63547-53-5

Basic information

• Product Name: Silane, [(2,6-dimethyl-1-cyclohexen-1-yl)oxy]trimethyl-
• CAS NO: 63547-53-5
• Molecular Formula: C11H22OSi
• Molecular Weight: 198.381
• Mol File: 63547-53-5.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: Silane, [(2,6-dimethyl-1-cyclohexen-1-yl)oxy]trimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Silane, [(2,6-dimethyl-1-cyclohexen-1-yl)oxy]trimethyl-(63547-53-5)
• EPA Substance Registry System: Silane, [(2,6-dimethyl-1-cyclohexen-1-yl)oxy]trimethyl-(63547-53-5)

Safety Data

• Hazardous Substances Data: 63547-53-5(Hazardous Substances Data)

Upstream product

• 2816-57-1 2,6-dimethylcyclohexanone 
• 75-77-4 chloro-trimethyl-silane 
• 16029-98-4 trimethylsilyl iodide 
• 7449-74-3 N-methyl-N-trimethylsilylacetamide 

Downstream Products

• 91966-12-0 β-(1,3-Dimethyl-2-oxo-cyclohexyl)-propionsaeure 
• 124604-64-4 2,6-dimethyl-2-(3,3-diphenyl-2-propenyl)cyclohexanone 
• 4071-74-3 2,6-dimethyl-2-(3-oxobutyl)cyclohexanone 
• 55234-03-2 2-bromo-2,6-dimethyl-cyclohexanone 
• 109125-20-4 2,6-dimethyl-2-iodo-1-cyclohexane 
• 2408-37-9 2,2,6-trimethylcyclohexan-1-one 
• 1361414-54-1 2-(2,6-dimethyl-6-ethenylcyclohex-1-enyl)acetic acid 
• 40790-56-5 2,6-dimethyl-2-cyclohexen-1-one 
• 4071-63-0 rac-4a,8-dimethyl-3,4,4a,5,6,7,8-heptahydronaphthalen-2-one 
• 256487-36-2 2,6-Dimethyl-2-[2-(2,5,5-trimethyl-[1,3]dioxan-2-yl)-ethyl]-cyclohexanone 
• 256487-37-3 2-[2-(1,3-Dimethyl-2-methylene-cyclohexyl)-ethyl]-2,5,5-trimethyl-[1,3]dioxane 

Relevant articles and documents

Diastereoselective Synthesis of (±)-Epianastrephin, (±)-Anastrephin and Analogs Thereof

A process for the synthesis of trans-fused γ-lactones having Formula (IV) from substituted cyclic ketones having Formula (I). A diastereoselective synthesis of (±)-epianastrephin (1) (wherein: R1 is ethenyl, R2 and R3 is methyl, and n is 1), (±)-anastrephin (2) (wherein: R2 is ethenyl, R1 and R3 is methyl and n is 1), and analogs thereof (wherein: R1 is H, C1-5 alkyl, C2-6 alkenyl or C2-6 alkynyl, R2 is H, C1-5 alkyl, C2-6 alkenyl or C2-6 alkynyl, R1 and R2 together with the carbon atom they are attached form a C3-6 cycloalkyl ring, R3 is C1-5 alkyl and n is 0-2):

Silazanes/catalytic bases: Mild, powerful and chemoselective agents for the preparation of enol silyl ethers from ketones and aldehydes

We have developed an efficient method for the preparation of enol silyl ethers using novel agents, silazanes together with NaH or DBU catalyst, wherein TMS and TBDMS groups were smoothly and chemoselectively introduced into ketones and aldehydes under mil

A Total Synthesis of the Sesquiterpene Quinone Metachromin-A

The first total synthesis of the marine natural product metachromin A was accomplished through a convergent synthesis amenable to the preparation of synthetic analogues.The main features of this synthesis are the introduction the oxygenation at C17 employing a Thiele acetoxylation reaction and a stereoselective Horner-Wadsworth-Emmons coupling of a nonstabilized phosphonate with a methyl ketone derivative to generate the required (E)-trisubstituted double bond.