62141-26-8

Basic information

• Product Name: (1,4-DIOXA-SPIRO[4.5]DEC-8-YL)-ACETIC ACID ETHYL ESTER
• Synonyms: (1,4-DIOXA-SPIRO[4.5]DEC-8-YL)-ACETIC ACID ETHYL ESTER;ethyl 2-(1,4-dioxaspiro[4.5]decan-8-yl)acetate;1,4-Dioxaspiro[4.5]decane-8-acetic acid, ethyl ester;Ethyl 1,4-dioxaspiro[4.5]decane-8-acetate;(1,4-DIOXA-SPIRO[4.5]DEC-8-YL)-ACETIC ACID ETHYL ESTER-25;Ethyl 2-(1,4-dioxaspiro[4.5]dec-8-yl)acetate
• CAS NO: 62141-26-8
• Molecular Formula: C₁₂H₂₀O₄
• Molecular Weight: 228.28
• Product Categories: Miscellaneous
• Mol File: 62141-26-8.mol
• Article Data: 41

Chemical Properties

• Boiling Point: 308.4±17.0 °C(Predicted)
• Appearance: /
• Density: 1.10±0.1 g/cm3(Predicted)
• CAS DataBase Reference: (1,4-DIOXA-SPIRO[4.5]DEC-8-YL)-ACETIC ACID ETHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: (1,4-DIOXA-SPIRO[4.5]DEC-8-YL)-ACETIC ACID ETHYL ESTER(62141-26-8)
• EPA Substance Registry System: (1,4-DIOXA-SPIRO[4.5]DEC-8-YL)-ACETIC ACID ETHYL ESTER(62141-26-8)

Safety Data

• Hazardous Substances Data: 62141-26-8(Hazardous Substances Data)

Usage

General Description

"(1,4-DIOXA-SPIRO[4.5]DEC-8-YL)-ACETIC ACID ETHYL ESTER" is a chemical compound with the molecular formula C12H18O4. (1,4-DIOXA-SPIRO[4.5]DEC-8-YL)-ACETIC ACID ETHYL ESTER belongs to the class of organic compounds known as carboxylic acid esters, which are esters formed from a carboxylic acid and an alcohol. The presence of the dioxa-spirodecane moiety in the structure of this compound makes it unique. It is commonly used as a flavoring agent and as a fragrance ingredient in various consumer products. Additionally, it is utilized in the production of perfumes, soaps, and cleaning products. However, it is important to handle this chemical with caution, as it may cause irritation to the skin, eyes, and respiratory system upon exposure.

Upstream product

• 51656-91-8 ethyl 1,4-dioxaspiro[4,5]dec-8-ylideneacetate 
• 4746-97-8 cyclohexanedione monoethylene ketal 
• 867-13-0 diethoxyphosphoryl-acetic acid ethyl ester 

Downstream Products

• 135761-76-1 2-(1,4-dioxaspiro[4.5]decan-8-yl)ethanol 
• 204245-53-4 2-(1,4-dioxaspiro[4,5]dec-8-yl)-1-(4-phenyl-1-piperazinyl)ethanone 
• 317338-52-6 4-(1H-imidazol-5-ylmethyl)cyclohexanone 
• 869501-11-1 4-(4-hydroxycyclohexylmethyl)imidazole-1-carboxylic acid tert-butyl ester 
• 869501-10-0 4-(4-oxocyclohexylmethyl)imidazole-1-carboxylic acid tert-butyl ester 
• 869501-12-2 4-(4-aminocyclohexylmethyl)imidazole-1-carboxylic acid tert-butyl ester 
• 869501-03-1 4-(1H-imidazol-5-ylmethyl)cyclohexylamine dihidrobromide 
• 1292321-59-5 C₂₂H₂₇F₂N₃O₃S 
• 1292321-58-4 C₂₂H₂₅F₅N₂O₃S 
• 1292321-32-4 C₂₀H₃₀F₂N₂O₂ 
• 1292321-57-3 C₂₁H₂₇F₂N₃O₂S 
• 1292321-56-2 C₂₂H₂₅F₂N₃O₂S 
• 1292321-55-1 C₂₂H₂₅F₂N₃O₂S 
• 1292322-02-1 C₁₉H₂₈F₂N₂O 

Relevant articles and documents

Harnessing Additional Capability from in Water Reaction Conditions: Aldol versus Knoevenagel Chemoselectivity

Aldol reaction chemoselectivity, racemic or enantioselective, has not been previously demonstrated in the presence of Knoevenagel active functional groups. Here, we show that unhindered β-diketones remain unreacted while a ketone moiety undergoes a highly

INHIBITORS OF INDOLEAMINE 2,3-DIOXYGENASE AND METHODS OF THEIR USE

There are disclosed compounds that modulate or inhibit the enzymatic activity of indoleamine 2,3 -dioxygenase (IDO), pharmaceutical compositions containing said compounds and methods of treating proliferative disorders, such as cancer, viral infections and/or inflammatory disorders utilizing the compounds of the invention.

INHIBITORS OF INDOLEAMINE 2,3-DIOXYGENASE AND METHODS OF THEIR USE

There are disclosed compounds that modulate or inhibit the enzymatic activity of indoleamine 2,3-dioxygenase (IDO), pharmaceutical compositions containing said compounds and methods of treating proliferative disorders, such as cancer, viral infections and/or inflammatory disorders utilizing the compounds of the invention.