13309-95-0

Basic information

• Product Name: 1,3-Dioxane,2-(2-methoxyphenyl)-(9CI)
• Synonyms: 1,3-Dioxane,2-(2-methoxyphenyl)-(9CI)
• CAS NO: 13309-95-0
• Molecular Formula: C₁₁H₁₄O₃
• Molecular Weight: 194.22706
• Product Categories: PHENYL
• Mol File: 13309-95-0.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,3-Dioxane,2-(2-methoxyphenyl)-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Dioxane,2-(2-methoxyphenyl)-(9CI)(13309-95-0)
• EPA Substance Registry System: 1,3-Dioxane,2-(2-methoxyphenyl)-(9CI)(13309-95-0)

Safety Data

• Hazardous Substances Data: 13309-95-0(Hazardous Substances Data)

Usage

General Description

1,3-Dioxane,2-(2-methoxyphenyl)-(9CI) is a chemical compound with the molecular formula C9H12O3. It is a cyclic ether with a single oxygen atom in its ring structure. 1,3-Dioxane,2-(2-methoxyphenyl)-(9CI) is also known as 2-Methoxyphenyl 1,3-dioxane and is used in the synthesis of various organic compounds and pharmaceuticals. 1,3-Dioxane,2-(2-methoxyphenyl)-(9CI) is primarily used as an intermediate in the production of other chemicals and does not have many direct consumer applications. It is important to handle and use this compound with caution as it may pose risks to human health and the environment.

Upstream product

• 135-02-4 ortho-anisaldehyde 
• 504-63-2 trimethyleneglycol 

Downstream Products

• 773092-64-1 (3RS,4RS)-3-hydroxy-4-[4-[3-(2-methoxy-benzyloxy)-propoxy]-phenyl]-piperidin-1-carboxylic acid tert-butylester 
• 773092-65-2 4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}-3-oxopiperidine-1-carboxylic acid tert-butyl ester 
• 773092-61-8 toluene-4-sulfonic acid 3-(2-methoxybenzyloxy)propyl ester 
• 773092-62-9 1-(3-iodopropoxymethyl)-2-methoxybenzene 
• 24588-70-3 2-(2'-methoxyphenyl)-1,3-dithiane 

Relevant articles and documents

Acetalization of carbonyl compounds catalyzed by bismuth triflate under solvent-free conditions

Carbonyl compounds were converted to the corresponding 1,3-dioxolanes and 1,3-dioxanes with ethylene glycol and 1,3-propandiol in the presence of bismuth triflate under solvent-free conditions. In addition, high chemoselective protection of aldehydes in the presence of ketones has been achieved.

The discovery and preparation of disubstituted novel amino-aryl-piperidine- based renin inhibitors

Recently, trans-disubstituted oxo-aryl-piperidines have been identified as small molecule nonpeptide renin inhibitors for the modulation of hypertension. Herein, we report on the discovery and preparation of a new class of novel cis-disubstituted amino-aryl-piperidines as a mixture of enantiomers that are potent in vitro renin inhibitors and also, possess in vivo antihypertensive activity in a double transgenic mouse model.

Piperidine derivative rennin inhibitors

Disclosed are piperidine derivatives, their manufacture and use as inhibitors of renin.