream Products

• 300578-00-1 (S)-Cyclohexyl-((2R,3S)-3-phenylselanyl-tetrahydro-furan-2-yloxy)-acetic acid methyl ester 

Relevant articles and documents

Stereoselective Protonation of Carbanions, 4. Enantioselective Protonation of Lactone Enolates

The prochiral lithium enolates derived from the five-membered lactones rac-1 and rac-2 were protonated by 37 OH- and 21 NH-chiral proton sources in THF at -78 deg C.The enantioselectivities, determined directly from the reaction mixture by chiral HPLC, ar

CsF-Promoted Esterification of Carboxylic Acids. A Practical Alternative to the Diazomethane Method and Direct Conversion of Organotin Carboxylates

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STEREOSELECTIVE REDUCTION OF C=X BY A CHIRAL 1,4-DIHYDROPYRIDINE (NADH-MIMIC) IN A SELF-IMMOLATIVE PROCESS

A series of prochiral ketones and a prochiral imine was reduced with high absolute stereoselectivity using an optically active 4-methyl-1,4-dihydropyridine in the presence of Mg(ClO4)2.