138124-71-7

Basic information

• Product Name: t-4-<(benzyloxy)methyl>-r-1,2-epoxycyclohexane
• Synonyms: t-4-<(benzyloxy)methyl>-r-1,2-epoxycyclohexane
• CAS NO: 138124-71-7
• Molecular Weight: 218.296
• Mol File: 138124-71-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: t-4-<(benzyloxy)methyl>-r-1,2-epoxycyclohexane(CAS DataBase Reference)
• NIST Chemistry Reference: t-4-<(benzyloxy)methyl>-r-1,2-epoxycyclohexane(138124-71-7)
• EPA Substance Registry System: t-4-<(benzyloxy)methyl>-r-1,2-epoxycyclohexane(138124-71-7)

Safety Data

• Hazardous Substances Data: 138124-71-7(Hazardous Substances Data)

Upstream product

• 138008-16-9 ((1S,2S,5R)-5-Benzyloxymethyl-2-chloro-cyclohexyloxy)-trimethyl-silane 
• 1630-01-9 cis-3,4-Epoxycyclohexanecarboxylic acid methyl ester 
• 76704-23-9 t-3,4-epoxy-r-1-cyclohexanecarboxylic acid 
• 145827-23-2 4-<(benzyloxy)methyl>cyclohexene 
• 100-39-0 benzyl bromide 
• 72581-32-9 cyclohex-3-enylmethanol 
• 138258-88-5 t-5-<(benzyloxy)methyl>-c-2-chloro-r-1-cyclohexanol 
• 91108-46-2 t-3,4-epoxy-r-1-cyclohexanemethanol 

Downstream Products

• 137946-43-1 trans-3-<(benzyloxy)methyl>-1-cyclohexanol 
• 137946-42-0 trans-4-(benzyloxymethyl)cyclohexanol 
• 138258-88-5 t-5-<(benzyloxy)methyl>-c-2-chloro-r-1-cyclohexanol 
• 137946-36-2 (1R,2R,4R)-4-Benzyloxymethyl-2-chloro-cyclohexanol 
• 138008-12-5 t-5-<(benzyloxy)methyl>-t-2-methoxy-r-1-cyclohexanol 
• 138124-72-8 c-4-<(benzyloxy)methyl>-t-2-methoxyy-r-1-cyclohexanol 
• 137265-57-7 (1R,2R,4R)-4-Benzyloxymethyl-2-methoxy-cyclohexanol 

Relevant articles and documents

Regiochemical Control of the Ring-Opening of 1,2-Epoxides by Means of Chelating Processes. 2. Synthesis and Reactions of the cis- and trans-Oxides of 4-cyclohexene, 3-Cyclohexenemethanol, and Methyl 3-Cyclohexenecarboxylate

The synthesis of the diastereoisomeric epoxides cis-1b-d and trans-2b-d and the products of their ring-opening by various nucleophiles are described.The results of the ring-openings of the trans-epoxides 2b-d can be rationalized by combining stereoelectro