92829-83-9

Basic information

• Product Name: 8-(benzyloxy)-1,4-dioxaspiro[4.5]decane
• Synonyms: 8-(benzyloxy)-1,4-dioxaspiro[4.5]decane;8-(benzyloxy)-1,4-dioxaspiro[4.5]decane(WXC04704)
• CAS NO: 92829-83-9
• Molecular Formula: C₁₅H₂₀O₃
• Molecular Weight: 248.3175
• Mol File: 92829-83-9.mol
• Article Data: 19

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 8-(benzyloxy)-1,4-dioxaspiro[4.5]decane(CAS DataBase Reference)
• NIST Chemistry Reference: 8-(benzyloxy)-1,4-dioxaspiro[4.5]decane(92829-83-9)
• EPA Substance Registry System: 8-(benzyloxy)-1,4-dioxaspiro[4.5]decane(92829-83-9)

Safety Data

• Hazardous Substances Data: 92829-83-9(Hazardous Substances Data)

Usage

General Description

8-(benzyloxy)-1,4-dioxaspiro[4.5]decane is a chemical compound with a spirocyclic structure and a benzyloxy group attached to the 8-position. It is a bicyclic compound containing a 1,4-dioxaspiro[4.5]decane core, which is a unique and versatile building block in organic synthesis. 8-(benzyloxy)-1,4-dioxaspiro[4.5]decane has the potential for use in medicinal chemistry and drug development, as well as in the creation of new materials and functional molecules. Its spirocyclic structure and unique functional group make it an interesting compound for further study and potential applications in various fields of chemistry and pharmaceutical research.

Upstream product

• 22428-87-1 4,4-ethylenedioxycyclohexan-1-ol 
• 100-39-0 benzyl bromide 
• 4746-97-8 cyclohexanedione monoethylene ketal 
• 69125-55-9 4-hydroxy-1-methoxy-1-cyclohexene 
• 78881-14-8 2-Hydroxy-1-cyclohexanon-ethylenacetal 
• 100-44-7 benzyl chloride 

Downstream Products

• 2987-06-6 4-(benzyloxy)cyclohexanone 
• 350506-81-9 4-(benzyloxy)cyclohex-2-enone 
• 543724-85-2 4-benzyloxy-2-bromo-cyclohex-2-enone 
• 543724-88-5 4-benzyloxy-2-bromo-1-vinyl-cyclohex-2-enol 
• 543724-92-1 acetic acid 4-benzyloxy-2-bromo-1-vinyl-cyclohex-2-enyl ester 
• 543724-95-4 [3-Bromo-4-hept-6-en-(E)-ylidene-cyclohex-2-enyloxymethyl]-benzene 
• 543725-01-5 3-Benzyloxy-6-hept-6-en-(E)-ylidene-cyclohex-1-enecarbaldehyde 
• 73658-17-0 4-Benzyloxy-2-methylene-cyclohexanone 
• 73658-27-2 4-Benzyloxy-1-methyl-2-methylene-cyclohexanol 
• 85221-01-8 3-(5-Benzyloxy-2-methyl-cyclohex-1-enyl)-propan-1-ol 
• 85221-00-7 3-(5-Benzyloxy-2-methyl-cyclohex-1-enyl)-propionaldehyde 
• 92829-88-4 Toluene-4-sulfonic acid 3-(5-benzyloxy-2-methyl-cyclohex-1-enyl)-propyl ester 
• 92829-89-5 [3-(3-Iodo-propyl)-4-methyl-cyclohex-3-enyloxymethyl]-benzene 
• 92844-01-4 3-((3E,7E)-10-Hydroxy-7-methyl-deca-3,7-dienyl)-4-methyl-cyclohex-3-enol 

Relevant articles and documents

EMULSION WITH IMPROVED BIOABSORPTION COMPOSITION COMPRISING CATIONIC POLYESTER COPOLYMER AND HYDROPHOBIC DRUG AND METHOD FOR PREPARING THE SAME

The present invention relates to an emulsion composition with an improved bioabsorption rate containing a cationic polyester-based copolymer, and a poorly soluble drug. The emulsion composition comprises: a cationic polyester-based copolymer including a c

COMPOUNDS USEFUL AS KINASE INHIBITORS

This invention relates to novel compounds. The compounds of the invention are tyrosine kinase inhibitors. Specifically, the compounds of the invention are useful as inhibitors of Bruton's tyrosine kinase (BTK).The invention also contemplates the use of the compounds for treating conditions treatable by the inhibition of Bruton's tyrosine kinase, for example cancer, lymphoma, leukemia and immunological diseases.

Stereoelectronic Model to Explain Highly Stereoselective Reactions of Seven-Membered-Ring Oxocarbenium-Ion Intermediates

Nucleophilic attack on seven-membered-ring oxocarbenium ions is generally highly stereoselective. The preferred mode of nucleophilic attack forms the product in a conformation that minimizes transannular interactions, thus leading to different stereoselectivity as compared to that of reactions involving six-membered-ring oxocarbenium ions.