23153-74-4

Basic information

• Product Name: (1,4-DIOXA-SPIRO[4.4]NON-6-YL)-METHANOL
• Synonyms: (1,4-DIOXA-SPIRO[4.4]NON-6-YL)-METHANOL;1,4-Dioxaspiro[4.4]nonane-6-methanol;(1,4-dioxaspiro[4.4]nonan-6-yl)methanol
• CAS NO: 23153-74-4
• Molecular Formula: C₈H₁₄O₃
• Molecular Weight: 158.2
• Mol File: 23153-74-4.mol
• Article Data: 18

Chemical Properties

• Boiling Point: 265 ºC
• Flash Point: 130 ºC
• Appearance: /
• Density: 1.17
• Vapor Pressure: 0.001mmHg at 25°C
• Refractive Index: 1.506
• Storage Temp.: 2-8°C
• PKA: 15.02±0.10(Predicted)
• CAS DataBase Reference: (1,4-DIOXA-SPIRO[4.4]NON-6-YL)-METHANOL(CAS DataBase Reference)
• NIST Chemistry Reference: (1,4-DIOXA-SPIRO[4.4]NON-6-YL)-METHANOL(23153-74-4)
• EPA Substance Registry System: (1,4-DIOXA-SPIRO[4.4]NON-6-YL)-METHANOL(23153-74-4)

Safety Data

• Hazardous Substances Data: 23153-74-4(Hazardous Substances Data)

Usage

General Description

(1,4-DIOXA-SPIRO[4.4]NON-6-YL)-METHANOL is a chemical compound that has a spiro ring system with a substituted methanol group. (1,4-DIOXA-SPIRO[4.4]NON-6-YL)-METHANOL may have applications in organic synthesis and material science due to its unique structure and potential reactivity. It is important for researchers and scientists to study the physical and chemical properties of this compound in order to understand its potential uses and risks. Further research is needed to fully understand the properties and potential applications of (1,4-DIOXA-SPIRO[4.4]NON-6-YL)-METHANOL.

InChI:InChI=1/C8H14O3/c9-6-7-2-1-3-8(7)10-4-5-11-8/h7,9H,1-6H2

Upstream product

• 20618-42-2 2-(hydroxymethyl)cyclopentanone 
• 107-21-1 ethylene glycol 
• 23153-73-3 ethyl 1,4-dioxaspiro[4,4]nonane-6-carboxylate 
• 7757-82-6 sodium sulfate 
• 611-10-9 2-ethoxycarbonyl-1-cyclopentanone 
• 10472-24-9 methyl 2-oxocyclopentane-1-carboxylate 
• 120-92-3 cyclopentanone 
• 110295-58-4 1,4-dioxa-spiro[4.4]nonane-6-carboxylic acid methyl ester 

Downstream Products

• 20618-42-2 2-(hydroxymethyl)cyclopentanone 
• 116802-67-6 2-(1H-imidazol-1-ylmethyl)cyclopentan-1-on 
• 62138-01-6 (+/-)-(1α,2α,3β,5β)-3-amino-5-(hydroxymethyl)-1,2-cyclopentanediol 
• 76909-91-6 rel-(1R,5R)-5-(hydroxymethyl)cyclopent-2-en-1-ol 
• 132591-69-6 5-(4-Chloro-phenylselanylmethyl)-spiro[3.4]octane 
• 132591-65-2 2-(4-Chloro-phenylselanylmethyl)-cyclopentanone 
• 132591-63-0 6-(4-Chloro-phenylselanylmethyl)-1,4-dioxa-spiro[4.4]nonane 
• 132591-67-4 5-(4-Chloro-phenylselanylmethyl)-spiro[3.4]octan-1-one 
• 68755-19-1 trans-2-hydroxycyclopentanemethanol cyclic phosphoric acid phenyl ester 
• 88733-69-1 6-benzyloxymethyl-1,4-dioxaspiro[4,4]nonane 
• 130733-88-9 2-(((tert-butyldiphenylsilyl)oxy)methyl)cyclopentan-1-one 
• 131923-99-4 (E)-6-Phenyl-hex-5-enoic acid 2-hydroxy-ethyl ester 

Relevant articles and documents

Synthetic studies directed toward the total synthesis of a jatrophane diterpene

Jatrophane diterpenes are of significant biological importance as they have shown a remarkable potential as a Pgp inhibitor. These diterpenes have a characteristic framework. Synthesis of an advanced synthon was achieved in high yielding steps. The methyl

SPIROHYDANTOIN COMPOUNDS AND THEIR USE AS SELECTIVE ANDROGEN RECEPTOR MODULATORS

The present invention relates to a compound of formula (1-1 ) in free form or in pharmaceutically acceptable salt form in which the substituents are as defined in the specification; to its preparation, to its use as a medicament and to medicaments comprising it. The present invention further provides a combination of pharmacologically active agents and a pharmaceutical composition.

Benzimidazole compound

An object of the present invention is to provide a novel chemical compound useful as a therapeutic or prophylactic agent for acid-related diseases, having an excellent inhibitory effect against gastric acid secretion, an excellent effect of maintaining the inhibitory effect against gastric acid secretion, thereby maintaining intragastric pH high for a long time, and having more safety and appropriate physicochemical stability. Provided is a compound represented by where R1 and R3 may be the same or different and each represent a hydrogen atom or a C1-C6 alkyl group; R2 represents (5,5-dimethyl-1,3-dioxan-2-yl)methoxy group, 5,7-dioxaspiro[2.5]oct-6-ylmethoxy group, 1,5,9-trioxaspiro[5.5]undec-3-ylmethoxy group, or (2,2-dimethyl-1,3-dioxan-5-yl)methoxy group; R4, R5, R6 and R7 represent a hydrogen atom, halogen atom, C1-C6 alkyl group, C1-C6 haloalkyl group, C1-C6 alkoxy group or C1-C6 haloalkoxy group; and W1 represents a single bond, methylene or ethylene group, a salt thereof or a solvate of these.